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Category:Quality Assurance & Control

OHSE MANAGER A-VILADECAVALLS64960862747650120

OHSE MANAGER A-VILADECAVALLS

MISSION To collaborate with the Plant Management and Corporate in reaching OHSE objectives by implementing and maintaining the OHSE Management System. GENERAL FUNCTIONS Represent OHSE duties to the Plant Committee, and follow the Key Performance Indicators, as well as define improvement programs to meet local and corporate objectives. Lead implementation of Corporate OHSE Management Systems and local procedures and instructions. Plan the identification and the assessment of environmental aspects and hazards. Lead and deploy emergency response. Lead the root\-cause analysis of incidents and their corrective measures. Lead internal, legal and certification audits, including interested parties' requirements, as well as the corrective\-action plans. Lead risks and opportunities analysis with preventive criteria. Identify OHSE training needs inherent to the job position, and provide them to HR. Define and lead awareness campaigns to improve environmental performance and safety behavior. Observe Ficosa’s Code of Ethics to avoid fraudulent practices. Comply with Information Security Management System (ISMS) applicable to the job, along with the training related thereto. Lead the team, guaranteeing its effectiveness, development and motivation, fostering Ficosa's values. Provide the team with the necessary means to comply with OHSE rules, ensuring they are properly used. Actively cooperate in maintaining, promoting and improving the OHSE and Quality department. (\*) The duties described are only the most typical of this position and are in no way a comprehensive list. POSITION REQUIREMENTS **Academic background:** Bachelor’s degree, mainly in Occupational, Health \& Safety or Environmental Sciences **Languages:** Fluent local language \& Advanced English (spoken \& written) **Experience:** Minimum of 5 years in a similar position OTHER SPECIFICATIONS **Additional background :** Master’s degree in Environment or Occupational Health \& Safety would be of additional value **Additional training:** Knowledge of ISO 14\.001 auditor, OHSES 18\.001 auditor or Microsoft Office (word, excel or power point) would be of additional value Ficosa is an equal opportunity employer. We strongly believe that a diverse workforce is key to our success, regardless of gender, nationality, age or others. Our focus is not only on our People, but as well on our Planet: protecting the environment is one of the main targets to which we dedicate all our efforts to develop products and more efficient and sustainable solutions.

Carrer Mirador Montserrat, 2, 08232 Viladecavalls, Barcelona, Spain

Cobol (Porto)64859747224322121

VNG \- Cais de Gaia, VNG \- Lake Towers Cobol (Porto) Cobol Developer Choosing Capgemini means choosing a company where you will be empowered to shape your career in the way you’d like, where you’ll be supported and inspired by a collaborative community of colleagues around the world, and where you’ll be able to reimagine what’s possible. Join us and help the world’s leading organizations unlock the value of technology and build a more sustainable, more inclusive world. YOUR ROLE We are looking for a COBOL programmer to join our team in Porto. In this role, you will be responsible for: * Developing, testing, and implementing COBOL code for banking systems, including transaction processing, account management, and financial reporting. * Collaborating with systems analysts, software architects, and other team members to understand project requirements and ensure the delivery of high\-quality solutions. * Performing analysis and diagnosis of problems in existing systems, proposing and implementing effective solutions. * Participating in code reviews and ensuring compliance with coding standards and best practices. * Collaborating with technical support teams to resolve emergency issues and ensure the stability of production systems. * Staying abreast of software development best practices and technologies relevant to the COBOL environment. YOUR PROFILE* Previous experience in software development using COBOL. * Solid understanding of structured and object\-oriented programming concepts. * Ability to work independently and as part of a team, demonstrating effective communication skills. * Familiarity with relational database management systems, such as DB2\. * Excellent problem\-solving skills and the ability to make decisions under pressure. * Bachelor's degree in Computer Science, Software Engineering, or a related field (or equivalent experience) WHAT WE´LL LOVE ABOUT WORKING HERE?* At Capgemini Portugal we have a flexible and dynamic work environment. Flexibility enables a better work\-life balance and gives more flexibility to the employee to manage the working hours, as well if he works at the office or remotely, according with the company’s hybrid work policy; * We have local programs that promote people growth, reskill and new skills development (Career Acceleration Programs); * We promote an empowering environment with autonomy and peers' relationships among the top scores of our Monthly Employees' feedback; * Next to this, we also offer an attractive compensation package and benefits such as Health and Life insurance, as well as Referral program with bonuses for talent recommendations and other fringe benefits according with our partnerships in force. * Capgemini Portugal is an equal opportunity employer. We promote equality and dignity in all aspects of recruitment and employment, as well as employment offers and promotions made according with competence and ability or performance, respectively. ABOUT CAPGEMINI Capgemini is a global business and technology transformation partner, helping organizations to accelerate their dual transition to a digital and sustainable world, while creating tangible impact for enterprises and society. It is a responsible and diverse group of 340,000 team members in more than 50 countries. With its strong over 55\-year heritage, Capgemini is trusted by its clients to unlock the value of technology to address the entire breadth of their business needs. It delivers end\-to\-end services and solutions leveraging strengths from strategy and design to engineering, all fuelled by its market leading capabilities in AI, cloud and data, combined with its deep industry expertise and partner ecosystem. The Group reported 2023 global revenues of €22\.5 billion. Get the future you want \| www.capgemini.com Apply now! \#LI\-Hybrid Works in the area of Software Engineering, which encompasses the development, maintenance and optimization of software solutions/applications.1\. Applies scientific methods to analyse and solve software engineering problems.2\. He/she is responsible for the development and application of software engineering practice and knowledge, in research, design, development and maintenance.3\. His/her work requires the exercise of original thought and judgement and the ability to supervise the technical and administrative work of other software engineers.4\. The software engineer builds skills and expertise of his/her software engineering discipline to reach standard software engineer skills expectations for the applicable role, as defined in Professional Communities.5\. The software engineer collaborates and acts as team player with other software engineers and stakeholders. Ref. code 333901\-en\_GB Posted on 24 Sep 2025 Experience level Experienced Professionals Contract type Permanent Location VNG \- Cais de Gaia, VNG \- Lake Towers Business unit ABL Southern Central Europe Brand Capgemini Professional communities Software Engineering

WWG6+35 Gaià, Spain

Warehouse Picker/Packer64859242742145122

Warehouse Picker/Packer

We are the new owners of a well\-established wholesale business in the toy/gift industry with a loyal customer base and a strong reputation for quality and service. We’re excited to continue the business’s legacy as we, bringing fresh energy, and new opportunities for growth. This is your opportunity to become part of a vibrant new team from day one and help us shape its future in our new location. We are seeking a Picker Packer to join our new team as we transition into this exciting new chapter. Reporting directly to the Warehouse Manager, you will be responsible for the efficient and organised application of warehousing, inventory, dispatch and receiving activities Key Responsibilities Your main responsibilities in this varied role will include, but are not limited to: Accurately pick and securely pack items for dispatch. Ensure items meet quality standards before dispatch. Assist in inventory counts and report discrepancies. Follow shipping protocols, including labelling and documentation. Follow OH\&S guidelines and use safety equipment. Maintain effective communication within the team. Collaborate with the rest of the team to meet productivity goals. Maintain a clean and organised workspace. Verify stock levels during receiving and dispatch. Restock shelves as needed. The ideal candidate will have: Previous warehouse experience Good time management and organisational skills Ability to prioritise tasks based on urgency Excellent communication skills Computer literacy with MS Office and some experience with inventory management software Ability to handle last\-minute requests and willingness to assist where needed Sharp attention to detail Physical fitness for heavy lifting A driver’s licence A forklift licence Must be able to pass a National Police Check Award – Storage Services and Wholesale Award – Full time, Wholesale employee Level 4 Tipo de puesto: Media jornada Sueldo: 2\.000,00€\-2\.500,00€ al mes Beneficios: * Flexibilidad horaria Ubicación del trabajo: Viajes periódicos

Plaça de l'Ajuntament, 4, 08901 L'Hospitalet de Llobregat, Barcelona, Spain

€ 2,000-2,500/month

HEAD OF LEARNING & DEVELOPMENT64842971539969123

HEAD OF LEARNING & DEVELOPMENT

At Mango, we wear passion in everything we do. Born in Barcelona and present in over 120 countries, we inspire the world with creativity, innovation, and authenticity. Our multicultural team is the engine of our success. We take pride in taking fashion beyond boundaries, connecting our unique style with people across the globe. We are seeking a Head of Learning & Development to lead the transformation and operational excellence of the Learning & Development function by designing and executing its strategy and developing core skills. Align all initiatives within the function with business priorities and deliver an outstanding experience with measurable impact on performance, productivity, and internal mobility, as well as high-quality functional reporting. * Define, lead, and implement the cross-functional Learning & Development strategy, ensuring a scalable learning ecosystem. * Identify and develop upskilling and reskilling strategies for core skills, aligned with business priorities. * Lead the design, rollout, and continuous improvement of development programs and learning pathways for core skills: AI & Digital, Retail, Product, Leadership, as well as pathways for key talent groups such as new managers, pre-leadership profiles, etc. * Continuously update and introduce new L&D programs to support the company’s strategic objectives. * Lead and facilitate workshops and interventions across company functions, both individually and in groups. * Lead and develop the L&D team, raising standards in execution, stakeholder management, and results orientation. * Design and operate the governance model for the function, ensuring effective management of key stakeholders—including People Business Partners and local L&D specialists in other countries. * Collaborate with People Business Partners to gather and analyze current and future needs, design required development plans, and create and implement personalized development plans for key employees. * Drive the operational transformation of L&D through process optimization, AI adoption, integration of methodologies and tools, and change management to ensure successful adoption. * Serve as Key User for Workday Learning (or other HRIS), ensuring data quality, consistency, traceability, and governance of recurring reporting. * Lead planning, monitoring, and tracking of the L&D budget, including reporting and variance control. * Be accountable for the L&D analytics and reporting framework: KPI definition, dashboard development, and conversion of data into actionable decisions. * Identify and establish relationships with vendors to achieve desired outcomes. * Act as an active agent of change, fostering a culture of continuous improvement within the Talent function. ABOUT YOU: * Bachelor’s degree in Business Administration, Psychology, or related field. * Minimum 5 years’ experience in HR functions or HR consulting or change management. * Experience in Learning & Development. * Retail industry experience is a plus. * Analytical mindset, efficiency- and continuous-improvement-oriented, proactive, self-motivated, energetic, with strong communication and influencing skills. * Coaching and facilitation skills. * Motivated to contribute to transforming the L&D function into a more agile, innovative, and high-value-adding area. * Passionate about the People space and enjoy creating impactful learning experiences. * Advanced English proficiency. * Knowledge of Workday and other global talent management systems is a plus. YOUR BENEFITS: * Enjoy a flexible schedule and hybrid work model tailored to your needs. At Mango, we champion work-life balance. * At Mango, the weekend starts on Friday at noon. We offer shortened working hours on Fridays and the day before holidays. * Plan your vacations according to your preferences. At Mango, we value your time and want you to savor every moment. * As part of the Mango team, enjoy discounts across all our product lines—so you’re always on-trend! * Flexible compensation package with tax advantages: private health insurance, training, catering, and childcare program. * Free company transportation from Barcelona and El Vallés. * At Mango, we invest in your personal and professional growth. Access a wide range of training opportunities, personalized mentoring, continuous development programs, and internal promotion paths that will propel you toward success. Technically, you’ll have opportunities to train on various technological platforms, as well as participate in workshops, meetups, communities of practice, team-building activities, and company meetings. * Think big! Mango offers international opportunities across more than 120 markets to broaden your horizons and grow alongside us globally. At Mango, we believe in an inclusive culture where creativity and innovation inspire us to take fashion further. That’s why we are committed to offering equal opportunities to everyone, valuing the authenticity of each individual. Taking Fashion Further

Carrer del Camí Reial, 49, 08184 Palau-solità i Plegamans, Barcelona, Spain

Senior Data Engineer - Evinova64842963220739124

Senior Data Engineer - Evinova

This role is based in **Barcelona**, with an on\-site commitment of three days a week. Fluency in **English** is required. Evinova is a new health tech business with a mission to transform billions of patients’ lives through technology, data, and cutting\-edge ways of working in the Life Sciences industry. Evinova provides a software platform and application suite that focuses on science to support clinical trials by enabling effective data analytics and efficient planning, execution, and oversight of all trials in a sponsor portfolio. Join us to deliver market\-leading digital health solutions that are science\-based, evidence\-led, and human experience\-driven. Be part of a diverse team that pushes the boundaries of science by digitally empowering a deeper understanding of the patients we are helping. Launch game\-changing digital solutions that improve the patient's experience, optimize clinical trial execution, and deliver better health outcomes. **Accountabilities** We are creating a dynamic and innovative team to take our organization to the forefront of technology solutions for the life sciences industry. Our cloud platform will play a crucial part in the success of Evinova as the foundation for our current and future digital products. As an Evinova Senior Data Engineer, you will innovate and develop solutions for moving data throughout the ecosystem from various sources to make the data consumable for applications and components using modern tools and technologies. Key Responsibilities: * Develop and maintain scalable data pipelines for processing datasets. * Design, implement, and optimize data architectures. * Ensure data quality, integrity, and security across systems. * Work with cloud platforms (AWS) to manage data infrastructure. * Optimize ETL processes and ensure efficient data movement. * Monitor and troubleshoot data pipelines to maintain reliability. * Collaborate with data scientists and analysts to support business needs. * Automate workflows and deployment processes for data infrastructure. * Collaborate with other engineering teams to identify and utilize shared services including orchestration, notification, and tracing services. * Remain current with organizational strategy to align solutions with long\-term direction. * Create and maintain comprehensive documentation for the application, services, and database, ensuring transparency and ease of use for both internal teams and potential customers. * Provide direction and review for peer work products. * Mentor other engineers on good coding practice and quality coding techniques. **Essential Skills/Experience** * Bachelor’s or Master’s degree in Computer Science, Data Engineering, or a related field. * 5\+ years of experience in data engineering, software development, or analytics. * Familiarity with AWS cloud development environment and capabilities including Lambda, Glue, Step Functions, EventBridge, and CDK w/Typescript. * Familiarity with Kubernetes clusters and Kafka streams. * Good knowledge of GitHub and CI/CD for data engineering workflows. * Expertise in database systems. * Strong programming skills in Node.js, Python, and TypeScript. Familiarity with Kotlin preferred. * Proficiency in security best practices, data protection, and encryption methods. * Knowledge of data security standards and regulatory compliance in the healthcare and clinical research industry. * Familiarity with technical concepts in infrastructure or applications. * Knowledge of industry good practice and standards such as ISO (multiple), GAMP GxP, ICH GCP, FDA 21 CFR, GDPR, CMMI, ITIL, GDPR. When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life\-changing medicines. In\-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. Ready to make a difference? Apply now!

Carrer del Rosselló, 64, Eixample, 08029 Barcelona, Spain

Incoming Inspector64842315797251125

Incoming Inspector

At Alstom, we understand transport networks and what moves people. From high\-speed trains, metros, monorails, and trams, to turnkey systems, services, infrastructure, signalling and digital mobility, we offer our diverse customers the broadest portfolio in the industry. Every day, 80,000 lead the way to greener and smarter mobility worldwide, connecting cities as we reduce carbon and replace cars. Could you be the full\-time **Incoming Inspector** in **Santa Perpetua de Mogoda (Barcelona)** we’re looking for? The Incoming inspector ensures the compliance of purchased products and parts delivered to the ALSTOM facilities. He / She performs inspections, checks, and follows sampling procedures according to the applicable instructions on products having been delivered by suppliers before their use in production. **Accountabilities \& Authorities:** * Perform inspections according to Incoming Control Plan * Accept or Reject products as defined in the inspection instruction/ checklist * Records inspection results in the digital tools as required * Accurately document Non\-conformity when applicable with clear characterization * Ensure the use of calibrated equipment and instrumentations used in the inspections. * Maintain all controlled document files and test records in a timely and accurate manner. * Assist in the writing and updating inspection procedures, control plan and checklists. **Educational Requirements** **Mandatory:** * Must be able to read drawings (2D and 3D) / specifications and be able to understand 3D geometry * Familiar with a variety of measurement equipment. * Competency to use computer applications **Desirable:** * Associates degree or diploma, technical major preferred. * Qualified on special process of his/her scope of work. * Railway experience a "plus". **Experience** **Mandatory:** * Experience within manufacturing industry * Experience using SAP or similar computer applications **Desirable:** * Quality inspection experience within manufacturing industry. * Experience with typical products used and their defect modes * Experience in Quality / audit are valued **Competencies \& Skills** * Analytical and detail\-oriented * Rigor and process\-oriented * Ease to communicate with business partners * Mechanically or electrically inclined, comfortable using measurement tools * Experience in operational activities, in documentation management \& collaboration and team working. As a global business, we’re an equal\-opportunity employer that celebrates diversity across the 70\+ countries we operate in. We’re committed to creating an inclusive workplace for everyone. **Job Segment:** ERP, SAP, Technology

Carrer de Lluís Millet, 21, 08130 Santa Perpètua de Mogoda, Barcelona, Spain

Industrial Quality Inspector64842315812995126

Industrial Quality Inspector

Req ID:506230 At Alstom, we understand transportation networks and what moves people. From high-speed trains, metros, monorails, and trams to systems, services, infrastructure, signaling, and end-to-end digital mobility solutions, we offer our diverse customers the industry’s broadest portfolio. Every day, 80,000 professionals lead the way toward greener, smarter mobility worldwide—connecting cities while reducing carbon emissions and replacing cars. Could you be the **Industrial Quality Inspector** in **Barcelona** we’re looking for? **Your future role** Take on a new challenge and apply your quality expertise in an innovative field. You’ll work alongside young, proactive colleagues. You’ll be responsible for **conducting inspections and ensuring product quality (including post-rework verification) in accordance with the Quality Control Plan**. On a daily basis, you’ll collaborate closely with teams across the organization (production), **record inspection results in designated tools**, and much more. Specifically, you’ll **support the workshop manager in station-to-station transfer activities and propose quality improvements in collaboration with the workshop manager**. You’ll also perform destructive and non-destructive testing. **All about you** We value passion and attitude above experience. That’s why we don’t expect you to possess all the skills. Instead, we’ve listed some that we believe will help you succeed and grow in this role: * Technical education. * Ability to read technical specifications and drawings, and familiarity with test equipment. * More than four years’ experience in industrial quality inspection. * Rigor and communication skills. * Experience in operational activities, documentation management, and teamwork. **What we offer you** Join us on a transformative lifelong journey: the rail industry is here to stay—giving you opportunities to grow and develop new skills and experiences throughout your career. You’ll also be able to: * Enjoy stability, challenges, and a long-term career free from mundane daily routines. * Work on cutting-edge rolling stock projects. * Collaborate with cross-functional teams and supportive colleagues. * Contribute to innovative projects. * Use our collaborative working environment. * Shape your career in any direction you choose—across all functions and countries. * Benefit from our investment in your development through award-winning learning programs. * Benefit from a fair, dynamic rewards package that recognizes your performance and potential. You don’t need to be a train enthusiast to thrive with us. We guarantee that when you board one of our trains with friends or family, you’ll feel proud. If you’re ready for the challenge, we’d love to hear from you! **Important** As a global company, we provide equal opportunities and celebrate diversity across the 70+ countries where we operate. We are committed to creating an inclusive workplace for everyone.

Carrer de Lluís Millet, 21, 08130 Santa Perpètua de Mogoda, Barcelona, Spain

Sr Biostatistician - Neurology (Europe and LATAM only)64841275637377127

Sr Biostatistician - Neurology (Europe and LATAM only)

