Donostia / San Sebastian Testing & Quality Assurance Job Listings

Indeed

QA Tester

At ORBIK, we are looking to hire a QA Tester who will join our technical team to collaborate on innovative projects, ensuring the quality and reliability of our backend and frontend applications. **Responsibilities:** * Define, design, and execute test plans for applications. * Automate integration and functional tests using modern frameworks. * Document and manage issues detected during testing. * Collaborate closely with development, product, and DevOps teams. * Contribute to the continuous improvement of QA processes and tools. **Requirements:** * Previous experience as a QA Tester. * Knowledge of automated testing tools such as Selenium, Playwright, or Cypress. * Strong analytical skills and attention to detail. * Good communication and teamwork abilities. **Nice to have:** * Experience with CI/CD and integration of tests into pipelines. * Knowledge of Docker and Kubernetes for testing in modern environments. * Familiarity with programming languages such as Golang and React. **Benefits:** * Competitive salary and comprehensive benefits package * Opportunities for professional growth and advancement * Work with cutting\-edge technologies in a collaborative environment * Flexible work arrangements to support work\-life balance

Garibai Hiribidea, 2, 20500 Arrasate / Mondragón, Gipuzkoa, Spain

Negotiable Salary

Senior Validation Technician64617014306306121

Indeed

Senior Validation Technician

**About us** ------------------ We are an industrial company **leading internationally in the field of biotechnology and advanced therapies, based in Donostia\-San Sebastián, with a major expansion project, an unwavering passion for science, and a commitment to excellence and people.** Our **purpose:** improving people's lives through revolutionary advances in biotechnology and gene therapy that cure rare diseases and cancers. With a philosophy of not only working together but growing together, our client's culture is based on honesty, excellence, leadership, engagement, ethics, and rigor. We are a **CDMO** (Contract Development and Manufacturing Organization), and **the trust placed in us by more than 40 biotech companies worldwide is our best endorsement.** We develop and manufacture viral vectors (lentiviral), being one of the European leaders operating in accordance with EMA and FDA regulations. Lentiviruses produced by VIVEbiotech are used for treating various diseases including hematological and solid cancers, or rare diseases. **We are looking for you to join our Team!** ### **Your role** We are seeking a **Senior Validation Technician**, reporting to the Head of Quality Assurance – Manufacturing. **Your mission will be to ensure the integrity and compliance of validation activities according to GMP regulations and VIVEbiotech's internal standards.** Likewise, you will **collaborate with the Operations team to evaluate process changes and deviations that could impact compliance with the validation status**, designing necessary actions to ensure maintenance and proper validation status. ### **Your responsibilities** * You will contribute to the design and implementation of validation projects strategy. * You will review and approve validations according to the defined strategy and established validation plans. Likewise, you will review and approve validation protocols, final reports, and raw data supporting the information contained therein. * You will coordinate with different departments the execution of validation protocols. * You will apply Risk Management throughout each validation stage. * You will report significant activities and incidents to your direct supervisor and Operations managers, proposing solutions contributing to continuous improvement in validation management. * You will also collaborate with Operations teams to assess process changes and deviations that may impact compliance with validation status, designing necessary actions to ensure maintenance and correct validation status. * You will coordinate the management of incidents and deviations arising during validations, ensuring they are handled and closed in accordance with the Quality System. * You will review deviations and change controls associated with processes, evaluating their impact on validation status through appropriate Risk Assessments and proposing strategies to ensure compliance. * You will propose strategies for improvement and optimization of production processes, for which you must have an in-depth understanding of VIVEbiotech's lentiviral vector production process. * You will establish internal links with adjacent departments within the company to ensure smooth project progress. * Similarly, whenever required by the department, you will provide support to the Manufacturing QA area in managing the Quality Management System: * You will collaborate with your direct supervisor in developing and implementing the annual management plan for your area of responsibility, always with a cost-effectiveness continuous improvement vision impacting overall company enhancement. * You will report significant activities and incidents to your direct supervisor, proposing solutions driving continuous improvement in your area. * You will take on a leadership role in promoting VIVE culture both within and outside your team: behavioral values and teamwork, customer orientation, and continuous improvement in quality, safety, and environment. ### **What we value in you** **We are looking for someone with:** * Degree in Pharmacy, Biotechnology, Biology, Biochemistry, or related fields, complemented with knowledge in Regulatory Compliance (GMP, etc.). * Experience in Process Validation. * Expert knowledge of Good Manufacturing Practices (GMP) according to EMA and FDA standards. * Previous experience in the pharmaceutical industry in similar roles, with GMP certification. * Experience in the pharmaceutical industry in similar roles with GMP Part IV certification (GMP Guidelines specific to Advanced Therapy Medicinal Products), Annex I Sterile Medicinal Products Manufacture, and experience in environments regulated under FDA requirements. * Experience in root cause analysis and risk management. * Experience using computerized systems applied to the pharmaceutical industry. * Quality orientation, with a strong sense of excellence and self-discipline, working in an organized and methodical manner. * Proactive contribution with continuous improvement ideas, offering your knowledge and experience to help achieve departmental goals. * Ability to work effectively, proactively, and collaboratively within a team. * Responsibility and meticulousness in work, maintaining high performance under demanding results and deadlines. * Consistently positive attitude towards change. * Residing in Gipuzkoa or willingness to relocate to the area will be positively valued. ### **We offer you** * You will have continuous career development opportunities that will help you grow your talent throughout your professional journey. * You will participate in innovative projects undergoing constant technological updates. * You will receive a competitive salary commensurate with your profile for this position. * You will benefit from flexible working hours, with the support needed to balance your personal and professional life. * You will become part of an expert, young, dynamic, innovative, and enthusiastic team united by a common purpose: supporting our clients in advancing cures for diseases. * We will support your personal relocation process if you come from another region and wish to move to Donostia\-San Sebastián (accommodation, job placement for family members, school enrollment, etc.). * You will enjoy a professional work environment truly distinguished by our humanity and closeness, where we care about diversity and inclusion. Diverse perspectives and your curiosity bring varied capabilities that strengthen our approach and drive our growth. * We are proud to offer equal opportunities. All individuals receive equal consideration for our open positions, without regard to gender, age, race, religion, identity, sexual orientation, origin, disability, or any other characteristic.

Cristina-Enea Parkea, 3, 20012 Donostia / San Sebastián, Gipuzkoa, