Igualada Freight/Cargo Forwarding Job Listings - OK

Browse

Property For Sale

Property For Rent

Antiques Collectibles

Baby Kids Items

Books， Movies And Music

Home Improvement Supplies

Musical Instruments

Office Supplies

Home Improvement

Repair And Technical Support

Writing， Translation， And Transcription

Administration & Office Support

Advertising， Arts & Media

Banking & Financial Services

Call Center & Customer Service

CEO & General Management

Community Services & Development

Consulting & Strategy

Design & Architecture

Education & Training

Farming， Animals & Conservation

Government & Defense

Healthcare & Medical

Hospitality & Tourism

Human Resources & Recruitment

Information & Communication Technology

Manufacturing， Transport & Logistics

Marketing & Communications

Mining， Resources & Energy

Real Estate & Property

Retail & Consumer Products

Science & Technology

Self Employment

Sport & Recreation

Trades & Services

Activities & Groups

Artists & Musicians

Classes & Lessons

Friendship & Networking

Travel & Travel Partners

Skills & Language Swap

···

Log in / Register

Freight/Cargo Forwarding in Igualada

Best Match

Filter·1

Freight/Cargo Forwarding

Igualada

Salary

Job Type

Workplace type

Unit

Location:Igualada

Category:Freight/Cargo Forwarding

IT Systems Technician and AI Development Specialist64842959073027120

IT Systems Technician and AI Development Specialist

IT Systems Technician and AI Development Specialist The Raimon Gaja Institute https://institutoraimongaja.com/ is opening a selection process to hire an IT Systems and AI Development Technician. We are seeking a technically skilled individual with an innovative mindset. You will support the Head of IT in the daily technical management of the department. **Key responsibilities include:** · Providing user support by resolving hardware or software incidents. · Configuring printers, PCs, and IP telephony terminals. · Supporting the systems and AI application development team. · Administering physical and virtual servers and networks. · Optimizing processes through advanced automation of existing web pages and IT systems. · Providing cross-functional support across multiple technological areas of the company. · Network management: configuring and maintaining telecommunications networks to ensure proper operation. · CRM and MOODLE support. · Proficiency in Zoom, Meet, and YouTube to assist with presentations, etc. · Database management. · **What we are looking for:** · A professional holding a Higher Vocational Training qualification in IT Systems or Application Development, with at least one year of experience in the duties described above. · **Mandatory: Knowledge of AI development and Python** · **Starting compensation:** 25,000€ gross per year · **Immediate start** Employment type: Full-time, permanent contract Salary: 25,000.00€–26,000.00€ per year Application questions: * Do you have experience in Python and AI? Work location: On-site

Carrer de Còrsega, 211, Eixample, 08036 Barcelona, Spain

€ 25,000-26,000/year

Global Clinical Program Lead, Radioconjugate Late Development Oncology64842936605442121

Global Clinical Program Lead, Radioconjugate Late Development Oncology

**Introduction to role:** ------------------------- Are you interested in pushing the boundaries of science and transform the lives of patients living with cancer? As a Global Clinical Program Lead, you'll be accountable for a significant portion of a late development oncology clinical program. This role involves managing complex clinical studies, often requiring collaboration with third parties, and demands strategic thinking and entrepreneurial spirit to maintain a competitive edge. You'll work closely with study physicians to design, conduct, monitor, and interpret data from clinical studies, ensuring they meet global market needs. As a catalyst for new ways of working, you'll lead process improvement projects and mentor staff, shaping the future of oncology clinical development. **Accountabilities:** --------------------- * Overall clinical and scientific content for the radioconjugate product or indication(s) aligned to GPT strategy. * Sets team vision and goals aligned to TALT and product strategy. * With the DCD, ensure the CPT rapidly implements new processes, systems, and learning. * Prioritization of clinical activities within the clinical program and ensures forward\-looking risk mitigation strategies. * Promotes cross\-functional, proactive, and solutions\-oriented team actions through end\-to\-end knowledge of oncology drug development. * Enables quick and effective troubleshooting within the CPT and its associated sub\-teams. * Mentors individual team members as needed, building future AZ talent through the matrix team model. * Single point accountable leader for the design, delivery, and interpretation of clinical studies ensuring ethical and scientific integrity. * Accountable for late phase study designs and study design concept delivery within their assigned oncology program of studies. * Provides strategic clinical and scientific knowledge to Study Physicians for initiation, execution, and completion of clinical studies. * Represents the company and delivers clinical information/answers to Regulators, Ethic Committees, Marketing Companies, investigators/sites. * Provides strategic clinical and scientific knowledge into development decision points/TPP/TPC and target labeling. * Works as a delegate of the Global Clinical Head across several oncology studies. * Can be the clinical representative on Global Product Teams for the assigned part of the program. * Ability to form and maintain an excellent reputation outside of AZ. * Trial conduct and hands\-on delivery accountabilities * Accountable to GCH or delegate for significant clinical aspects and design/delivery of studies. * Collaborates seamlessly with global colleagues at other R\&D sites. * May be accountable for identifying risks and proposing mitigation strategies for successful Phase II, III or IV studies. * Scientific clinical analytical accountabilities * Maintains up\-to\-date knowledge of relevant scientific literature. * Delivers analyses of clinical data in a balanced and statistically robust manner. * Functional and Project Leadership * Significant role in shaping the function through idea generation and leading improvement projects. * Seen as a role model in their function, providing hands\-on coaching and mentoring to staff. **Essential Skills/Experience:** -------------------------------- * Life Science\-based degree at masters or above (i.e. M.D., PHD, PharmD, Masters in Life Science\-based area) * 7\+ years clinical research expertise in oncology clinical development including study design, protocol development, monitoring and implementing clinical trials, interpreting and reporting trial results * Strong knowledge and understanding of the Oncology therapeutic area with experience in diverse biological mechanisms. * Proven track record of successful clinical delivery with demonstrated examples of strategic influence to clinical studies/programs * Explores positions and alternatives to reach agreements and solutions. Presents clear arguments to gain acceptance of ideas and influences outcomes to meet organizational objectives * Good knowledge of biostatistics, Clinical Development, global regulatory environment and pharmacovigilance and working knowledge of medical affairs and payer environment * Proven cross\-functional teamwork and collaboration skills * Excellent presentation skills. Can communicate effectively with internal and external collaborators **Desirable Skills/Experience:** -------------------------------- * MD \& PhD (or other complementary degree) in scientific discipline * Experience in radioconjugate clinical development programs * Late phase development experience preferred, especially within prostate cancer indications * Strong general medical knowledge * An understanding of pharmaceutical industry R\&D, particularly of major clinical milestones and factors influencing drug development * An understanding of the interplay between clinical, commercial objectives, drug safety, and regulatory requirements * Demonstrated ability to lead, coach, and mentor junior physicians/scientists 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. At AstraZeneca, you'll be part of a pioneering team dedicated to transforming cancer treatment through innovative approaches. With one of the broadest Oncology pipelines in the industry, you'll have opportunities to work on novel drugs that make a real difference in patient outcomes. Our collaborative environment fosters courage and curiosity, empowering you to take smart risks and challenge norms. We embrace diverse perspectives to tackle tough medical challenges together. Ready to make bold moves in oncology? Apply now to join our mission\-driven team!

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

Negotiable Salary

EFL Teacher / ESL Instructor / English Teacher64842298014209122

EFL Teacher / ESL Instructor / English Teacher

**Janet’s – School of English is searching for an EFL teacher to start in January with an indefinite contract. Our school is located in Castelldefels (5 min walk from the station, 25 min from Barcelona) and the position is to teach kids from 7 years old, teens and adults. 20 to 21h30min block hours from Monday to Friday in the afternoons. Gross monthly salary depending on qualifications \& proven experience: 1320\-1548€ \+ possibility to increase timetable/salary with private or company classes and also of increasing hours for next academic year reaching a salary of 1617\-1800€ for 25h/month gross aprox.** **Please send your CV and cover letter to hr@janets.es** **and we’ll get back to you shortly.** As a TEFL teacher at Janet's, you will be teaching kids, teens \& adults in a dynamic, communicative way with a selection of resources. Our course books are carefully chosen to enable us to create interesting and successful classes also allowing time for teacher's individual input which is considered to be of prime importance. **This position involves:** * Planning, preparing \& delivering lessons to a range of levels \& age groups. * Classroom management \& feedback to reception/direction/parents. * Preparing weekly homework for all groups. * Attending a monthly training (seminar, workshop, meeting). * Keeping attendance lists/records of work. * Reports: to be sent each term for kids \& teens, and twice per year with respect to adults. * Punctuality is of the utmost importance. **Requirements:** * Native level of English * TEFL, CELTA or DELTA * Legal documents to work in Spain * Experience teaching Cambridge English exams (desirable) **Thank you.** www.janets.es Job Types: Part\-time, Contract, Permanent Pay: 1,320\.00€ \- 1,548\.00€ per month Application Question(s): * Are you currentrly living in Castelldefels? Experience: * TEFL: 2 years (Preferred) Work Location: In person

Passatge de l'Espígol, 2, 08860 Castelldefels, Barcelona, Spain

€ 1,320-1,548/month

Global Viral and bacterial infections Programme Manager64842298092289123

Global Viral and bacterial infections Programme Manager

The Barcelona Institute for Global Health (ISGlobal) is a cutting\-edge institute addressing global public health challenges through research, translation into policy and education. ISGlobal has a broad portfolio in communicable and non\-communicable diseases including environmental and climate determinants, and applies a multidisciplinary scientific approach ranging from the molecular to the population level. Research is organized in five programs: Climate, Air Pollution, Nature and Urban Health; Environment and Health over the Lifecourse; Global Viral and Bacterial Infections; Malaria and Neglected Parasitic Diseases and Maternal Child and Reproductive Health. ISGlobal is accredited with the Severo Ochoa distinction, a seal of excellence of the Spanish Science Ministry. ### **WHAT WE ARE LOOKING FOR** ISGlobal is seeking a full\-time PROGRAMME MANAGER who is interested in supporting and managing activities of the Global Viral and Bacterial Infections Programme at ISGlobal. The activities in which the PROGRAMME MANAGER will be: * Coordination and promotion of interactions among the research groups integrated in the RP * Planning of the overall research objectives, scientific questions and challenges, needs and resources to achieve them * Reporting and Evaluation (including among others EAC, CERCA, internal) * Promote interactions across RP and with other departments to maximize impact * Internal and external communication Identification and promotion of strategic alliances ### **KEY RESPONSIBILITIES** * The key responsibility of the candidate will be to manage the general organization of the programme, and ensure that all the abovementioned tasks are correctly carried out. **AUXILIAR TASKS** This job description reflects the present requirements of the post but may evolve at any time in the future as duties and responsibilities change and/or develop providing there is appropriate consultation with the post\-holder. This job description is not a definitive or exhaustive list of responsibilities but identifies the key responsibilities and tasks of the post holder. The specific objectives of the post holder will be subject to review as part of the individual professional assessment process. ### **SKILLS** * Candidate with initiative and proactivity * Outstanding organizational and good teamworking skills. * Responsible, flexible and with problem solving skills. * Eager to learn, proactive and with great initiative * Demonstrable adaptability and flexibility to adapt positively to change * Previous experience in molecular microbiology The post holder will adhere to ISGlobal principles contained in **People management policy, including Equity, diversity and health safety**. The post holder will respect, and be accountable to ensure ISGlobal policies and procedures. ### **TRAINING AND EXPERIENCE / QUALIFICATIONS** * Previous management experience in the microbiology field (10 years). Compulsory to have a PhD on clinical microbiology. ### **LANGUAGE LEVEL** * Proficiency in Catalan, English, and Spanish. ### **CONDITIONS** * Duration: 16th January 2026 – 15th October 2026 * Starting date: 16/01/2026 * Contract Type: Full time * Salary: Technician I B ### **HOW TO APPLY** Applicants must fill in the request form and attach the CV and a Cover Letter. Each attached document must be named with the candidate name and surname. The receipt of applications will be open until 2nd of January 2025\. The interviews could be placed during the reception of candidatures period. Diverse candidatures are encouraged, that includes: gender, race, ethnicity, religion, age, sexual orientation, physical abilities, and political views. ### **SELECTION PROCESS** The selection process is designed in two phases: 1\- Interview phase of a technical nature, with the team that requires the incorporation. To assess the person's skills and CV. 2 \- Meeting with HR with the finalist(s) to finish assessing the profile and discuss contractual and institutional issues. If needed any technical test could be passed. A Psychological Competency Evaluation Test will be required for the structural or transversal positions. In accordance with the OTM\-R principles, a gender\-balanced recruitment panel is formed for every vacancy at the beginning of the process. After reviewing the content of the applications, the panel will start the interviews, with at least one technical and one administrative interview. A profile questionnaire as well as a technical exercise may be required during the process. *In ISGlobal we are committed to maintaining and developing a work environment in which the values and principles of our organization are respected and equal opportunities between women and men be promoted in each of the areas in which we operate, not tolerating discrimination based on criteria such as age, gender, marital status, race, ethnicity, functional diversity, political leanings, religion, sexual orientation, gender identity or gender expression.* *We confirm our commitment towards the value of the diversity of our staff and student population and seek to promote peace, equity, diversity and inclusion as essential elements in contribution to improving health worldwide.*

Carrer del Rosselló, 153, Eixample, 08036 Barcelona, Spain

Negotiable Salary

Kitchen Cleaning Staff - Sarrià-Sant Gervasi Area64842254482177124

Kitchen Cleaning Staff - Sarrià-Sant Gervasi Area

Compass Group España is part of Compass Group PLC, the global leader in Foodservice and Support Services. For over 50 years, we have provided our services across key sectors including Business & Industry, Healthcare, Seniors, Education, Sports & Leisure, and Catering, with a portfolio of market-recognized brands. We rank among the world’s top 10 employers, with a team of 600,000 people across 50 countries, serving approximately 4 billion meals annually and working daily with 40,000 clients. Throughout these years, our team has consistently upheld its commitment to our clients, service quality, and innovative spirit. The Compass success formula: experience, trust, commitment, and the best team of professionals. If you wish to share our vision, join this great team. Eurest Colectividades S.L. guarantees equal opportunities and fair evaluation of all applications submitted for this selection process. Responsibilities \- Cleaning in kitchen and office * Plating cold and hot dishes. * Dishwashing line * Waste disposal Requirements \- Residence in the Sarrià-Sant Gervasi area — Barcelona * Experience working as ASL (Auxiliary Service Laborer) in collective catering and/or restaurant kitchens Offer Temporary contract to cover vacations from December 29 to January 12, with potential for permanent placement Full-time position Working hours: Monday to Friday, 3:00 PM to 11:00 PM Salary: Collective Agreement for Collective Catering — €1,430.53 gross per month, paid in 14 installments

Carrer de Pomaret, 98I, Sarrià-Sant Gervasi, 08017 Barcelona, Spain

€ 1,430/month

SEO Content Writer Internship - Italian64842254042242125

SEO Content Writer Internship - Italian

About Emagister: Our Mission Are you looking for an internship experience that truly makes a difference? Emagister is waiting for you! We are an internationally leading company in online education services, with a simple yet powerful mission: to connect millions of people with learning that will transform their lives. For years, we have made education accessible to everyone. Our culture: We are a dynamic, flexible, innovative team—and above all, people-oriented. If you identify with these values and are seeking a place where you can grow, learn at startup speed, and make a tangible digital impact, Emagister is the right place for you! We are looking for: Digital Content Writer Intern (Barcelona) This is your opportunity to take a major step into the digital world and build your career as a Content Creator. You won’t just be “uploading content”: under the guidance of our Digital Marketing team, you’ll learn how to create real impact. Your missions for impact and learning will include: - Targeted content creation: You will be responsible for uploading, updating, and optimizing content for SEO; researching audiovisual materials and reviews that capture our audience’s attention and improve our search engine rankings. - Strategic optimization: You will participate in optimizing the Reviews project and Quality Assurance (QA) processes, learning how to ensure content meets our standards of value. - Community building: You will foster active participation from thousands of users by managing reviews, thereby building a valuable database for our ecosystem. - Design and campaigns: You will support the design and creation of engaging promotional materials for various digital campaigns. - Project management: You will learn how to strategically manage user review acquisition. **Why Emagister is the best choice?** We care deeply about your well-being and your future. Here’s what we offer: - Paid internship: €800 gross per month. - Mentoring and development: Immerse yourself in a culture of continuous learning, with direct mentoring to accelerate your digital career. - Flexible hours: Intensive Fridays (8:00 AM–3:00 PM) and reduced hours in July and August to enjoy summer. - Hybrid model: The ideal balance between remote work (one day per week) and the energy of in-office teamwork. If your mission is to grow in Content Marketing, this is your chance! Job type: Full-time Application questions: * Do you live in Barcelona? Work location: On-site employment

Av. Alcalde Barnils, 70, 08174 Sant Cugat del Vallès, Barcelona, Spain

School Cafeteria Monitor in Montcada i Reixac64841265910530126

School Cafeteria Monitor in Montcada i Reixac

Compass Group España is part of Compass Group PLC, the global leader in Foodservice and Support Services. For over 50 years, we have provided our services across key sectors including Business & Industry, Healthcare, Seniors, Education, Sports & Leisure, and Catering, with a portfolio of market-recognized brands. We rank among the world’s top 10 employers, with a team of 600,000 people across 50 countries, serving approximately 4 billion meals annually and working daily with 40,000 clients. Throughout these years, our team has consistently upheld its commitment to clients, service quality, and an innovative spirit. The Compass success formula: experience, trust, commitment, and the best team of professionals. If you wish to share our vision, join this great team. Eurest Colectividades S.L. guarantees equal opportunities and fair evaluation of all applications submitted for this selection process. Responsibilities Responsibilities: * Provide support as needed at different schools to cover absences or substitutions during December/January 2025/2026. * Supervise and engage students during lunchtime. * Support the educational project. Requirements - Prior educational experience working with children, e.g., as a cafeteria or leisure-time monitor. * CURRENT SEXUAL OFFENSES CERTIFICATE, issued within the last 3 months. * Availability for immediate start. * Commitment until the end of the academic year. Offer Offer: * Weekly working hours: 10 to 12.5 hours, Monday to Friday, scheduled between 12:00 and 15:00. * Temporary contract for the 2025/2026 academic year. * Salary according to the Leisure-Time Monitor collective agreement.