**Description** Sr Biostatistician \- Neurology (Europe and LATAM only) Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** * This role is open to Europe (excluding Switzerland) or LATAM (ARG, BRA, COL, MEX) * Please submit all CVs in English * Previous clinical trial lead experience within Neurology within industry is required Serves as a statistical department resource, mentors biostatisticians on job skills, and oversees or develops training plans or materials for Biostatistics associates. Conducts training sessions, or otherwise trains new hires and enhance the skills of existing personnel.  Directs the activities of other biostatistics personnel on assigned projects to ensure timely completion of high quality work. Provides independent review of project work produced by other biostatisticians in the department.  Provides support across all statistical tasks during the lifecycle of the project, from protocol to CSR.  Prepares or oversees the preparation of Statistical Analysis Plans (SAPs), including development of well\-presented mock\-up displays for tables, listings, and figures. Collaborates with sponsor, if required.  May be responsible as Lead Biostatician for the statistical aspects of the protocol, generation of randomization schedule, and input to the clinical study report.  Creates or reviews programming specifications for analysis datasets, tables, listings, and figures.  Reviews SAS annotated case report forms (CRFs), database design, and other study documentation to ensure protocol criteria are met and all data is captured as required to support a high quality database and the planned analysis.  Implements company objectives, and creates alternative solutions to address business and operational challenges.  As biostatistics representative on project teams, interfaces with other departmental project team representatives  Preparing in advance for internal meetings, contributing ideas, and demonstrating respect for opinions of others Conducts and participates in verification and quality control of project deliverables, ensuring that output meets the expected results and is consistent with analysis described in the SAP and specifications.  May lead complex or multiple projects (e.g. submissions, integrated analyses), and attend regulatory agency meetings or responds to questions, as needed, to support the statistical analysis results of clinical trials on behalf of the sponsor.  Manages scheduling and time constraints across multiple projects, sets goals based on priorities from management, discusses time estimates for completion of study related activities with biostatistics management, adapts to timeline or priority changes by reorganizing daily workload, and proactively communicates to biostatistics management any difficulties with meeting these timelines.  Monitors progress on study activities against agreed upon milestones and ensures the study timelines for project deliverables are met. Identifies out of scope tasks and escalates to management.  Provides statistical programming support as needed.  May participate in Data Safety Monitoring Board (DSMB) and/or Data Monitoring Committee (DMC) activities, including charter development and serving as an independent non\-voting biostatistician. May serve as a voting statistician on DSMBs and/or DMCs.  Provides input and reviews, and subsequently follows applicable SOPs, WIs, and relevant regulatory guidelines (e.g. ICH).  Maintains well organized, complete, and up\-to\-date project documentation, and verification/quality control documents and programs; ensuring inspection readiness.  Displays willingness to work with others and assists with projects and initiatives as necessary to meet the needs of the business.  Prepares in advance for internal meetings, contributes ideas, and demonstrates respect for opinions of others  Supports business development activities by contributing to proposals, budgets, and attending sponsor bid defense meetings.  Performs other work\-related duties as assigned.  Minimal travel may be required. **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Sr or Principal Biostatistician \- Neurology

Carrer del Rosselló, 64, Eixample, 08029 Barcelona, Spain

Senior Project Specialist (Sponsor Dedicated) The Netherlands64841245276929128

Senior Project Specialist (Sponsor Dedicated) The Netherlands

**Description** Senior Project Specialist (Sponsor Dedicated) The Netherlands Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full\-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: **WORK HERE MATTERS EVERYWHERE** Why Syneos Health * We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. * We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. * We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong. **Job Responsibilities** * Set\-up, maintain and/or close out project files and study information ((e.g., regulatory documents, Trial Master File (TMF), enrollment, Adverse Events (AEs)/Serious Adverse Events (SAEs), site supplies, Institutional Review Board re\-approvals, data queries) on a variety of databases and systems. * Attends, participates, prepares and distributes meeting minutes and action items for both internal and external meetings (sponsor, trusted process, functional, investigator meetings). Follows up with team members on action items to closure. * Maintains timely and effective communication among team members and site staff. Keeps Project Leadership and Clinical Research Associates (CRAs) fully apprised of sites and study status. May contact site staff as needed for critical information. * Provide administrative support to Project Leads and functional leads. * Ensure all study documents are archived based on the appropriate guidelines and policy. * Provide support for quality assurance activities, including preparation for audits and internal review, prepare documentation and follow through to resolution on actionable issues. Qualifications: * Associates Degree (or equivalent) level of qualification in life sciences, Medicine, Pharmacy, Nursing or related field or equivalent combination of education and experience * Knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory requirements. * Strong organizational skills. * Ability to manage time and work independently. * High proficiency with full MS Office Applications. * Strong communication, presentation, interpersonal skills, both written and spoken, with an ability to inform, influence, convince, and persuade * Ability to travel if necessary preferred (approximately 5%) * High level of competence in English language **Get to know Syneos Health** Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000\+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever\-changing environment. Learn more about Syneos Health. http://www.syneoshealth.com **Additional Information** Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. **Summary** Roles within Clinical Project Management job family areesponsible for planning, directing, creating and communicating clinical study time\-lines. Gathers input from cross\-functional teams and creates plans that help the team produce deliverables on schedule. Ensures consistency of clinical study and processes across clinical trials, overseeing and resolving operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations such as site and vendor selection, preparing clinical trial budgets. Ensures studies are conducted within clinical trial protocols, monitoring progress and following up with team members and line managers when issues develop. Implements and prepares the clinical development strategy as outlined by the clinical teams. May develop trial recruitment strategies.Impact and ContributionIndividual contributors who provide organizational related support or service (administrative or clerical), as well as roles operating in support of daily business activities (e.g., technical, production, or craft levels). The majority of time is spent in the delivery of support services or activities, typically under supervision. Roles do not typically require advanced education or training. Established and experienced support individual contributor. Work consists of tasks that are typically routine, with some deviation from standard practice. Requires broad knowledge of operational systems and practices typically gained through extensive experience and/or education.

Carrer del Rosselló, 64, Eixample, 08029 Barcelona, Spain

Senior Nutrition Manager64841233562243129

Senior Nutrition Manager

At **GBfoods** we offer culinary solutions in several countries of **Europe** and **Africa** with prestigious leading local brands, including **Jumbo, Gallina Blanca, Erasco, Gino, Liebig, Star, Bama, D\&L, Grand'Italia and Blå Band**, among others. Our Purpose **“Celebrating local flavours”** is to empower and take care of each of the local communities we belong to and to bring out their authentic flavours. Some of our local brands have been in consumers' kitchens for over a century and have positioned themselves as authentically loved brands, as well as deeply rooted parts of the local culture. Today, with a turnover of **around 1,4 billion euros** and a team of around **3\.600 people**, we are the preferred choice of millions of consumers. **Job description:** The Nutrition Senior Manager is responsible for shaping and driving the company’s nutrition agenda in alignment with strategic business goals. This role bridges nutritional science with corporate strategy, ensuring that product development, regulatory compliance, and consumer engagement are informed by robust nutritional insights and market trends. **Role \& Responsibilities**: **Strategic Nutrition Leadership** * Develop and execute a nutrition strategy that supports the company’s long\-term vision and market positioning. * Provide strategic input into product innovation, portfolio planning, and health\-focused initiatives. * Collaborate with cross\-functional teams to embed nutrition into brand and business strategies. **Product** **Development \& Reformulation** * Define the nutritional profile and metrics of our products, ensuring alignment with our strategy and regulatory standards. * Support reformulation efforts to improve nutritional value while maintaining taste and quality. * Monitor scientific developments and translate them into strategic opportunities. **Consumer** **\& Stakeholder Engagement** * Partner with Marketing and Communications to develop credible, science\-based messaging. * Represent the company in external forums, including industry bodies, academic partnerships, and public health initiatives. **Insights** **\& Reporting** * Analyse nutrition\-related data and trends to inform strategic decisions. * Prepare reports and presentations for senior leadership and external stakeholders. **What can you expect from us?** This is a great opportunity to join a big team in a multicultural and modern environment. We foster innovation and team work, and we care for health and sustainability, which is at the center of our strategy. At GBfoods we don’t just accept our differences but we fully support and celebrate them. You will be able to grow and develop your skills and career in a consolidated company in the industry and also enjoy all our benefits! * Meals voucher * Breakfasts * Corporate Gym * 2 teleworking days/week * Flexible compensation And more! **Requirements**: * Degree in Nutrition, Dietetics, Food Science, or a related discipline (Master’s or PhD preferred). * Minimum 5 years’ experience in a nutrition or health\-related role within the food industry. High preference for branded food manufacturer experience. * Proven experience in strategic planning or working within a strategy\-focused function. * Strong understanding of food regulations, health claims, and consumer health trends. * High preference for having participated in a definition of a new nutritional strategy and metrics in the previous job experience. * International profile (across multiple EU markets) **What do we expect from you?** Our values define us and we expect you to show Authenticity, Proximity, Ownership and Joy to create true GBhood!

Plaça de l'Ajuntament, 4, 08901 L'Hospitalet de Llobregat, Barcelona, Spain

Homologation engineer - CAV647067887687691210

Homologation engineer - CAV

**Company Description** ***Shaping the Future of Automotive Engineering*** Applus\+ IDIADA is a global leader in automotive engineering, offering a dynamic and rewarding career opportunity for professionals passionate about shaping the future of mobility. As a TOP Employer certified company with over 3400 professionals in 24 countries, we provide a diverse and inclusive work environment that fosters innovation and growth with colleagues from over 57 nationalities contributing to a safer, more efficient, and sustainable vehicles. **Why join us?** Enjoy a highly flexible hybrid work model in a company that takes care of the employees’ wellbeing, offering work\-life balance benefits such as subsidized canteen, free language courses, transport and coaching services. Join a company that has a deep commitment to sustainability and push yourself to reach your full potential in a dynamic and challenging setting that values innovation and expertise. ***Come \& join us on the road to success.*** **Job Description** Our Homologation department is looking for an Engineer to join the team. **Role**: * Perform activities within the scope of projects of Homologation of ADAS systems, Automated Vehicle and related vehicle regulations * Manage projects of Cybersecurity and Software update certification **Main responsibilities**: * Participation in R\+D projects * Analysis of internal processes and improvement * Analysis of manufacturer's documentation * Prototype assessment, preparation, instrumentation and test, both at IDIADA HQ and in other locations worldwide * Analysis of test results * Homologation reports * Manage the whole approval process including multidisciplinary teams * Meetings with manufacturers and approval authorities **Qualifications** **Education**: * Degree in Industrial/mechanical/telecommunications/electronics/IT/aeronautical engineering. (MSc valued) * Other engineering degrees or master acceptable depending on competences and experience. **Experience**: * Experience in automotive engineering valuable. * Experience in quality systems valuable. * Experience in Project Management valuable. * Knowledge or experience in quality control, regulation or standards. * Knowledge or experience in measuring systems, procedures and equipments. * Knowledge in new automotive technologies related to General Safety Regulation 2: intelligent vehicle safety and dynamic systems **Languages**: * High level of English (other languages valued, French, Italian, German,...). **Additional Information** **What are the phases of the selection process?** Here's your roadmap: * 1st: Submit your application and complete our screening questions. * 2nd: Quick chat with HR or pre\-recorded interview to be completed online. * 3rd: Interview with the hiring team and complete English and attitudinal assessments. * 4th: Receive your offer and begin your onboarding journey. Let's start this adventure together! Applus IDIADA is committed to **equality,** **diversity** and **inclusion**. We don’t put limits on you, so don’t put limits on yourself either. There is a place for everyone.

7FMM+88 La Bisbal del Penedès, Spain

Machine Operator- Optical Sorting Machine Technician647330123008021211

Machine Operator- Optical Sorting Machine Technician

**Machine Operator – 1st and 2nd Shift** **CELO USA \- Trident Fasteners, Inc.** is the U.S. branch of CELO, a global leader in fastener manufacturing. We specialize in precision screws for industrial applications, including cold\-formed parts, licensed thread rolling screws for metals, and self\-tapping screws for plastics. Based in **Kentwood, Michigan**, we are seeking a highly motivated, detail\-oriented, and enthusiastic team player to join our production facility for an immediate opening. **Position: Machine Operator – 1ts and 2nd Shift (Sorting Department) Key Responsibilities.** Operate and maintain high\-precision sorting machines utilizing laser or camera\-based technology to accurately classify screws according to specifications. As a Machine Operator in our Sorting Department, you will be responsible for the efficient setup, operation, and basic maintenance of our specialized production sorting equipment. Your duties will include: * Setting up, operating, and monitoring production sorting machinery to ensure optimal performance and product quality. * Performing routine **quality control checks** using precision measuring tools to confirm product specifications and adherence to blueprints. * Conducting basic preventative maintenance and troubleshooting on equipment to minimize downtime. * Accurately documenting production data, quality checks, and maintenance activities into the computer system. * Operating a **forklift** as needed for material handling and logistics within the department. * Maintaining a clean, organized, and safe work environment. **Schedule \& Compensation** * **Schedule:** Full\-Time, 40 hours per week. * Monday \- Thursday (4x10 hour shifts). * **Pay:** $19\.00 \- $21\.00 per hour (Based on experience). **Qualifications Required** * High school diploma or equivalent. * Demonstrated ability to use **measuring tools** (e.g., calipers, micrometers). * Comfortable utilizing basic computer software for data entry and documentation. * Proven **detail\-orientation** and commitment to accuracy in a manufacturing environment. * Ability to thrive in a fast\-paced production setting. **Preferred** * Previous experience operating and setting up production machinery, especially sorting equipment. * Proficiency in reading and interpreting **blueprints** and technical specifications. * Current or previous certification/experience operating a forklift (or willingness to learn and be certified). * Bilingual proficiency (English/Spanish is a plus). **Job Type:** Full\-time **Benefits:** * 401(k) * 401(k) matching * Dental insurance * Health insurance * Health savings account * Life insurance * On\-the\-job training * Paid time off * Referral program * Tuition reimbursement * Vision insurance **Ability to Commute:** * Kentwood, MI 49512 (Required) **Ability to Relocate:** * Kentwood, MI 49512: Relocate before starting work (Required) **Work Location**: In person

Lloc Horts Torrent Canyelles, 102, 08211 Castellar del Vallès, Barcelona, Spain

Reliability Engineer647330123176991212

Reliability Engineer

Welcome to this recruitment process with Vueling! Applying is your first step to having the opportunity to join the **first Top Employer airline in Europe.** We hope the information you find here encourages you to apply so we can get to know you and stay connected. Let's start by getting to know us better! **At Vueling, we love things to happen.** We always do our best to go one step further and do it better. We invite our people to celebrate their unique strengths, work as a team to overcome challenges and achieve their goals for the greater good. Our team is made of great professionals. Great and passionate people who collaborate, support and complement each other's skills. **We are one of Europe's leading low\-cost airlines, with special relevance in the Spanish domestic market, as well as in France and Italy.** **Job Purpose** Ensure comprehensive monitoring and enhancement of fleet reliability through rigorous data analysis, preparation of Key Performance Indicators (KPIs), and regular reporting to Aeronautical Authorities, following strict regulatory guidelines, with the goal of optimizing fleet performance and maintaining compliance. **Main Accountabilities** * Ensure fleet operations meet or exceed industry reliability standards and regulatory compliance. * Provide a clear and quantifiable measure of fleet performance to guide operational improvements. * Compile comprehensive datasets to facilitate detailed reliability assessments. * Identify root causes of reliability issues and propose actionable solutions. * Ensure a transparent and accountable record of fleet reliability performance and improvement actions. * Maintain open communication with regulatory bodies and demonstrate ongoing commitment to reliability and safety. * Ensure KPIs remain relevant and effective in driving operational decisions and improvements. * Foster a multidisciplinary approach to enhancing fleet reliability, ensuring comprehensive solutions are developed and implemented. * Fulfill the mission of the job if it is in the employee´s hand. **Main Responsibilities \- Tasks** * Systematically review and assess the reliability performance of the fleet, ensuring compliance with regulatory standards. * Develop and maintain KPIs that accurately reflect the operational reliability of the fleet. * Collect relevant operational data from various sources for reliability analysis. * Conduct thorough analyses of gathered data to identify trends, patterns, and areas for improvement in fleet reliability. * Document findings from reliability analyses in detailed reports for internal and regulatory review. * Present bi\-monthly reliability reports to Aeronautical Authorities, showcasing compliance and improvements. * Continuously refine and update KPIs to reflect changing operational realities and improvement initiatives. * Work collaboratively with engineering, maintenance, safety, quality, and operational teams to implement reliability improvements. * Perform any other responsibility or function that is assigned inherent to the job. **Main Relationships** * Manufacturers: Collaborating on issues related to aircraft components and systems, seeking solutions, and implementing modifications or maintenance actions. * Civil Aviation Authority: Ensuring compliance with regulatory requirements and standards for fleet reliability, and participating in audits. * Maintenance Providers: Working closely with providers on the execution of maintenance strategies, modifications, and addressing specific aircraft issues. * Engineering Department: Collaborating on technical issues, maintenance strategies, and the implementation of corrective actions. * Operations Department: Interacting with flight operations to ensure aircraft reliability does not impact operational efficiency. * Safety and Quality Departments: Coordinating on matters related to the reliability program's influence on overall safety and compliance with quality standards. * Technical Services: Collaborating on the analysis of technical data, defect trends, and the development of solutions to enhance reliability. * Ground Operations: Occasionally engaging with ground operations for issues that may affect aircraft reliability and turnaround times. **Education** Degree in Aeronautical, Mechanical, or Industrial Engineering **Experience** A minimum of **3 years** of experience in the aviation sector, preferably within a Continuous Airworthiness Management Organization (CAMO) environment or with a supplier of aviation components. **Languages** English C1 **Location** Viladecans, Barcelona **Level** Individual Contributor 5 **We are the only Top Employer airline in Europe** -------------------------------------------------- For the second year running, **Vueling** is the only European airline and the only low\-cost airline in the world to obtain this certification. The Top Employers Institute programme certifies organisations based on the participation and results of their HR Best Practices Survey. This survey covers six HR domains consisting of 20 topics including People Strategy, Work Environment, Talent Acquisition, Learning, Diversity, Equity \& Inclusion, Wellbeing and more. **\#FlyToYourFullPotential** Every single person who works with us is unique. Join us is accepting the invite to fly to your full potential through self\-development and pursuing your professional passion. Our employee value proposition and benefits include staff travel, discounts, a flexible working model, and more! Want to learn more? Click here. **Our Culture** We thrive on **teamwork** and **collaboration**. Joining our team means being part of a cohesive unit that works together, shares knowledge, and supports each other. Our **positive working atmosphere** is unique and essential to our productivity and growth. You'll be surrounded by diverse and dynamic professionals. We are passionate about what we do: **Connecting People and Places!** Learn more about our Mission, Vision, \& Values. **Our Recruitment Process** Your experience as a candidate is critical for us. We firmly believe that understanding our process will alleviate anxiety and **ignite your passion** for this extraordinary experience! Please take a closer look at how our process works.

Carrer d'Antonio Machado, 2h, 08840 Viladecans, Barcelona, Spain

Industrial Painter647073729884191213

Industrial Painter

At **KISEKI**, we specialize in Applied Engineering, focusing on Projects, Installations, and Industrial Assembly—covering mechanical, electrical, regulation, and control systems—as well as Industrial Maintenance, including corrective, preventive, and predictive maintenance. We are seeking to hire an industrial painter with electromechanical knowledge who wishes to join our team with commitment and enthusiasm for professional growth. **RESPONSIBILITIES:** * Surface preparation * Application of coatings * Operation of equipment and tools * Quality control * Support in the industrial maintenance department: equipment inspection, fault diagnosis, and use of various electric and manual tools. **WE OFFER:** * Genuine opportunity for job stability * Salary to be discussed during the interview, based on qualifications and experience * Potential for career advancement * Proven experience in companies within the sector. * Minimum three years’ experience performing duties similar to those required for this vacancy. * Higher Vocational Training Certificate in Installation and Maintenance, Mechanics, or a related field.

Correcans Polígon Cal Saio, Avinguda de Josep Anselm Clavé, 122, 08820 El Prat de Llobregat, Barcelona, Spain

Launch Lead - Immunology646092114364191214

Launch Lead - Immunology

In the BioPharma Business Unit (BBU), we turn ideas into life changing medicines. Working here means thinking big and working together to make the impossible a reality. We’re passionate about the potential of science to address the unmet needs of patients around the world. We commit to those areas where we believe we can really change the course of medicine and bring big new insights to life. In our ever\-changing environment the importance of finding a blend between innovation and new ways of working while keeping focus on the core principles for impactful interactions with our external customers is more important than ever. In short, launch success is at the center of for the long\-term success of patients, for the societies overall and for the BBU. The Global Business Excellence function forms part of Global Insights \& Business Excellence and is the Global BBU function that; * Develop global pre\-launch frameworks, set launch guidelines, and develop and track pre/post launch KPIs, ultimately securing that that the BBU maximise the potential of each asset to the benefit of patients and for AstraZeneca. * Outlines the commercial capabilities need for future success, secure that these capabilities are developed across the BBU markets/functions, and that owns the assessment of the quality of the execution of these capabilities. The vision for Global Business Excellence is to support the BBU 2030 Ambition with a relentless focus on securing pre\-launch excellence, future proofing BBU performance with elevated world class capabilities, and transforming care pathways . As global launch lead, the overall responsibility is twofold, securing launch readiness and drive launch uptake. In the pre\-launch phase, the launch lead is responsible for; * Embed the BBU launch framework and outline brand aligned launch guidance. * Drive use of LaunchPAL, track global and local progress across key areas. * Set and track pre\-launch KPIs and conduct Launch Readiness Reviews with local affiliates. * Outline brand capability plans aligned to brands with global brand VP. * Set resources guidance and conduct resource assessments based on Mid\-Term Planning submission. During the post\-launch phase, the launch lead is responsible for; * Post\-Launch reviews with key markets to secure that needed actions are taken to further catalyse launch uptake. * Conduct triangulation analysis between performance metrics and diagnostic metrics leveraging data from SFE reports, AICoach, ATU, SAS \& iCAST, to track launch progress, drive needed actions and share best practice. * Review and launch brand capability plans in alignment with global brand VP. * Lead above market diagnostic reporting securing that needed adjustments to global strategy take place. This role reports into the Head of Global Business Excellence supports BBU Global Brand Teams, Regions, and Marketing Companies (MCs), with priority on Top8 MCs. The Global launch lead team overall consists of a team of 7 FTEs. **Essential Skills \& Experience:** * Significant experience in biopharma industry, with a strong preference for experience from BUD / marketing manager roles. * Strong TA expertise with a track record of successful launches, Immunology experience is plus * Proven ability to drive performance and track record of successful P\&L ownership. * Strong influencing skills and collaborator management, including at an Executive Level * Experience in outlining and pulling through brand strategy * Understanding of and adaptable to working variances of different countries and different cultures * Demonstrated ability to manage and lead teams in a complex matrix organization. *The annual base pay for this position ranges from $229,303 to $343,954\. Hourly and salaried non\-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job\-related knowledge, skills, and experience. In addition, our positions offer a short\-term incentive bonus opportunity; eligibility to participate in our equity\-based long\-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program \[401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at\-will position” and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.*