Les Malves, 258, 08110 Montcada i Reixac, Barcelona, Spain

Negotiable Salary

Operator for Automotive Parts Inspection64841265704322127

Operator for Automotive Parts Inspection

**Description:** ---------------- At Logística e Ingeniería de Servicios S.L., we specialize in outsourcing industrial processes and plants, developing customized projects that improve operational efficiency. Logística e Ingeniería de Servicios S.L. is seeking 2 OPERATORS FOR INSPECTION for a company located in Sant Joan Despí (Barcelona). Responsibilities: * Quality control: ensuring the final product meets the end customer’s quality standards. * Visual inspection of finished parts. * Reporting daily production output, specifying OK and NOK parts (with defects identified). WE OFFER: * Immediate hiring. * Rotating shifts: 6–14 / 14–22. * Temporary contract for 2 months, with possibility of renewal. * Salary: €21,382 gross per year for the first three months. If this fits you, APPLY NOW! **Requirements:** --------------- * Good eyesight. * Ability to withstand constant and repetitive movements. * Personal vehicle.

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

€ 21,382/year

Forklift Operator Martorell64841265719555128

Forklift Operator Martorell

**Description:** ---------------- At Logística e Ingeniería de Servicios S.L., we specialize in outsourcing industrial processes and plants, developing customized projects that enhance operational efficiency. Logística e Ingeniería de Servicios S.L. is seeking 3 Forklift Operators for a company located in Martorell (Barcelona). Responsibilities: * Operating front-end forklifts. * Storing goods in the warehouse at a height of 6 meters. * Supplying production lines. WE OFFER: * Start date: 07/01/2026. * Rotating shifts: 6 a.m.–2 p.m. / 2 p.m.–10 p.m. / 10 p.m.–6 a.m. * Permanent contract with a 2-month trial period. * Salary: €22,875 gross/year. If this fits you, APPLY NOW! **Requirements:** --------------- * Good eyesight. * Valid forklift operator license is mandatory. * Personal vehicle.

FW8M+M8 Martorell, Spain

€ 22,875/year

Support Monitor for MONTBLANC. Ref. SMNTR64841265688451129

Support Monitor for MONTBLANC. Ref. SMNTR

**Description:** ---------------- At Serunion, a collective catering company with over 30 years of experience in the sector and a market leader, we are seeking top talent to join our centers. If you have relevant experience and are looking for an opportunity to demonstrate your skills, this position is perfect for you! **We are seeking a STUDENT SUPPORT MONITOR WITH SPECIAL EDUCATIONAL NEEDS (SEN) in MONTBLANC to fill a VACANCY starting 08/01/2026 at ESCOLA LES MURALLES** *At Serunion, we aim to build a diverse and committed team where everyone has the opportunity to develop their potential and contribute to our company’s success. We encourage you to apply and become part of our inclusive team!* **FUNCTIONS AND RESPONSIBILITIES:** * Accompanying and assisting children and/or young people with special educational needs. * Fostering the autonomy of these children and/or young people. * Assisting with mobility-related tasks, monitoring posture control and correcting it when necessary to maximize students’ mobility. * Encouraging students’ autonomy and self-management skills. * Remaining constantly attentive while working with children. * Promoting children’s active participation in various daily tasks, taking into account their individual limitations. * In general, ensuring students’ safety and comfort during their time at school/institute and supporting teachers/professors both inside and outside the classroom, in accordance with the Center’s Management directives. **SCHEDULE:** 5 hours/week Mondays and Wednesdays, from 12:30 to 15:00 **REQUIREMENTS:** * Certificate of Absence of Sexual Offences (valid until at least September 2025). * Training and/or experience in education or leisure activities. * Advanced Catalan. **SALARY:** As per collective agreement. **Once you apply for this position, you will receive a WhatsApp message containing a link to complete your virtual interview quickly and easily with DANI. Please stay alert and prepare for the next step in your professional journey with Serunion!** At Serunion, we aim to build a diverse and committed team where everyone has the opportunity to develop their potential and contribute to our company’s success. We encourage you to apply and become part of our inclusive team! **Requirements:** --------------- * Qualifications in leisure and/or education, as well as prior experience working with children with special educational needs, will be valued. * A valid Certificate of Absence of Sexual Offences, updated as of January 2025, is mandatory. * Advanced Catalan.

Carrer de la Civaderia, 18A, 43400 Montblanc, Tarragona, Spain

Negotiable Salary

Senior Regulatory Affairs Director648412655447051210

Senior Regulatory Affairs Director

Are you a strategically focussed Regulatory professional and would like to play an integral part in bringing life changing Oncology medicines to patients? If you are please read on! **About AstraZeneca** At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person. **Oncology Regulatory Science and Strategy** Within Oncology Regulatory Science and Strategy (ORSS) we bring hope and solutions to patients with unmet needs across the globe. As Regulatory professionals working on Oncology products, we work in areas of unmet need and take innovative regulatory approaches to bring life\-changing treatments to patients. We work across our pipeline and the business to get medicines to patients as efficiently and effectively as possible. The **Senior Regulatory Affairs Director** (SRAD) serves as the Franchise Global Regulatory Lead (GRL) developing and implementing the **global** strategy on complex **oncology** programs with multiple indications. In addition, the SRAD has the ability to function in dual capacity by serving as the regional lead based on location. The SRAD establishes external relationships with key stakeholders, leveraging these to maintain competitive advantage. You will be viewed as a senior leader within the Regulatory community. **What you’ll do** * Lead a Global Regulatory Strategy Team (GRST) of GRLs within the franchise, contributing members from the regions, emerging markets, RA CMC, Labelling and members of the submission and execution team. * Ensure that the strategy is crafted to deliver approval with competitive labelling in keeping with the properties of the product(s) and the needs identified by the business, markets and patients. * Lead the assessment of emerging data against aspirations and update Leadership on project risks/mitigation activities. * Represent Regulatory Affairs on Global Product Teams (GPTs) providing strategic advice and accountable for all regulatory activities. * Own the delivery of all milestones on your team including assessment of the probability of regulatory success based on a detailed assessment of risks and mitigations. * Demonstrate strategic leadership skills thereby contributing to effective product development. * Promote novel regulatory initiatives internally and engage externally on the corresponding topics. Lead the development of novel tools and technology. * Partner and influence developing views/guidance on a global scale. **Education, Qualifications, Skills and Experience** **Essential for the role:** * An advanced degree in a science related field and/or other appropriate knowledge/experience. * Previous demonstrated experience of regulatory drug development including product approval/launch. Successful leadership to at least one major regulatory approval at a global level including leading response team and labeling negotiations is desired. * Previous experience in leading major health authority interactions. * Solid knowledge of regulatory affairs within several therapeutic areas in early and late development. * Broad background of experience working in pharmaceutical business and prior experience in several areas within regulatory affairs. Experience in relevant therapy area (small molecules \& biologics) is preferred. * Proven leadership experience. * Ability to think strategically and critically and evaluate risks to regulatory activities. * Deep understanding of global regulatory science and will integrate with project strategy. You have a long standing experience of overall drug/biologic development processes and strategies for high profile, complex or novel development programs. **Desirable for the role:** * Previous experience with FDA advisory committee and EMA oral explanation hearings would be a plus * Previous experience working on due diligence activities and in a business alliance environment. * Ability to work strategically within a complex, business critical and high\-profile development program. **Why AstraZeneca?** At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We’re on an exciting journey to pioneer the future of healthcare. **So, what’s next?** Are you already imagining yourself joining our team? Good, because we can’t wait to hear from you! **Competitive salary and benefits package on offer.** The successful candidate will have access to a flexible employee benefits fund, including holiday purchase and flexible time off, pension contributions, Share Save plans, A performance recognition scheme and a competitive, generous remuneration package. **Where can I find out more?** Our Social Media, Follow AstraZeneca on LinkedIn Follow AstraZeneca on Facebook Follow AstraZeneca on Instagram