Carrer de Joan Güell, 114, Les Corts, 08028 Barcelona, Spain

€ 229,303-343,954/year

Cook646952375018271215

**Additional Information** **Job Number**25196947 **Job Category**Food and Beverage \& Culinary **Location**Le Meridien Barcelona, La Rambla 111, Barcelona, Barcelona, Spain, 8001 **Schedule**Full Time **Located Remotely?**N **Position Type** Non\-Management **POSITION SUMMARY** Prepare ingredients for cooking, including portioning, chopping, and storing food. Wash and peel fresh fruits and vegetables. Weigh, measure, and mix ingredients. Prepare and cook food according to recipes, quality standards, presentation standards, and food preparation checklist. Prepare cold foods. Operate ovens, stoves, grills, microwaves, and fryers. Test foods to determine if they have been cooked sufficiently. Monitor food quality while preparing food. Set\-up and break down work station. Serve food in proper portions onto proper receptacles. Wash and disinfect kitchen area, tables, tools, knives, and equipment. Check and ensure the correctness of the temperature of appliances and food. Follow all company and safety and security policies and procedures; report maintenance needs, accidents, injuries, and unsafe work conditions to manager; complete safety training and certifications. Ensure uniform and personal appearance are clean and professional; maintain confidentiality of proprietary information; protect company assets. Speak with others using clear and professional language. Develop and maintain positive working relationships with others; support team to reach common goals; listen and respond appropriately to the concerns of other employees. Ensure adherence to quality expectations and standards. Stand, sit, or walk for an extended period of time or for an entire work shift. Reach overhead and below the knees, including bending, twisting, pulling, and stooping. Move, lift, carry, push, pull, and place objects weighing less than or equal to 25 pounds without assistance. Perform other reasonable job duties as requested by Supervisors. PREFERRED QUALIFICATION Education: High school diploma or G.E.D. equivalent. Related Work Experience: At least 1 year of related work experience. Supervisory Experience: No supervisory experience. License or Certification: None *At Marriott International, we are dedicated to being an equal opportunity employer, welcoming all and providing access to opportunity. We actively foster an environment where the unique backgrounds of our associates are valued and celebrated. Our greatest strength lies in the rich blend of culture, talent, and experiences of our associates. We are committed to non\-discrimination on any protected basis, including disability, veteran status, or other basis protected by applicable law.* At Le Méridien, we are inspired by the era of glamorous travel, celebrating each culture through the distinctly European spirit of savouring the good life. Our guests are curious and creative, cosmopolitan culture seekers that appreciate moments of connection and slowing down to savour the destination. We provide authentic, chic and memorable service along with experiences that inspire guests to savour the good life. We’re looking for curious and creative people to join our team. If you appreciate connecting with like\-minded guests and have a deep desire to create memorable experiences, we invite you to explore career opportunities with Le Méridien. In joining Le Méridien, you join a portfolio of brands with Marriott International. **Be** where you can do your best work, **begin** your purpose, **belong** to an amazing global team, and **become** the best version of you.

Ctra. Arrabassada - Camí de Sant Medir, 08196, Barcelona, Spain

Electromechanical Technician – Industrial Installations646097987895061216

Electromechanical Technician – Industrial Installations

**Description:** ---------------- **Grupo Savia** is actively seeking an **Electromechanical Technician** to join our Installation Team for industrial assembly and disassembly projects. Work is carried out on-site across the entire **national and international territory** (occasionally), and it is essential to have **availability for travel and overnight stays**, as well as **personal transportation**. Your responsibilities will include: * Assembling electrical and mechanical equipment and low-voltage power installations, including wiring, installing conduits (trays, pipes, etc.), and connecting equipment. * Conducting relevant safety and functional tests. * Assembling, inspecting, and maintaining electronic equipment, regulation and control devices for installations, and AC or DC electric machinery in optimal condition. * Assembling mechanical assemblies using machinery, tools, or manual methods based on assembly drawings. * Verifying functionality, precision, and quality of parts, materials, and assemblies prior to installation. * Adjusting all components for commissioning. * Adjusting and verifying mechanical system parameters (lubrication, bolting and securing components, checking dimensions, etc.). * Installing pneumatic systems for various components. * Always complying with established safety, hygiene, quality, and environmental regulations, and ensuring adherence thereto. **Requirements:** --------------- * Vocational Training Certificate (CFGM or CFGS) in Electromechanics / Equivalent Professional Certification. * Minimum 4 years’ experience in mechanical, pneumatic, and electrical machinery assembly. * Knowledge of electricity and mechanics. * Minimum 4 years’ experience in industrial installations. * Knowledge of low-voltage electrical power equipment and installations. * Ability to read and interpret technical information contained in project documents, technical reports, schematics, and diagrams. * Ability to consult catalogs, service and user manuals, UNE standards, low-voltage regulations, safety regulations, municipal ordinances, and building codes.

Carrer Tirso de Molina, 34, 08940 Cornellà de Llobregat, Barcelona, Spain

CNC TURNER (FIRST-CLASS) IN CASTELLBISBAL646097988199711217

CNC TURNER (FIRST-CLASS) IN CASTELLBISBAL

SIMA, a company specializing in maintenance services for industrial plants, infrastructure, and buildings, is seeking to hire a CNC Turner for its Barcelona office located in Castellbisbal. The selected candidate, reporting to the Team Leader, will be responsible for: machining large-size parts; operating CNC lathes, with particular emphasis placed on experience with Fagor controls; handling parts using an overhead crane; ensuring machining quality and compliance with established standards. Requirements: Higher Vocational Training Degree in Machining or equivalent; minimum of 2 years’ experience in a similar position; experience handling large parts using an overhead crane. Desirable: knowledge and experience with Fagor CNC lathes. Offer: Opportunity to join an established company specialized in industrial maintenance management; integration into a professional team with strong industry reputation; working schedule: rotating shift from Monday to Sunday. The selected candidate, reporting to the Team Leader, will be responsible for: machining large-size parts; operating CNC lathes, with particular emphasis placed on experience with Fagor controls; handling parts using an overhead crane; ensuring machining quality and compliance with established standards. Experience: 2 years. Minimum two years’ experience in a position similar to the one offered. * Permanent employment contract * Intensive work schedule * Other relevant information: Gross annual salary between €28,000 and €31,000

Plaça els Bellots, 772, 08227 Barcelona, Spain

€ 28,000-31,000/year

Quality Manager Contamination Control PPC Division646092111904021218

Quality Manager Contamination Control PPC Division

### **Role Overview:** The Quality Manager for Ecolabs ppc division contamination control range will play a senior leadership role in auditing and ensuring that Ecolab’s quality system requirements are met across all PPC production sites globally. This position is responsible for timely and satisfactory resolution of complaints, establishing quality control guidelines and testing procedures, and ensuring that raw materials and finished products comply with engineering and product specifications. Additionally this position will ensure our critical contamination control range of products sold to pharmaceutical customers meets specifications and customer expectations throughout shelf life. ### **Key Responsibilities:** * Ensure compliance with Ecolab quality system requirements across all PPC production sites. * Ensure new product introductions are handled appropriately with strong validation activity to ensure RFT and no issues in market. * Oversee and manage the resolution of customer complaints promptly and effectively. * Develop and implement quality control guidelines and testing procedures. * Verify that raw materials and finished products meet engineering and product specifications. * Make decisions regarding product disposition based on quality standards. * Authorise requisition of supplies and services critical to the quality function ### **Qualifications:** * Bachelor’s degree in **Chemistry**, **Engineering**, **Food Science**, or a related field with a strong chemistry component. * **10\+ years** of experience managing quality systems, including at least **3 years** in a related industry. * Strong knowledge of quality standards, including pharma GMP and regulatory requirements. * Proven leadership skills and ability to operate independently. **Our Commitment to a Culture of Inclusion \& Belonging** Ecolab is committed to fair and equal treatment of associates and applicants and furthering the principles of Equal Opportunity to Employment. We will recruit, hire, promote, transfer and provide opportunities for advancement based on individual qualifications and job performance in all matters affecting employment, compensation, benefits, working conditions, and opportunities for advancement. Ecolab will not discriminate against any associate or applicant for employment because of race, religion, color, creed, national origin,citizenship status, sex, sexual orientation, gender identity and expressions, genetic information, marital status, age, or disability.