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

Negotiable Salary

Global Safety Program Lead648412655616031211

Global Safety Program Lead

**This is what you will do:** The Global Safety Program Lead, Senior Director is accountable to the Global Safety Head for the safety strategy, delivery, and oversight of the assigned asset(s); the professional will work with safety physicians and scientists responsible for the development, implementation, and application of safety strategy at asset and study level. Acts strategically to generate opportunity and value for the asset or indication to optimize benefit risk and maintain a competitive advantage. Line manages a team of safety physicians and / or scientists. They will be required at times to deputise for the Global Safety Head. The Global Safety Program Lead, Senior Director will operate according to the highest ethical, quality and compliance standards in compliance as provided by global and local regulations, GxP practice and AZ procedures. **You will be responsible for:** **Safety Expert** * Accountable for the overall scientific and clinical safety content for the assigned asset(s) or indications. * Accountable for the implementation and the high quality delivery of the Safety \& Strategy Management Team (SSaMT) and Safety Surveillance Team for assigned asset(s). * Responsible for overall safety content for the product or indication(s) aligned to GPT strategy. Sets safety team goals aligned to TA and product strategy. * For the assigned asset(s), accountable for safety TPP, Safety Go/No Go criteria, safety communication/messaging and the guidelines for toxicity management of the asset * Is accountable for project representation for Global Patient Safety at governance and other forums where safety is involved, eg DRC, eCRC, SARB, FSIRB, and DSMB/DMC, Medical Affairs Review Committees (MARC), product teams such CPT and GPT and Advisory Board meetings in partnership with GSH. * Accountable for the quality of key safety deliverables e.g., Risk Management Plans (RMPs) and Periodic Safety Reports (PSRs), compliance and adherence to PV regulations of the assigned asset(s). * Leads response to complex technical issues for specific safety aspects for the assigned asset(s). * Is accountable for safety contribution to study designs and study concept delivery within their assigned program * Through integrated understanding of the product strategy, provides strategic safety knowledge and support to the safety medical directors and scientists through initiation, execution, and completion of the clinical programs for the assigned asset(s). * Leads the safety physicians and scientists to support the safety strategy and input into the program design, monitoring, and data interpretation from pre\-clinical and clinical studies, communication and post\-marketing surveillance, epidemiology, pre\-clinical and literature, epidemiology for each asset. * Ensures that own work and work of team is compliant with Safety Health and Environment (SHE) standards and all other relevant internal and external regulations and standards. * Represents the Company and accountable for the quality of safety delivery e.g., regulatory submissions, answers to Health Authority Queries, Ethic Committees, Marketing Companies, investigators/sites, and provides clarifications as well as solves safety issues in the study team. * May be required to support in\-licensing opportunities. * Promotes and enables cross\-functional, proactive and solutions\-orientated team actions and behaviours * Accountable for implementation of new processes, systems and learning, including new ways of working. * Prioritizes risk mitigation strategies and effective trouble shooting. * Line manages a team of safety physicians and / or scientists. **Scientific clinical safety analytical accountabilities** * Maintains up\-to\-date knowledge of the relevant safety scientific literature, and is able to clearly communicate key impactful information, * Accountable for proper data collection and interpretation for determination of the risks and inform the label in markets globally * Delivers analyses of clinical safety data in a balanced and statistically robust manner, to drive interpretations and develop novel proposals. * Serves as a source of scientific and clinical safety knowledge for the Product Team, in the analyses and interpretation of scientific and clinical safety data. **You will need to have:** * Medical degree or equivalent degree in biomedicine or science * 5 years extensive relevant clinical, safety and risk management experience in the pharmaceutical, biotech, CRO industry, academia or Health Authorities * Proven track record of successful clinical safety delivery with demonstrated examples of strategic influence to clinical studies/programs. * Ability to collaborate across a matrixed environment and influence cross\-functional\- leaders on decision\-making (e.g. Clinical Development, Medical Affairs, Regulatory Affairs). * Thorough knowledge and understanding of pharmacovigilance \& safety deliverables, standards and processes at a global level; including pre and post launch experience. * Experience of global regulatory submissions and interacting with major regulatory agencies. * Demonstrated ability to successfully lead, coach, and mentor other safety medical directors/scientists. * Available to travel domestically and internationally * Demonstrated ability to present complex topics to senior leaders at safety and development governances for alignment and endorsement. **We would prefer for you to have:** * PhD (or other complementary degree) in scientific discipline. * Excellent, independent judgment based on leading\-edge knowledge and expertise. * Excellent speaking skills, industry conference speaking experience. * Excellent, independent judgment based on knowledge and expertise. * Demonstrated clinical safety and research expertise in an appropriate disease area.

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

Negotiable Salary

Senior Accountant648412656107551212

Senior Accountant

We are **Impress**. We believe everyone deserves a smile they’ll love. We are the largest chain of ortho clinics with fully digital processes. We have revolutionized the invisible orthodontic sector with the best team of professionals specialized in making people smile and using the latest technology for the diagnosis, treatment, and follow\-up of all cases. Born in Barcelona in 2019, in just 6 years, we’ve grown to pioneer leading care, flagship clinics and state\-of\-the\-art tech across 10 countries and more than 150 locations, and we are expanding fast! Our aim is to improve people’s health and quality of life across the globe. We are looking for a **Senior Accountant** to join our Finance department from the office in Barcelona. If you have a solid knowledge of GL accounting, experience in accounts reconciliation, and want to join a collaborative and global team, apply now! This is your opportunity to experience a \#1 health\-tech start\-up where both your work and your results are highly tangible and matter to the business. **Responsibilities:** * Take care of statutory accounting and tax accounting for the designated area. * Perform daily, weekly, monthly, quarterly, and annual accounting activities, including but not limited to journal entries, reconciliations, and reporting. * Prepare the information for filing monthly, quarter and yearly taxes and other miscellaneous filings. * Act as a liaison with business partners by answering inquiries and explaining accounting procedures. * Record, create and distribute invoices for monthly fees and royalties, set\-up ACH files for collections, maintain Accounts Receivable (A/R) balances. * Drive Accounts Receivable and Accounts Payable accounting best practices. * Support \& drive processes implementation and improvement. * Support \& drive design of accounting policies and procedures. * Work with internal and external auditors where required. * Provide support for the integration of the new ERP/Finance System. * Participate in ad hoc analytics, projects, and initiatives. * Act as senior subject matter expert in accounting matters. **Requirements:** * **English: Professional proficiency. Spanish and any languages are a big plus.** * 4\+ Years of Professional Experience as an Accountant * Proven experience in a similar role, ideally in a large\-scale global start\-up or Big 4 audit firm. * Bachelor's or associate's degree in accounting, or a related specialization. * In\-depth knowledge of accounting rules and regulations. * Advanced level in Excel. **What we offer:** * Opportunity to grow in an innovative company and Top International Scale Up. * Attractive Compensation package. * Benefits with our treatments, aligners, and products. * Collaborative work environment and positive culture. * International and diverse teams. * Coffee and fresh fruit every morning. * Access to our Gym *At Impress we cultivate a culture of inclusion and diversity. We celebrate our employees' individual strengths, views, and experiences and we encourage all candidates to apply, without regard to race, color, religion, gender identity, sexual orientation, age, national origin, disability, or any other factor.* *Our differences enable us to be a better team – one that makes better decisions, drives innovation, and delivers better results.* Job Type: Full\-time Pay: 40,000\.00€ per year Application Question(s): * How many years of experience do you have working with Spanish GAAP ? Work Location: In person

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

€ 40,000/year

Senior Accountant - Spanish GAAP648412656279061213

Senior Accountant - Spanish GAAP

We are **Impress**. We believe everyone deserves a smile they’ll love. We are the largest chain of ortho clinics with fully digital processes. We have revolutionized the invisible orthodontic sector with the best team of professionals specialized in making people smile and using the latest technology for the diagnosis, treatment, and follow\-up of all cases. Born in Barcelona in 2019, in just 6 years, we’ve grown to pioneer leading care, flagship clinics and state\-of\-the\-art tech across 10 countries and more than 150 locations, and we are expanding fast! Our aim is to improve people’s health and quality of life across the globe. We are looking for a **Senior Accountant** to join our Finance department from the office in Barcelona. If you have a solid knowledge of GL accounting, experience in accounts reconciliation\-Spanish GAAP, and want to join a collaborative and global team, apply now! This is your opportunity to experience a \#1 health\-tech start\-up where both your work and your results are highly tangible and matter to the business. **Responsibilities:** * Take care of statutory accounting and tax accounting for the designated area. * Perform daily, weekly, monthly, quarterly, and annual accounting activities, including but not limited to journal entries, reconciliations, and reporting. * Prepare the information for filing monthly, quarter and yearly taxes and other miscellaneous filings. * Act as a liaison with business partners by answering inquiries and explaining accounting procedures. * Record, create and distribute invoices for monthly fees and royalties, set\-up ACH files for collections, maintain Accounts Receivable (A/R) balances. * Drive Accounts Receivable and Accounts Payable accounting best practices. * Support \& drive processes implementation and improvement. * Support \& drive design of accounting policies and procedures. * Work with internal and external auditors where required. * Provide support for the integration of the new ERP/Finance System. * Participate in ad hoc analytics, projects, and initiatives. * Act as senior subject matter expert in accounting matters. **Requirements:** * **English: Professional proficiency. Spanish and any languages are a big plus.** * 4\+ Years of Professional Experience as an Accountant. * Experience Spanish GAAP * Proven experience in a similar role, ideally in a large\-scale global start\-up or Big 4 audit firm. * Bachelor's or associate's degree in accounting, or a related specialization. * In\-depth knowledge of accounting rules and regulations. * Advanced level in Excel. **What we offer:** * Opportunity to grow in an innovative company and Top International Scale Up. * Attractive Compensation package. * Benefits with our treatments, aligners, and products. * Collaborative work environment and positive culture. * International and diverse teams. * Coffee and fresh fruit every morning. * Access to our Gym *At Impress we cultivate a culture of inclusion and diversity. We celebrate our employees' individual strengths, views, and experiences and we encourage all candidates to apply, without regard to race, color, religion, gender identity, sexual orientation, age, national origin, disability, or any other factor.* *Our differences enable us to be a better team – one that makes better decisions, drives innovation, and delivers better results.* Job Type: Full\-time Pay: 40,000\.00€ \- 45,000\.00€ per year Application Question(s): * How many years of experience do you have working with Spanish GAAP ? Work Location: In person

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

€ 40,000-45,000/year

Global Clinical Program Lead648412655287071214

Global Clinical Program Lead

**Introduction to role:** ------------------------- Are you interested in pushing the boundaries of science and transform the lives of patients living with cancer? As a Global Clinical Program Lead, you'll be accountable for a significant portion of a late development oncology clinical program. This role involves managing complex clinical studies, often requiring collaboration with third parties, and demands strategic thinking and entrepreneurial spirit to maintain a competitive edge. You'll work closely with study physicians to design, conduct, monitor, and interpret data from clinical studies, ensuring they meet global market needs. As a catalyst for new ways of working, you'll lead process improvement projects and mentor staff, shaping the future of oncology clinical development. **Accountabilities:** --------------------- * Overall clinical and scientific content for the product or indication(s) aligned to GPT strategy. * Sets team vision and goals aligned to TALT and product strategy. * With the DCD, ensure the CPT rapidly implements new processes, systems, and learning. * Prioritization of clinical activities within the clinical program and ensures forward\-looking risk mitigation strategies. * Promotes cross\-functional, proactive, and solutions\-oriented team actions through end\-to\-end knowledge of oncology drug development. * Enables quick and effective troubleshooting within the CPT and its associated sub\-teams. * Mentors individual team members as needed, building future AZ talent through the matrix team model. * Single point accountable leader for the design, delivery, and interpretation of clinical studies ensuring ethical and scientific integrity. * Accountable for late phase study designs and study design concept delivery within their assigned oncology program of studies. * Provides strategic clinical and scientific knowledge to Study Physicians for initiation, execution, and completion of clinical studies. * Represents the company and delivers clinical information/answers to Regulators, Ethic Committees, Marketing Companies, investigators/sites. * Provides strategic clinical and scientific knowledge into development decision points/TPP/TPC and target labeling. * Works as a delegate of the Global Clinical Head across several oncology studies. * Can be the clinical representative on Global Product Teams for the assigned part of the program. * Ability to form and maintain an excellent reputation outside of AZ. * Trial conduct and hands\-on delivery accountabilities * Accountable to GCH or delegate for significant clinical aspects and design/delivery of studies. * Collaborates seamlessly with global colleagues at other R\&D sites. * May be accountable for identifying risks and proposing mitigation strategies for successful Phase II, III or IV studies. * Scientific clinical analytical accountabilities * Maintains up\-to\-date knowledge of relevant scientific literature. * Delivers analyses of clinical data in a balanced and statistically robust manner. * Functional and Project Leadership * Significant role in shaping the function through idea generation and leading improvement projects. * Seen as a role model in their function, providing hands\-on coaching and mentoring to staff. **Essential Skills/Experience:** -------------------------------- * Life Science\-based degree at masters or above (i.e. M.D., PHD, PharmD, Masters in Life Science\-based area) * 7\+ years clinical research expertise in oncology clinical development including study design, protocol development, monitoring and implementing clinical trials, interpreting and reporting trial results * Strong knowledge and understanding of the Oncology therapeutic area with experience in diverse biological mechanisms. * Proven track record of successful clinical delivery with demonstrated examples of strategic influence to clinical studies/programs * Explores positions and alternatives to reach agreements and solutions. Presents clear arguments to gain acceptance of ideas and influences outcomes to meet organizational objectives * Good knowledge of biostatistics, Clinical Development, global regulatory environment and pharmacovigilance and working knowledge of medical affairs and payer environment * Proven cross\-functional teamwork and collaboration skills * Excellent presentation skills. Can communicate effectively with internal and external collaborators **Desirable Skills/Experience:** -------------------------------- * MD \& PhD (or other complementary degree) in scientific discipline * Strong general medical knowledge * An understanding of pharmaceutical industry R\&D, particularly of major clinical milestones and factors influencing drug development * An understanding of the interplay between clinical, commercial objectives, drug safety, and regulatory requirements * Demonstrated ability to lead, coach, and mentor junior physicians/scientists 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. At AstraZeneca, you'll be part of a pioneering team dedicated to transforming cancer treatment through innovative approaches. With one of the broadest Oncology pipelines in the industry, you'll have opportunities to work on novel drugs that make a real difference in patient outcomes. Our collaborative environment fosters courage and curiosity, empowering you to take smart risks and challenge norms. We embrace diverse perspectives to tackle tough medical challenges together. Ready to make bold moves in oncology? Apply now to join our mission\-driven team!

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

Negotiable Salary

Data Generation Specialist647496963338251215

Data Generation Specialist

**G+D makes life safer for billions of people worldwide. We build trust in the digital age with integrated security technologies across three business areas: Digital Security, Financial Platforms, and Monetary Technology. For over 170 years, we have been a trusted partner to our customers with innovative SecurityTech solutions! We are an international technology group and a traditional family-owned company with more than 14,000 employees in 40 countries. Building Trust is our path to success. Trust is the foundation of our collaboration at G+D.** **In Payment Technology, our mission is to be at the beginning of every transaction—making it secure and seamless. We also develop contemporary payment and banking solutions for our digital era. As a single point of contact, we produce and personalize hundreds of millions of payment cards each year and store their "digital twins"—mobile and digital. Would you like to actively shape the digital transformation with us?** **G+D Mobile Security**, a leader in SmartCards and Secure Payment Elements (credit cards, SIM/eSIM, vehicles, smartphones, wearables), is seeking a **Data Generation Specialist** to join our **Customization** team in El Prat de Llobregat, Barcelona, with international scope. This position is critical to ensuring correct data generation and validation for banking client projects, guaranteeing that card personalization processes are executed optimally and securely. **What will your mission be?** Contribute to the end-to-end lifecycle of client projects, focusing on the data generation service: configuration, validation, documentation, monitoring, and maintenance of production systems and environments, as well as providing continuous technical support. **What will you do daily?** ------------------------------- * Manage data generation projects across production environments, including unit, system, and acceptance testing. * Validate and adjust incoming data for card personalization, including returning data to the client when required. * Monitor and maintain data processing systems and environments. * Maintain databases and generate statistical reports. * Provide support to production centers and other teams on issues, implementations, and rollouts. * Prepare data and physical samples for internal use, clients, and certifications. * Complete project documentation and comply with change management processes. * Coordinate with internal teams (Customization, R&D, Process Engineering, CPM, etc.) to ensure timely and accurate deliverables. * Comply with internal and external regulations (ISO, PCI, VISA, MASTERCARD, EMVCO, etc.) and applicable data protection legislation. **What are we looking for?** ------------------ **Your human side:** * Positive, proactive attitude with strong teamwork orientation. * Ability to manage multiple projects and adapt to dynamic environments. **Your experience and knowledge:** * Technical education (preferably higher vocational training in IT). * Fluent English (spoken and written). * Proficiency in Windows environments. * Recommended: SQL and technical support experience (Level 1 or 2). * Valuable experience with tools such as Confluence, Jira, Bitbucket, Ansible. * Availability for on-site work and shift-based schedules. **What do we offer?** ------------------- * **International environment**: Collaborate with global teams on innovative projects. * **Inclusive culture**: A diverse, flat-hierarchy, people-oriented workplace. * **Professional development**: Continuous training and growth opportunities. * **Benefits**: Flexible compensation (health insurance, transport allowance, training, childcare vouchers), on-site parking and cafeteria. * **Location**: El Prat de Llobregat, well-connected by public transport (Bus 88, 110, Metro L10 ZAL–Riu Vell, PR4) or private vehicle. **Privacy Notice** ------------------ The personal data you provide will be processed to manage your application in accordance with the GDPR and our Privacy Policy, available at Data Privacy | G+D.### ### **A look behind the scenes** ### **Contact** **HR Team Spain** seleccion.gdi@gi-de.com ### **JOB OFFER****Job Details** --------------- **Job Title** Data Generation Specialist **Business Sector** Giesecke + Devrient ePayments Iberia S.A C/ 114 nº 27 Polígon Pratenc **Requisition ID** 26340 **Location** Prat de Llobregat (BCN), ES **Career level** Experienced **Job Type** Full-time, Permanent contract Shift work **Contact** HR Team Spain seleccion.gdi@gi-de.com We are an organization committed to equal opportunity. We promote diversity in all its forms and cultivate an inclusive, prejudice-free, non-discriminatory, and harassment-free workplace where all employees feel valued and part of the community. We welcome all applications, regardless of gender, age, race, ethnic origin, social or cultural background, religion, disability, or sexual orientation.