Carrer de Montilla, 7, 08970 Sant Joan Despí, Barcelona, Spain

Mechanical Engineer645988020860171219

Mechanical Engineer

Who We Are VEGA Chargers is a company specialising in the design and manufacturing of fast chargers (DC) for electric vehicles. At VEGA Chargers, we work tirelessly to create a more sustainable present and future in terms of mobility. We analyse our customers’ needs to deliver flexible, efficient, and scalable charging solutions. From concept to design, through manufacturing and distribution — every step is driven by innovation and collaboration. What We Are Looking For We are seeking a Mechanical Design Engineer to join our Product Development team. This role will focus on the design, development, and optimisation of mechanical components and structures that integrate seamlessly with our electronic and electrical systems. We’re looking for a creative and detail\-oriented professional passionate about mechanical design, tooling, and cost\-efficient solutions for high\-performance EV charging products. Your Responsibilities Will Include Product \& Mechanical Design * Participate in the entire product design process, ensuring mechanical components align with electronic and electrical requirements. * Design metal structures supporting electronic components and external enclosures. * Develop 3D models and detailed product drawings using CREO Parametric. Tooling \& Production Support * Design auxiliary tools and jigs to improve manufacturing efficiency and assembly precision. * Support production teams by ensuring tooling solutions are functional, reliable, and ergonomic. Process Optimization \& Cost Management * Analyse product performance and implement design improvements based on testing and feedback. * Optimize mechanical solutions to reduce costs while maintaining quality and robustness. Cross\-Functional Collaboration * Work closely with Electrical, Hardware, Software, and Production teams to ensure smooth integration of all system components. * Contribute to continuous improvement of design methodologies and documentation standards. Requirements * Degree in Industrial Design Engineering or Mechanical Engineering. * Proven experience in 3D modeling (CREO Elements / Parametric, SolidWorks, or Catia). * Knowledge of sheet metal fabrication, mechanical integration, and production tooling design. * Understanding of mechanical\-electronic interfaces and manufacturing processes. * Strong attention to detail and problem\-solving mindset. * Excellent communication and teamwork abilities. Nice to Have * Experience in the electric vehicle or electronics manufacturing industry. Benefits * Coffee \& Snacks 22 days of holidays 1 day working from home (after the first month) Be part of an innovative team where your opinion truly matters. Work on products that shape the future of sustainable mobility. Selection Process **1\. Initial call with People:** get to know VEGA Chargers and share your story. 2\. Interview with Lluís (CBO) \& Israel (CTO). 3\. Job Offer

Carrer del Mestre Pla, 9, 08211 Castellar del Vallès, Barcelona, Spain

Immunology Scientist645985739973131220

Immunology Scientist

We are looking for a Scientist for our Immunology department. Under the supervision of the Department Manager, the Scientist will be responsible for the following duties: * Develop and validate immunological and cellular tests according to the guidelines of regulatory agencies (EMA, FDA, ICH). * Apply the developed and validated tests to the analysis of samples from preclinical and clinical studies, as well as the quality control analysis of biological products using cellular assays. * Direct and / or execute studies under GLP and GMP standards. * Prepare protocols and final reports of the studies. * Manage the assigned projects keeping the deadlines and establishing a direct communication with the client. * Lead and/or coordinate the work of the technical staff in charge. The ideal candidate should have: * Degree in Health Sciences (Biology, Biotechnology, Biochemistry, Pharmacy, or similar). * Extensive experience in immunoassays (ELISA, ECLA, etc.) and especially in cell based assays. * Experience in working in GXP environments. * Knowledge of applied statistics. * English level First Cetificate. **If you join us, you will become part of an agile and growing company with a strong scientific culture.** Here's what you can expect: * A collaborative, empowering environment focused on continuous learning and professional growth. * Flexible Hours and intensive Fridays. * A Flexible employee benefits platform. * 23 vacation days per year \+ 24th and 31st of December as holidays. * A Fully stocked kitchen (Coffee, fruits, snacks, and beverages). * An inspiring workplace surrounded by nature\- our headquarters located at the foot of Collserola Natural Park (Barcelona) with a Rooftop terrace an beautiful views. Kymos considers diversity and inclusion as key development priorities, with one of our main goals being to promote a culture that embraces differences and celebrates unique talents. For this reason, we are committed to equal opportunities for all people, regardless of gender, nationality, sexual orientation, gender identity, age, religion or any other personal characteristic.

Carrer de Lluís Companys, 2, 08290 Cerdanyola del Vallès, Barcelona, Spain

Postdoctoral Researcher (Clinical biochemistry, drug delivery & therapy)645508746542101221

Postdoctoral Researcher (Clinical biochemistry, drug delivery & therapy)

VHIR offers a vacant position for a Postdoctoral researcher at the Clinical Biochemistry, Drug Delivery \& Therapy group. The candidate will be hired within the European project CancerScan project to assist in its development. Our group is experienced in developing and testing in pre\-clinical models a spectrum of nanomedicines. Within the CancerScan project pancreatic cancer\-derived spheroids will be produced and employed to elucidate the influence of cancer communication mediated by extracellular vesicles (EVs) in response to therapy. The candidate’s main tasks will be to assist in the synthesis of spheroids as well as the further analysis of subsets of secreted EVs, including their monitoring, isolation and characterisation under distinct treatment regimens. In addition, the candidate will also work with the FVPR/U20 service platform of the group. FVPR/U20 is dedicated to performing customised production and functional assays for the preclinical development of novel diagnostic or therapeutic compounds based on nanotechnology. FVPR/U20 is part of ICTS\-Nanbiosis and operates in an ISO9001:2015 certified environment. The candidate will also perform tasks for national and international projects of the CB\-DDT group and contribute to the laboratory management. https://vhir.vallhebron.com/en/research/clinical\-biochemistry\-drug\-delivery\-therapy https://vhir.vallhebron.com/en/research\-support/functional\-validation\-and\-preclinical\-research https://www.nanbiosis.es/portfolio/u20\-in\-vivo\-experimental\-platform/ **Education and qualifications:** ###### **Required:** * PhD in Biological Sciences (Biology, Biotechnology, Biomedicine) Fluency in English (professional level) * ###### **Desired:** * Fluency in Catalan ##### **Experience and knowledge:** ###### **Required:** * Extensive training in cell culture, molecular biology and bioproduction processes * Previous experience working with Extracellular Vesicles and other nanoparticles * Analytical, organizational and time management skills * Ability to work independently Good computer skills, including MS Office, GraphPad, FlowJo, ImageJ, R. * ###### **Desired:** * Knowledge in bioinformatics * Experience in Quality Management Systems * We are looking for someone with a hands\-on attitude, who is flexible and adaptable. Additionally, the following personal skills are desirable: + Teamwork + Proactivity + Well\-organized and responsible person at work ##### **Main responsibilities and duties:** * Cell culture: basic maintenance (subculturing, freezing and storing), functional assays (cell proliferation, apoptosis, etc) of a variety of cultures available in the laboratory. * Complete molecular biology characterisation of cell cultures after treatment with different chemotherapeutic agents. * Characterisation and handling of different types of nanomaterials, especially extracellular vesicles. * Generation of scientific reports and presentations. **Labour conditions:** * Full\-time position: 40h/week * Starting date: 01/01/2026 * Gross annual salary: 24\.785,40 euros (Remuneration will depend on experience and skills. Salary ranges are consistent with our Collective Agreement pay scale) * Contract: *Technical and scientific activities contract linked to the project activities* ##### **What can we offer?** * Incorporation to Vall d’Hebron Research Institute (VHIR), a public sector institution that promotes and develops the biomedical research, innovation and teaching at Vall d'Hebron University Hospital (HUVH), the biggest hospital of Barcelona and the largest of Catalan Institute of Health (ICS). * A scientific environment of excellence, highly dynamic, where high\-end biomedical projects are continuously developed. * Continuous learning and a wide range of responsibilities within a stimulating work environment. * Individual training opportunities. * Flexible working hours. * 23 days of holidays \+ 9 personal days. * Flexible Remuneration Program (including dining checks, health insurance, transportation and more) * Corporate Benefits: platform through which you can obtain significant discounts on travel, culture, technology, gastronomy, sports... among many others. * Healthy Offering: choose from a variety of wellbeing focused activities to be the healthiest you. * International Mobility Support (Welcome Services): We aim to make your arrival in Barcelona smooth and pleasant by providing city information, guidance on required procedures, access to the International Welcome Desk, family recommendations, and support in finding accommodation **Deadline to apply: 11\-12\-2025** **How We Hire:** ***Pre\-selection:*** *Candidates are shortlisted based on their skills, qualifications, and relevant experience as outlined in their CVs.* ***Interviews:*** *Meetings may be held with Talent Acquisition and/or the hiring manager.* ***Practical assessment:*** *Depending on the role, candidates may complete a case study, technical task, presentation, or written exercise, on\-site or remotely.* ***Checks:*** *Education, references, and other job\-related verifications may be carried out.* ***Job offer:*** *The selected candidate receives a formal job offer upon successful completion of the process.* *VHIR embraces Equality and Diversity. As reflected in our values we work toward ensuring inclusion and equal opportunity in recruitment, hiring, training, and management for all staff within the organization, regardless of gender, civil status, family status, sexual orientation, gender identity and expression, religion, age, functional diversity or ethnicity.*

Carrer Sagàs, 11, Horta-Guinardó, 08035 Barcelona, Spain

€ 24,785/year

Flow Cytometry Expert (Ref. CF/25/08)645508744423711222

Flow Cytometry Expert (Ref. CF/25/08)

Created in 2005 by the Generalitat de Catalunya (Government of Catalonia) and the University of Barcelona, IRB Barcelona is a Severo Ochoa Centre of Excellence—a seal that was awarded in 2011\. The institute is devoted to conducting research of excellence in biomedicine and to transferring results to clinical practice, thus improving people’s quality of life, while simultaneously promoting the training of outstanding researchers, technology transfer, and public communication of science. Its 29 laboratories and seven core facilities address basic questions in biology and are orientated to diseases such as cancer, metastasis, Alzheimer’s, diabetes, and rare conditions. IRB Barcelona is an international centre that hosts 500 members and 45 nationalities. It is located in the Barcelona Science Park. IRB Barcelona forms part of the Barcelona Institute of Science and Technology (BIST) and the “Xarxa de Centres de Recerca de Catalunya” (CERCA). **Your role \& our team** IRB Barcelona seeks to recruit a dedicated **Flow Cytometry Expert** to support the day\-to\-day operations of its newly established Flow Cytometry Service. Currently equipped with two instruments (BD FACSymphony S6 and BD FACSymphony A5 SE), the service is designed to provide IRB researchers with high\-quality training, technical assistance, and scientific guidance with the aim to empower scientific discovery through accessible, expert\-driven cytometry support. We are looking for a highly motivated individual who is eager to learn and grow within the role, and who brings the personal competences needed to thrive in a service\-based environment, including strong interpersonal skills and a high degree of initiative. **Key responsibilities:** * Daily operation of the cell sorter and provide user support on the analyzer platform. * Provide technical support and expert advice on flow cytometry, experimental design, panel design, protocol optimization and execution. * Provide support in flow cytometry software and data analysis. * Provide comprehensive training in flow cytometry fundamentals, data analysis and the use of flow cytometry analyzers. * Manage and perform preventive and corrective maintenance of cytometers and cell sorters under their responsibility. * Perform quality control and quality assurance procedures. * Monitor equipment usage and prepare periodic reports to evaluate resource optimization and identify new needs. * Management of reports and data backups. * General lab organization and administrative tasks. **You have:** * A degree in immunology, biology, chemistry or related fields. * Familiarity and hands\-on experience (\>2 years) with flow cytometry equipment (including cell sorting), flow cytometry procedures, flow cytometric data analysis, and technical troubleshooting. * Good working knowledge of common flow cytometry software (FACSDiva, FlowJo). * Experience in general lab management (e.g. purchasing and stock controls, working with field service engineers, routine calibration and QC, waste management). * Proficiency in Spanish and English. * Capacity to work both independently and as part of a team. * Excellent interpersonal and communication skills. * Troubleshooting capacity and attention to detail. * Custom oriented. **You might also have** * Previous experience in a flow cytometry platform. * Experience in multicolor panel design. * Experience in training users in flow cytometry applications and use of instrumentation. * Prior hands\-on experience in operating and troubleshooting a BD FACSymphony S6 and/or BD FACSymphony A5 SE. **What we offer:** **To be a part a part of something meaningful**: We are a biomedical research centre that tirelessly works to achieve a society free of diseases. Our mission is to carry out research of excellence to cure cancer and other diseases linked to ageing. **Good Working conditions:** Permanent contract. Employed in compliance with Spanish legislation and regulations under a full\-time contract. Employees receive the benefits of the Spanish Social Security system covering sickness, maternity/paternity leave and injuries at work. **Competitive salary:** commensurate with experience and qualifications. **International Environment:** we are home to nearly 500 researchers, technical and support staff from 45 countries. **To be a member of our State\-of\-the\-Art Core Facilities:** Scientists at IRB Barcelona thrive with unparalleled support from our extensive Core Facilities, equipped with the latest technologies and scientific services. These essential resources drive our research excellence, delivering cutting\-edge innovations rapidly to our team. **Continuous Training:** Transversal and general training is offered to our community (examples include research seminars, conferences, training in time management, scientific integrity, gender equality, health and safety, languages courses and emotional wellbeing). **Relocation \& Visa Assistance:** Trained staff provides support on visa paperwork, administrative requirements, and practical information on living and working in Barcelona, etc. **Social Life:** We like to have fun. We promote several activities, like a Football League, an annual skiing trip, a Mountaineering Club, a Running Club and "Cool\-off sessions", where members meet informally for drinks, snacks and scientific discussions. **Fairness:** Our recruitment is open, transparent and merit\-based, and all applicants compete on the same terms. We are an Equal Opportunity Employer and all qualified applicants are considered for employment without regard to race, colour, religion, age, sex, sexual orientation, gender identity, nationality, ethnic origin or disability. **HOW TO APPLY \& SELECTION PROCESS:** * **Deadline for applications**: 26/12/2025 (If no suitable candidate is found, the deadline will be extended) * **Number of positions available**: 1 * **Selection process:** + **Pre\-selection**: Will be based on CV, motivation letter \& experience, + **Interviews**: Short\-listed candidates will be interviewed. + **Job offer**: Will be sent to the successful candidate after the interview. *Note: The strengths and weaknesses of the applications will be provided upon request.*