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

Negotiable Salary

Data Processing Specialist647496963182111216

Data Processing Specialist

**G+D makes the lives of billions of people worldwide safer. We build trust in the digital age with integrated security technologies across three business areas: Digital Security, Financial Platforms, and Monetary Technology. For over 170 years, we have been a trusted partner to our customers with innovative SecurityTech solutions! We are an international technology group and a traditional family-owned company with more than 14,000 employees in 40 countries. Building Trust is our path to success. Trust is the foundation of our cooperation at G+D.** **In Payment Technology, our mission is to be at the beginning of every transaction—making it secure and simple. We also create contemporary payment and banking solutions for our digital era. As a single point of contact, we produce and personalize hundreds of millions of payment cards annually and store their "digital twins"—mobile and digital. Would you like to actively shape the digital transformation with us?** At G+D Mobile Security—the global leader in security solutions for payments and identity (credit cards, SIM/eSIM, smartphones, vehicles, wearables)—we are seeking a Data Processing Engineer to join our team in El Prat de Llobregat, Barcelona, where we develop proprietary products that ensure protection of confidential data and secure services for global clients (telecom operators, banks, device manufacturers, automotive companies, etc.). **What will be your mission?** ------------------------- Participate in the full project development lifecycle for clients, focusing on data and cryptographic key processing: requirements analysis, functional and technical design, programming, configuration, testing, documentation, implementation, and ongoing technical support. Your goal will be to ensure secure and efficient data personalization for our clients. **What will you do on a day-to-day basis?** ------------------------------- * Analyze and define technical and functional requirements for new projects. * Configure and parameterize systems to reflect customer needs. * Implement scripts and customizations to meet specific requirements. * Validate and adjust incoming data to ensure its quality. * Migrate code between platforms and environments, ensuring compatibility. * Conduct unit, system, and user acceptance testing. * Configure processes and prepare packages for production personalization. * Maintain databases and generate statistical reports. * Provide support to production centers and handle second-level incidents. * Document projects and follow change management processes. * Coordinate with internal teams (R&D, process engineering, CPM, etc.) to meet deadlines and standards. * Ensure compliance with internal and external regulations (ISO, PCI, VISA, MASTERCARD, EMVCO, etc.) and applicable data protection legislation. **What are we looking for?** ------------------ **Your human side:** * Positive, proactive attitude and strong team orientation. * Ability to manage multiple projects and adapt to dynamic environments. **Your experience and knowledge:** * Technical education: Advanced Vocational Training (CFGS) or Bachelor’s degree in Computer Engineering or equivalent. * Familiarity with Windows environments. * Object-oriented programming (C#, .NET preferred). * Experience with databases and SQL queries. * Fluent English (spoken and written). * Experience with tools such as Confluence, Jira, Bitbucket, Ansible is desirable. * Familiarity with technical documentation (specifications, guidelines, test plans). * Knowledge of the data processing sector (desirable). **What do we offer?** ------------------- * **Culture and team:** Dynamic, collaborative, and friendly environment. * **Active participation:** Your voice matters—you can propose ideas and improvements. * **Schedule and work-life balance:** Morning and afternoon shifts, hybrid working model. * **Contract and benefits:** Permanent contract, continuous training, parking, flexible compensation (health insurance, transportation, childcare, training). * **On-site cafeteria:** Spacious facility with subsidized service. * **Location:** El Prat de Llobregat, well-connected by public transport (Bus 88, 110; Metro L10 ZAL–Riu Vell; PR4) and directly accessible via highway. **Discover why G+D is unique—check out this video:** ---------------------------------------------------------------- Giesecke+Devrient – We make the lives of billions of people more secure.**Privacy Notice** ------------------ The personal data you provide will be processed to manage your application in accordance with the GDPR and our Privacy Policy, available at Data Privacy | G+D.### ### **A look behind the scenes** ### **Contact** **HR Team Spain** seleccion.gdi@gi-de.com ### **JOB OFFER****Job Details** --------------- **Job Title** Data Processing Specialist **Business Sector** Giesecke + Devrient ePayments Iberia S.A C/ 114 nº 27 Polígon Pratenc **Requisition ID** 26339 **Location** Prat de Llobregat (BCN), ES **Career level** Experienced **Job Type** Full-time, Permanent contract **Contact** HR Team Spain seleccion.gdi@gi-de.com We are an equal opportunity employer. We promote diversity in all its forms and foster an inclusive workplace free from prejudice, discrimination, and harassment—where every employee feels valued and part of the community. We welcome all applications regardless of gender, age, race, ethnicity, socioeconomic or cultural background, religion, disability, or sexual orientation.

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

Negotiable Salary

Technical Mechanical Fitter647496964125461217

Technical Mechanical Fitter

Mechanic for machinery assembly and adjustment - Proven experience in machinery assembly. - Adjustment and assembly of each machine according to individual client specifications. - Interpretation of drawings and diagrams provided by the Technical Office. - Installation and assembly at the client’s premises. * 2 years’ experience. - Proven experience in machinery assembly. - Adjustment and assembly of each machine according to individual client specifications. - Interpretation of drawings and diagrams provided by the Technical Office. * Medium-level FP qualification * Catalan (intermediate spoken and written) * Spanish (intermediate spoken and written) * Driving licence: B * Permanent employment contract * Full-time position * Other relevant information: €22,000 per year + bonuses as per the Metalworkers’ Collective Agreement.

Carrer de la Creu Gran, 75, 08221 Terrassa, Barcelona, Spain

€ 22,000/year

Executive Medical Director, Hematology647496965404181218

Executive Medical Director, Hematology

**Executive Medical Director, Clinical Development, Hematology** **Location:** Boston, MA or Barcelona Spain **This is what you will do:** **General Description of the Role** The Executive Medical Director (EMD) role is generally assigned to be responsible for overseeing 2 or more programs, providing oversight/guidance/mentoring to the Medical Directors and Clinical Development Scientists on the teams, serving on cross\-asset strategic teams (e.g., disease strategy team) and providing input to strategic decisions at the TA Strategy Team and Global Medicine Team meetings Generally, the role may include managerial responsibilities over Senior Director, Medical Director Clinical Development directly and may support / oversee other Medical Directors/Clinical Development Scientists that report indirectly to the Executive Medical Director. The EMD may support development of regulatory strategy, therapeutic area and other functional strategies. **Specifics of the specialized role** The EMD is a specialized role and is specifically designated to provide medical leadership and input to Program Teams during the early to late stage of drug development (i.e., transitioning molecule through IND/CTA and First\-in\-Human study stage to Proof\-of\-Concept and End\-of\-Phase\-2 stage and beyond). The incumbent will serve as one of the medical experts for the study team(s) and may serve as the medical monitor for clinical trials as necessary. In line with its seniority, the EMD is typically responsible for multiple clinical development programs in a therapeutic area spanning IND to POC/Phase 2/3 under the supervision of a VP Clinical Development TA Head. In addition, she/he may also have responsibility for discrete, specific business development efforts (e.g., a due diligence on a specific target) and keep close ties with the Discovery and Research organizations. This position offers substantial opportunities for scientific and commercial interactions and career advancement in the fast\-moving area of rare disease. **You will be responsible for:** * Typically leading 2 program teams and drive the successful execution of clinical studies / programs / research strategies; define and manage the benefit to risk profile of our products * Representing Clinical Development on the Global Program Team (GPT) and Global Medicine Team in presentations at management and review committees (e.g., Clinical Document Review Committee, Development and Commercial Steering Committee); advance understanding of the impact our therapies have on the pathophysiology of rare and orphan diseases through scientific discourse and interpretation of data * Fostering development of Medical Directors and CDS and/or fellows. Lead and oversee 2 programs and the preparation and execution of a clinical development strategy and related documents including protocols, charters, statistical summary reports, meeting presentations, publications, and clinical sections of regulatory documents. * Providing scientific and medical input (consultative services) to other R\&D, commercial, translational, medicine and business development functions and leads and or oversees clinical activities to support due diligences * Representing Alexion Clinical Development to internal (R\&D management, cross functional development teams and executive committee) and external (academic, regulatory, and medical) communities. * Overseeing a cross functional team which develops the clinical components of the CDP. Serve as the Clinical input to Global Development Team / Subteams and medical expert for the clinical study team. Oversees the writing of the clinical sections of the CTD, white papers, expert opinion reports, and regulatory responses * Liaising internally with other members of the CDP to drive program strategy and CDPs. Coordinate communications and planning bet medical functions (Global Medical Affairs, Safety, Clinical Operations, Biostatistics, Epidemiology and Medical Science) as it relates to clinical development study design, execution and interpretation of results. Serves as the medical expert on the global product labeling team * Driving awareness of internal and external developments (scientific, clinical, competitive, and regulatory) that could impact the development plan, including attendance at major scientific conferences, participation in competitive intelligence activities, and periodic literature review * Writing or contribute to white papers, expert opinion reports, and regulatory responses * Driving clinical support of business development activities, such as due diligence and research collaborations * Critically evaluating available information about diseases of interest to the therapeutic area and the competitive landscape and synthesize information succinctly to support dissemination and incorporation into clinical development programs, asset plans and therapeutic area strategy * Determine appropriate advisory boards experts * Working as part of a cross\-functional team with colleagues representing, for example, biostatistics, data management, clinical pharmacology, commercial, regulatory and project management * May supervise other medical monitors on individual studies **You will need to have:** * Required: M.D. or equivalent * 7\+ years of experience in clinical development; clinical research, global regulatory, and product development expertise * Has prepared documents and attended regulatory meetings with FDA and other regulatory agencies * Experience designing and executing multinational clinical trials required * Demonstrated ability to lead cross\-functional teams to define clinical strategy and clinical study design * Experience supporting business development activities * MD or equivalent, preferably with clinical training * PhD in related discipline desirable, but not required * The duties of this role are generally conducted in an office environment. As is typical of an office\-based role, employees must be able, with or without an accommodation to: use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving and non\-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours **We would prefer for you to have:** * Preferred: Advanced knowledge of the assigned therapy area is desired, with the capability to interpret, discuss and represent trial or program level data. * 7\+ Years of experience in industry in clinical development is preferred