Carrer de Joan Güell, 114, Les Corts, 08028 Barcelona, Spain

SMT Engineering Manager645332490644511223

SMT Engineering Manager

For our multinational automotive company based in the Electronics plant in Valls (Tarragona), we are looking for a highly qualified manager able to work in a very demanding environment. As an SMT Engineering Manager reporting to the Industrial Engineering Manager, you will be responsible for managing the industrialization of SMT products, ensuring customer requirements, quality, capacity, efficiency and continuous improvement of SMT manufacturing processes. **Responsibilities:** * Lead, manage, supervise and develop the SMT Engineering team. * Industrialize and set up production lines for new launches, ensure timing, quality, efficiency and set requirements. Manage customer needs and requests to obtain customer R\&R approval. * Provide capacity to increase volume, gain customer acceptance for each series of customer processes. * Implement efficiency improvements in manufacturing processes to enable high equipment saturation. * Provide tools and processes that will enable the proper implementation of changes in production. * Maintain the level of technical knowledge, ensure technological development on processes and production equipment. * Prepare and define investments, manage the reuse of equipment, by preparing technical and cost improvement studies. * Ensuring the traceability of processes according to customer requirements. * Production support in process optimization and troubleshooting support. **Requirements:** * Bachelor's degree in Industrial Engineering (Master's degree will be a plus). * High level of English, both spoken and written. * Proactive personality, showing initiative and efficiency. * Strong leadership and communication skills. * Experience in the automotive industry environment. * Knowledge/understanding of electronics manufacturing (SMT / automation / etc…).

Carrer Sant Sebastià, 20, 43800 Valls, Tarragona, Spain

Process Engineer Trainee645332489217311224

Process Engineer Trainee

Who We Are VEGA Chargers is a company specialising in the design and manufacturing of fast chargers (DC) for electric vehicles. At VEGA Chargers, we work tirelessly to create a more sustainable present and future in terms of mobility. To achieve this, we analyse our customers' needs and provide flexible and scalable charging solutions for electric vehicles. Our process starts from conceptualisation and design, leading to manufacturing and distribution. What We Are Looking For We are looking for an Engineering student eager to grow within the Process Engineering field. Someone proactive, curious, and motivated to learn how production processes are designed, industrialised, and optimised in a high\-tech environment. Your Responsibilities Will Include Process Support \& Development * Support the design and definition of production processes, including tooling, equipment needs, and manufacturing flows. * Assist in preparing layouts, production cycles, and technical documentation. * Participate in evaluating design changes and their impact on manufacturability and cost. Project Assistance * Help with planning and tracking industrialisation activities. * Support root\-cause analysis and corrective actions when deviations occur. * Assist during production ramp\-up and process validation. Quality \& Cost Optimization * Contribute to Process FMEA activities and continuous improvement initiatives. * Help identify efficient and quality\-compliant production solutions. Documentation \& Reporting * Maintain updated process documentation, reports, and records. * Collaborate closely with Production, Quality, R\\\&D, and Supplier Management teams. Requirements * Ongoing studies in Industrial, Mechanical, Electrical, Electronic Engineering, or similar. * Basic knowledge of 3D design and CAD tools. * Interest in process control methodologies and continuous improvement. * Strong analytical mindset, attention to detail, and willingness to learn. * Good level of English. Nice to Have * Experience with PLM tools. * Familiarity with manufacturing or industrial environments. Benefits * Coffee \& Snacks * Opportunity to contribute to technology shaping the future of e\-mobility. * Guidance and mentoring from the Operations team. Selection Process 1\. Introductory call with People. 2\. Meeting with the Operations team. 3\. Job offer.

Carrer del Mestre Pla, 9, 08211 Castellar del Vallès, Barcelona, Spain

Project Management Senior Specialist645234092989451225

Project Management Senior Specialist

**Job Title** Project Management Senior Specialist**Summary** In this role, you will contribute to the successful onboarding of ACRS customers by establishing and maintaining project governance frameworks, managing project documentation, and tracking budgets, milestones, and progress. The APS Enterprise Program Services – ACRS Implementation department is part of the rapidly growing Hospitality division within Amadeus. Our mission is to onboard customers onto ACRS, ensuring smooth transitions, consistent quality, and scalable execution across all delivery programs. You will help develop integrated project plans and facilitate coordination between Test, Deployment, Implementation streams, R\&D, Product, Partners and customer teams to ensure clear alignment and efficient execution. As your experience and domain knowledge grows, you will have the opportunity to expand your expertise into test management, deployment, or even implementation, to support ACRS onboarding of mid\-market customers. **Main responsibilities:** * Demonstrate knowledge within project and program delivery. Serve as a reference point for colleagues and supports less experienced team members when needed. * Anticipate dependencies, risks, and impacts in complex delivery environments. Contribute to cross\-functional initiatives and drives improvements in processes and practices. * Operate independently with guidance in the most complex scenarios and be accountable for delivering on commitments. * Establish and maintain project governance standards, processes, and tools that support consistent ACRS implementations. * Manage project documentation, reporting systems, financial tracking, risk logs, and change controls to ensure transparency and control. * Consolidate progress updates and performance data to support clear communication and informed decision\-making by stakeholders. * Facilitate project meetings and alignment across Test Management, Deployment, Implementation, R\&D, Product, Partners and customer teams. * Oversee SharePoint and other collaboration platforms to ensure effective information sharing and document management. * Develop training materials and provide guidance to support the adoption of project management practices and tools. * Proactively identify and address risks, issues, and interdependencies to keep projects on track. * Participate in communities of practice to share knowledge, contribute to continuous improvement, and build capability across the team. **About the ideal candidate:** * 3\+ years of professional experience in project management, PMO, or related operational roles. * Exposure to complex program or implementation environments, ideally within hospitality * Solid understanding of project management principles; PMP, ACP, or equivalent certification is a plus. * Exposure to measurement, analysis, and process improvement approaches. * Previous experience in implementation, combined with an interest in expanding into project management while maintaining a strong focus on understanding both functional and technical aspects, is highly desirable. * Highly organized, autonomous, and proactive in managing multiple priorities. * Strong analytical and conceptual thinking. * Excellent communication, interpersonal, and presentation skills. * Experience with Microsoft Ecosystem Tools (Excel, SharePoint, Power BI) **What we can offer you:** * A complete rewards offer \- Amadeus provides attractive remuneration packages, covering all essential components of a competitive reward offer, including bonus, equity, pension plan, travel, life and healthcare insurance, as well as lunch and transport allowance and other benefits. * A truly global DNA \- Everything at Amadeus is global, from our people to our business, which translates into our footprint, processes, and culture. * Great opportunities to learn \- Learning happens all the time and in many ways at Amadeus, through on\-the\-job training, formal learning activities, and day\-to\-day interactions with colleagues. * A caring environment \- Amadeus fosters a caring environment, nurturing both a fulfilling career and personal and family life. We care about our employees and strive to provide a supportive work environment. * A flexible working model \- We want our employees to do their best work, wherever and however it works best for them. * A diverse and inclusive community \- We are committed to leveraging our uniquely diverse population to drive innovation, creativity, and collaboration across our organization. * A Reliable Company \- Trust and reliability are fundamental values that drive our actions and shape long\-lasting relationships with our customers, partners, and employees. * A critical mission and purpose \- At Amadeus, you will be powering the future of travel and pursuing a critical mission and extraordinary purpose. \#LI\-EMEA **Diversity \& Inclusion** Amadeus aspires to be a leader in Diversity, Equity and Inclusion in the tech industry, enabling every employee to reach their full potential by fostering a culture of belonging and fair treatment, attracting the best talent from all backgrounds, and as a role model for an inclusive employee experience. Amadeus is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to gender, race, ethnicity, sexual orientation, age, beliefs, disability or any other characteristics protected by law.