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

Negotiable Salary

AI Lab - Junior Machine Learning Engineer647324634914591219

AI Lab - Junior Machine Learning Engineer

**Junior Machine Learning Engineer (GenAI Modelling)** The AI Lab (under the well\-known Technology and Innovation Office) is responsible for bringing state\-of\-the\-art research in Generative AI (and AI in general) to HP’s product portfolio to solve top user needs and enable all new type of user experiences. The team will be in two main locations: Sant Cugat (ESP) and Palo Alto (US). The AI Lab goal is to operationalize the Gen AI model lifecycle, build models to support the top initiatives within Personal Systems, and do research on Generative AI. We are looking for a Junior Machine Learning Engineer with expertise and passion in the Gen AI space. The AI Lab is seeking an individual to join our team as an ML Engineer in our HP Sant Cugat R\&D unit. The candidate will research and develop generative AI models and work with other team members and business unit partners to develop proof\-of\-concept prototypes and help move technologies to product. Also, the candidate should be able to collaborate with other scientists, developers, and product managers on new applications. Strong communication skills are required. **Responsibilities**: * Help execute the technical strategy of the AI Lab with the goal of supporting HP ambitious AI roadmap. * Support the application of new processes and standards to ensure that the teams are building high quality and safe models. * Develop tooling to support the model lifecycle and encourages the use of best practices. * Adopts state\-of\-the\-art Gen AI modelling (finetuning) and evaluation techniques. * Help develop strategic engineering proof of concepts in the Gen AI space. **What are we looking for?** * BSc or MSc in Computer Science, Artificial Intelligence, Mathematics, Data Science, or any other related discipline or commensurate work experience or demonstrated competence. MSc related to Generative AI would be a plus. * Between 0 \- 3 years of work experience, internships related to the job content would also be valuable. Exposure to Gen AI in previous projects / internships. * Good communication and interpersonal skills, with the ability to collaborate effectively and learning with agility. **Knowledge \& Skills**: * Programming Language/s certification (Python, and C\+\+ / C\# is a plus). * Knowledge of machine learning, deep learning, generative AI and statistical modelling. * Finetuning or evaluation work pursued in generative AI and machine learning (LLMs, LVMs) development and deployment. * Experience leveraging models from repositories such as Hugging Face. * Experience with deep learning frameworks such as PyTorch. * Optional: Contributions to the AI community (e.g., publications, patents, open\-source projects, or participation in conferences and workshops). **What we offer:** * Opportunity to work in an international organization with colleagues coming from all over the world. * Diverse, continued internal growth and career opportunities. Including HP’s own learning platform and LinkedIn Learning. * An attractive benefits package: + Health \& Life insurance. + Lunch at reduced prices at our canteen/ ticket restaurant vouchers. + HP product discount. * Work life balance / flexible working hours. * Women, Pride, Young employees, Sustainability and DisAbility! Just a few of our fantastic global business networks you can get involved with locally. * We also dedicate time and resources to contribute with our community through Corporate Volunteering activities, including our onsite HP Charity day. * Do you like to give back to the community? Then join one of our many volunteering teams or be a part of the incredible HP charity day held on site annually. * Love sports? Then take advantage of our sports center (indoor and outdoor) with 25\+ regular coordinated activities. * We have an onsite Doctor and medical team for our employees, including services such as: nutrition, physiotherapy, and general health. * Printing Happy hour – from photographs to large posters. And Hands\-on workshops to print with the latest technology – from wall covers to 3D printed models. * Our Women Network organizes activities such as Networking, the promotion of STEM vocations, talks on, improving business acumen, work life balance and skills of the future, etc. 6763

Carrer d'Elisenda Ribatallada, 11, 08172 Sant Cugat del Vallès, Barcelona, Spain

Negotiable Salary

ESTHETICIAN647324636482571220

We need to hire an experienced esthetician for a center located in the upper area of Barcelona. Experience in apparatus-based treatments, manicures, facial and body treatments is mandatory. Responsibilities include performing facial and body treatments, apparatus-based treatments, manicures, and pedicures. Minimum 2 years of experience. Experience in apparatus-based treatments, manicures, facial and body treatments is mandatory. * Indefinite-term employment contract * Intensive work schedule

Carrer dels Madrazo, 48, Sarrià-Sant Gervasi, 08006 Barcelona, Spain

Negotiable Salary

PHYSICAL ACTIVITY INSTRUCTOR – RUBÍ647324634762251221

PHYSICAL ACTIVITY INSTRUCTOR – RUBÍ

We are looking for a Physical Activity Instructor for seniors in Rubí. Two sessions per week: Wednesdays from 17:15 to 18:15 and Fridays from 11:00 to 12:00. Start date: 14/01 until the end of the academic term. Lead physical activity workshops for seniors. * Minimum 1 year of experience. Experience in workshops and facilitation of leisure and sociocultural activities. * Competencies / knowledge: Social skills * Temporary employment contract (7 months) * Part-time schedule (5 hours \- weekly workload) * Gross monthly salary ranging from '100' to '120'

Carrer de Monturiol, 72, 08191 Rubí, Barcelona, Spain

€ 100-120/day

Kitchen Staff (ASL) - Barcelona647324630851851222

Kitchen Staff (ASL) - Barcelona

Compass Group España is part of Compass Group PLC, the global leader in Foodservice and Support Services. For over 50 years, we have provided our services across key sectors including Business & Industry, Healthcare, Seniors, Education, Sports & Leisure, and Catering, with a portfolio of market-recognized brands. We rank among the world’s top 10 employers, with a team of 600,000 people across 50 countries, serving approximately 4 billion meals annually and working daily with 40,000 clients. Throughout these years, our team has consistently upheld its commitment to our clients, the quality of our service, and our spirit of innovation. The Compass success formula: experience, trust, commitment, and the best team of professionals. If you wish to share our vision, join this outstanding team. Eurest Colectividades S.L. guarantees equal opportunities and fair evaluation of all applications submitted for this selection process. Functions - Kitchen and pantry cleaning * Cold and hot food plating. * Dishwashing line * Waste disposal Requirements - Residence in the Sarrià-Sant Gervasi area – Barcelona * Experience working as ASL (Auxiliary Service Worker) in collective catering and/or restaurant kitchens Offer Temporary contract to cover holidays from December 29 to January 12 Full-time position Working hours: Monday to Friday, 3:00 PM to 11:00 PM Salary: Collective Agreement for Collective Catering – €883.13 gross per month, paid in 14 installments

Carrer de Pomaret, 98I, Sarrià-Sant Gervasi, 08017 Barcelona, Spain

INDUSTRIAL MAINTENANCE MECHANIC647063254083851223

INDUSTRIAL MAINTENANCE MECHANIC

We are a plastic injection and thermoforming company located in Castellbisbal, and we are seeking a trainee to carry out internships at our company. The start date would be January 7th, on a part-time basis, with the possibility of permanent integration into our staff. Below are the tasks to be performed: * Industrial/hydraulic maintenance: Carry out preventive and corrective maintenance tasks on equipment, ensuring their proper operation. * Diagnose and repair mechanical failures in production equipment. * Adjust, assemble, and disassemble mechanical components. * Participate in continuous improvement projects and optimization of production processes. * Coordinate with electrical and production teams to ensure operational efficiency. * Completion of documentation Technical training in the field of industrial maintenance, as well as the ability to work effectively in a team and solve problems efficiently, will be highly valued. This is an ideal opportunity to develop skills and gain practical experience in a dynamic and constantly evolving industrial environment.

Carrer de l´Esperanto, 12, 08755 Castellbisbal, Barcelona, Spain

Negotiable Salary

Waiter/Waitress647062349934101224

Waiter/Waitress

We are looking for a waiter/waitress passionate about the hospitality industry and with experience in customer service. If you are a dynamic person with exceptional tray-handling skills and teamwork abilities, apply to our offer. **Requirements:** * Minimum three years’ experience in the position * Proficiency in Catalan and Spanish * Availability to work split shifts * Availability to start from 20/08 * Food handling certification is an advantage **We offer:** * Permanent full-time contract * Salary: €21,631 gross annual base salary + variable components * Working hours: full-time * Excellent working environment where collaboration and camaraderie are fundamental * Opportunities for promotion within our organization

Carrer d'Elisenda Ribatallada, 11, 08172 Sant Cugat del Vallès, Barcelona, Spain

€ 21,631/year

SAP SucessFactors (EC LMS) Consultant | Lisbon647062348776981225

SAP SucessFactors (EC LMS) Consultant | Lisbon

VNG \- Cais de Gaia, Lisboa \- Colombo SAP SucessFactors (EC LMS) Consultant \| Lisbon SAP SucessFactors Consultant 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 Senior SAP SuccessFactors Employee Central Consultant to join our teams in Lisbon. In this role you will be responsible for: * Resolving challenging functional and technical issues with strong focus on SAP SF Employee Central; * Collaborate with business to understand and document opportunities and existing problems; * Resolve functional problems, escalate and track problems appropriately; * Manage system configuration in accordance with corporate guidelines and policies; * Create and deliver appropriate documentation, training and communication around feature(s) and process changes; * Participate in the design of new enhancements and business processes that will improve operational efficiency across the organization; * Create and deliver appropriate documentation, training and communication around feature(s) and process changes. YOUR PROFILE* Degree in Computer Science or similar; * \+3 Years' of Experience in implementation of SAP SuccessFactors Employee Central Module; * At least 2 SAP SF EC implementations; * Experience in Time off and/ or Time\-sheet is a plus; * SAP SF Employee Central Certification; * Knowledge in Payroll (PY) will be a plus; * Nice to have: Organizational Management (OM) and Personnel Administration (PA); * Fluency in English (written and oral). WHAT YOU’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 fueled 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 \#LI\-Hybrid Ref. code 214129\-en\_GB Posted on 15 Apr 2025 Experience level Experienced Professionals Contract type Permanent Location VNG \- Cais de Gaia, Lisboa \- Colombo Business unit ABL Southern Central Europe Brand Capgemini Professional communities SaaS Solutions

WWG6+35 Gaià, Spain

Negotiable Salary

Site Manager for Metal Structures and Industrial Locksmithing646949336057611226

Site Manager for Metal Structures and Industrial Locksmithing

Tallers Vidal Amill is a company located in Anglesola, specializing in the **manufacturing and assembly of metal structures and industrial locksmithing**. We are currently seeking an experienced **Site Manager** with expertise in metalwork and a strategic vision to coordinate workshop and on-site projects. Key responsibilities include: \- Managing and planning construction sites involving our manufacturing output. \- Coordinating the **day-to-day activities of assembly teams**. \- **Taking measurements and technical details**, then communicating them to the **technical office and workshop**. \- Ensuring **quality, deadlines, costs, and certifications** for each project. \- **Proposing improvements, solutions, and possible technical modifications** to clients or site management. \- Collaborating with **Management, Technical Office, and Workshop** to ensure efficient execution. This opportunity may interest you if you meet the following requirements: \- Prior experience in **metal structures or industrial locksmithing**. \- Knowledge of **technical drawings, assembly processes, and manufacturing procedures**. \- Strong organizational, leadership, and team management skills. \- A **solution-oriented, proactive individual** with both technical and economic insight into projects. \- Excellent communication skills and direct interaction capability with clients and site management. \- Willingness to work within the **province of Barcelona**. We offer: \- Attractive employment and remuneration conditions (to be discussed based on qualifications and experience). \- Company vehicle and mobile phone. \- Diverse projects and managerial autonomy. \- A positive working environment. Job type: Full-time, Permanent contract Salary: €35,000.00–€45,000.00 per year Benefits: * Meals provided at the company * Company events * Flexible working hours * Option for a permanent contract * Private health insurance * Company mobile phone Work location: On-site employment

Avinguda del Mestre Montaner, 103, 08700 Igualada, Barcelona, Spain

€ 35,000-45,000/year

LILA POINT AGENT646949335258901227

LILA POINT AGENT

Doble Via is looking for you! If you are a proactive, dynamic, enthusiastic person who loves teamwork and feels passionate about supporting others, send us your CV. We want you to join our great team! With 25 years of history, we provide comprehensive services for the management of facilities and programs in social and cultural action, education, sociocultural animation, and community development, as well as advisory and support services for designing and planning initiatives in these fields across all life stages—from childhood to old age. You will have the opportunity to work, train, and grow professionally within a dynamic environment. We are a cooperative that places people at the core and are committed to equal opportunities and gender equality. We are seeking Lila Point Agents for New Year’s Eve. During this period, we deploy Lila Points in various municipalities. Lila Points are information and awareness-raising spaces focused on male violence and LGBTIQ+-phobic violence, open to the general public. Additionally, they serve as safe spaces offering advice and accompaniment to anyone experiencing or witnessing male or LGBTIQ+-phobic aggression during nighttime leisure activities, in accordance with the municipal protocol agreed upon by all agencies involved in the event. Municipalities where we operate Lila Points: - Maresme - Baix Llobregat - Vallès Oriental - Vallès Occidental What are we looking for? - Empathetic individuals capable of conducting interventions based on active listening and emotional support, avoiding victim-blaming and re-victimization. - Diplomatic individuals, non-judgmental, and able to follow the pace set by the person being assisted. - Organizational skills, proactivity, and versatility. - Problem-solving ability and capacity for teamwork. - Flexibility regarding working hours. - Immediate availability to start. - High-level Catalan proficiency. - Minimum one year of prior experience (volunteer experience is valued). - Training in male violence, gender issues, sexual violence, or LGBTI-phobia. * Temporary employment contract (6 months) * Flexible working hours

Carrer de Menéndez y Pelayo, 1S, Les Corts, 08028 Barcelona, Spain

Negotiable Salary

Reservation Trainee646948512389151228

Reservation Trainee

**Additional Information** **Job Number**25196999 **Job Category**Management Development Programs/Interns **Location**Le Meridien Barcelona, La Rambla 111, Barcelona, Barcelona, Spain, 8001 **Schedule**Full Time **Located Remotely?**N **Position Type** Non\-Management Build upon your classroom studies through our Hotel Internship Program opportunities. You will learn first\-hand about a hotel's operations. Our Hotel Internship Program allows you to truly experience the industry from the ground up, where our founders and many of our leaders began. You will get immersed in Marriott's culture and business and find your true calling in the travel industry. Our internships are typically available in many different areas of the hotel. By gaining hands\-on experience in the exciting world of hotel management, you�ll be better prepared to pursue opportunities post graduation. Here�s to exploring, kickstarting your dream career, and joining us on your journey! To be considered for an internship, you must be a current college or university student. Want to join us? Apply now! Marriott International is the world�s largest hotel company, with more brands, more hotels and more opportunities for associates to grow and succeed. We believe a great career is a journey of discovery and exploration. So, we ask, where will your journey take you? marriotthotelinternship *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

Negotiable Salary

Installation Technician646847675225611229

Installation Technician

Grup Carles is collaborating with an installation company based in Igualada to incorporate an Installation Technician into its team. Reporting to the Service Manager, the candidate will be responsible for carrying out installation tasks for new construction and industrial, commercial, and residential renovation projects. Electrical, HVAC, water, and gas installations... We offer: - The opportunity to join a highly established company with a family-oriented work environment. - Participation in projects located in the Anoia region. - Immediate full-time incorporation. - Professional stability. - Salary negotiable per candidate. Requirements: * Minimum experience as an electrician and in electrical, HVAC, water, and gas installations. * Geographic proximity to the workplace. 3 years of experience. Experience in electrical installations, plumbing, gas... * Permanent employment contract * Full-time position * Additional relevant information: Hiring through the company or as a self-employed professional.

Avinguda del Mestre Montaner, 103, 08700 Igualada, Barcelona, Spain

Negotiable Salary

Previous
1(current)
2
3
4
Next

Popular Jobs

Popular Cities

Manufacturing， Transport & Logistics Recruitment Other Recruitment Community Services & Development Recruitment Purchasing， Procurement & Inventory Recruitment

Extremadura Freight/Cargo Forwarding Recruitment Sant Joan Freight/Cargo Forwarding Recruitment Basque Country Freight/Cargo Forwarding Recruitment Camargo Freight/Cargo Forwarding Recruitment Rota Freight/Cargo Forwarding Recruitment sa Pobla Freight/Cargo Forwarding Recruitment Santander Freight/Cargo Forwarding Recruitment Cantabria Freight/Cargo Forwarding Recruitment Canary Islands Freight/Cargo Forwarding Recruitment Canet de Mar Freight/Cargo Forwarding Recruitment

Help

Support and feedback

Cookie

Cookie Settings

Our Apps

Download on the

APP Store

Download

Get it on

Google Play

© 2025 Servanan International Pte. Ltd.