Carrer de la Granada del Penedès, 4, Sarrià-Sant Gervasi, 08006 Barcelona, Spain

Engineer PMQ - 12month contract645233464431371226

Engineer PMQ - 12month contract

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position As an Engineer PMQ you will be dealing with complaints concerning Digital Solutions quality and product performance of Hospital/Laboratory Information Systems (HIS/LIS), medical data networks, middleware solutions. data communication, apps algorithms. As a member of the Digital Solutions Chapter, you will be working in a very transversal Software environment having the opportunity to work with cutting edge technologies and different programming languages for on\-premise and cloud\-based software. You need to be able to read and understand source code in order to find out the root cause/causal factor of a SW malfunction/SW issue, and also be able to learn about Software requirements, fixing bugs process (even if you will not fix them) and general code maintenance, all of it in an Agile environment where you could contribute with your own ideas and proposals in a team continuously improving **Your main responsabilities:** * You will be accountable for the timely handling of individual cases (Inquiry, Complaint, Potential Reportable and Safety issues) according to ISO Quality System requirements and regulations, and needs of the Country Organizations including creation, acceptance, classification, investigation, complete documentation, on\-site trouble\-shooting and resolution of cases. * Resolving cases in the assigned area, potentially requiring consultation with more senior team members on technical or process\-related aspects. * Assuming responsibility to ensure, by collaborating and interfacing with the BA and global and/or local functions, appropriate measures from cases are derived, including, but not limited to workarounds, in a timely manner. * Providing audit and inspection support as requested and contributing to the creation of regular reports to document on\-market product quality and performance, to escalate critical issues to the responsible Life Cycle Teams and to define pro\-active measures. * Supporting regular review of quality of case handling and analyze feedback on customer satisfaction to permanently optimize processes to increase quality and efficiency standards with a focus on customer, compliance and continuous improvement. **Who you are:** * You own a Graduate Degree from a University for Information Technology (IT) or Biomedical Engineering or from a Professional Education and Training College (Higher Technical School) or equivalent professional experience or you successfully passed a vocational training in Information Technology or Biomedical Engineering * You have more than 2 years of work experience in the area of information technology in either 1st or 2nd level support or R\&D related functions * You have strong communication skills in English (written and spoken) * You are able to read and understand source code in a programming language \& you have a passion for clean and structured code and solid future\-proof architectures having in mind testing strategies. * You are able to debug source code of different programming languages to understand the root cause of reported issues. Would be a plus: Knowledge of other database engine \& Knowledge of IVD regulatory requirements and quality practices, especially in the area of complaint management (e.g., 21 CFR 820\.198, ISO 10002, ISO 9001, ISO 13485\) At Roche, we are passionate about transforming patients’ lives, and we are bold in both decision and action \- we believe that good business means a better world. That is why we come to work every single day. We commit ourselves to scientific rigor, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow. Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life\-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. **Roche is an Equal Opportunity Employer.**

Carr. de Bellaterra, 17, 08205 Sabadell, Barcelona, Spain

Quality Manager645233465038101227

Quality Manager

An industrial company, leader in its sector and based in the Baix Llobregat area, is looking for a **Global Quality Manager** to lead its quality strategy across international operations. The role will ensure the highest standards of product excellence, drive continuous improvement, and reinforce a customer\-centric approach throughout the organization. **Main Responsibilities** * Define and implement a global quality strategy aligned with business goals and customer expectations. * Oversee the development, implementation, and maintenance of Quality Management Systems (ISO 9001, IATF 16949, etc.) across regions. * Lead initiatives to enhance product quality, reduce waste, and optimize processes through Lean and Six Sigma methodologies. * Manage supplier quality programs, ensuring compliance and continuous improvement within the supply chain. * Promote a culture of quality and innovation, providing training and guidance to teams worldwide. * Act as a key partner to engineering, operations, supply chain, and customer service in integrating quality across functions. * **Requirements** * Bachelor’s degree in Industrial Engineering or related field. * 6–8 years of experience in quality management, preferably in the industrial or manufacturing sector. * Proven leadership and multicultural team management experience. * Advanced knowledge of ISO and IATF standards, root cause analysis, statistical tools, and Lean principles. * Strong communication skills in Spanish and English (other languages are a plus). * Proficiency in ERP systems (SAP a plus) and MS Office. **We Offer** * Flexible schedule with Friday afternoons off. * Hybrid work model (office \+ 1 day remote). * Attractive benefits package. * Inclusive and collaborative company culture, where diversity and professional development are valued.

Carrer Martorell, 24, 08630 Abrera, Barcelona, Spain

Head Bartender645225129295371228

**Additional Information** **Job Number**25186846 **Job Category**Food and Beverage \& Culinary **Location**Hotel Arts Barcelona, Marina 19\-21, Barcelona, Spain, Spain, 8005 **Schedule**Full Time **Located Remotely?**N **Position Type** Non\-Management **POSITION SUMMARY** Ensure staff is working together as a team to ensure optimum service and that guest needs are met. Inspect grooming and attire of staff, and rectify any deficiencies. Complete opening and closing duties including setting up necessary supplies and tools, cleaning all equipment and areas, locking doors, etc. Inspect storage areas for organization, use of FIFO, and cleanliness. Complete scheduled inventories and stock and requisition necessary supplies. Monitor dining rooms for seating availability, service, safety, and well being of guests. Complete work orders for maintenance repairs. Assist management in hiring, training, scheduling, evaluating, counseling, disciplining, and motivating and coaching employees; and serve as a role model and first point of contact of the Guarantee of Fair Treatment/Open Door Policy process. Follow all company and safety and security policies and procedures; report accidents, injuries, and unsafe work conditions to manager; and complete safety training and certifications. Ensure uniform and personal appearance are clean and professional, maintain confidentiality of proprietary information, and protect company assets. Welcome and acknowledge all guests according to company standards, anticipate and address guests’ service needs, assist individuals with disabilities, and thank guests with genuine appreciation. Speak with others using clear and professional language. Develop and maintain positive working relationships with others, support team to reach common goals, and listen and respond appropriately to the concerns of other employees. Ensure adherence to quality expectations and standards; and identify, recommend, develop, and implement new ways to increase organizational efficiency, productivity, quality, safety, and/or cost\-savings. Read and visually verify information in a variety of formats (e.g., small print). Visually inspect tools, equipment, or machines (e.g., to identify defects). Stand, sit, or walk for an extended period of time or for an entire work shift. Move, lift, carry, push, pull, and place objects weighing less than or equal to 50 pounds without assistance. Grasp, turn, and manipulate objects of varying size and weight, requiring fine motor skills and hand\-eye coordination. Move through narrow, confined, or elevated spaces. Move up and down stairs and/or service ramps. Reach overhead and below the knees, including bending, twisting, pulling, and stooping. Perform other reasonable job duties as requested by Supervisors. PREFERRED QUALIFICATIONS Education: High school diploma or G.E.D. equivalent. Related Work Experience: At least 2 years of related work experience. Supervisory Experience: At least 1 year of supervisory experience. License or Certification: None *At Marriott International, we are dedicated to being an equal opportunity employer, welcoming all and providing access to opportunity. We actively foster an environment where the unique backgrounds of our associates are valued and celebrated. Our greatest strength lies in the rich blend of culture, talent, and experiences of our associates. We are committed to non\-discrimination on any protected basis, including disability, veteran status, or other basis protected by applicable law.* At more than 100 award\-winning properties worldwide, The Ritz\-Carlton Ladies and Gentlemen create experiences so exceptional that long after a guest stays with us, the experience stays with them. Attracting the world’s top hospitality professionals who curate lifelong memories, we believe that everyone succeeds when they are empowered to be creative, thoughtful and compassionate. Every day, we set the standard for rare and special luxury service the world over and pride ourselves on delivering excellence in the care and comfort of our guests. Your role will be to ensure that the “Gold Standards” of The Ritz\-Carlton are delivered graciously and thoughtfully every day. The Gold Standards are the foundation of The Ritz\-Carlton and are what guides us each day to be better than the next. It is this foundation and our belief that our culture drives success by which The Ritz Carlton has earned the reputation as a global brand leader in luxury hospitality. As part of our team, you will learn and exemplify the Gold Standards, such as our Employee Promise, Credo and our Service Values. And our promise to you is that we offer the chance to be proud of the work you do and who you work with. In joining The Ritz\-Carlton, you join a portfolio of brands with Marriott International. **Be** where you can do your best work, **begin** your purpose, **belong** to an amazing global team, and **become** the best version of you.

Ctra. Arrabassada - Camí de Sant Medir, 08196, Barcelona, Spain

Quality Engineer - Homologation Area (Temporary)645225128108821229

Quality Engineer - Homologation Area (Temporary)

**Company Description** **Company Description** ***Shaping the Future of Automotive Engineering*** Applus\+ IDIADA is a global leader in automotive engineering, offering a dynamic and rewarding career opportunity for professionals passionate about shaping the future of mobility. As a TOP Employer certified company with over 3500 professionals from more than 24 countries, we provide a diverse and inclusive work environment that fosters innovation and growth with colleagues from over 55 nationalities contributing to a safer, more efficient, and sustainable vehicles. **Why join us?** Enjoy a flexible hybrid work model in a company that takes care of the employees’ wellbeing, offering work\-life balance benefits such as subsidized canteen, free language courses, transport and coaching services. Join a company that has a deep commitment to sustainability and push yourself to reach your full potential in a dynamic and challenging setting that values innovation and expertise. ***Come \& join us on the road to success.*** \#LI\-Hybrid **Job Description** As Quality Engineer and member of the Homologation area, your mission will be to promote a culture of quality according to the Management Policy defined by the IDIADA Group. **Main functions:** * Collaborate with the development, maintenance and implementation of the QMS (ISO Certifications 9001, 14001 and 45001\) and ISO 17025, ISO 17020, ISO 17065 and ISO 17021\-1 Accreditations according to the IDIADA policy. * Guarantee the proper performance and update the Management System documentation (update procedures, processes, etc). * Collaboration with different departments for the correct implementation of the quality requirements defined in the QMS, with the object of improving the processes of the company. * Prepare and attend internal \& external audits. * Support the process owners audited to establish the necessary actions to solve the non\-conformities detected and to follow up the actions defined until verification of effectiveness. * Manage Non\-conforming work and Incident management with support of Quality, Environmental and OHS department. **Qualifications** Bachelor's Degree or Master's degree in Industrial, Aeronautics or Mechanical Engineering. Other education will be valued depending on the candidate's professional experience. **Languages** High level of English is mandatory. Other languages will be valued (French, German, Italian...). **Profile** * Knowledge in QMS standards (ISO9001, ISO17025\), OHSMS and EMS. * Knowledge in quality tools such as problem\-solving analysis, Kaizen and 5S method. * Proactive \& cooperative person * Client orientation * High level of MS office. * Passion for the work well done **Additional Information** Applus IDIADA is committed to **equality,** **diversity** and **inclusion**. We don’t put limits on you, so don’t put limits on yourself either. There is a place for everyone.

7H22+22 Santa Oliva, Spain

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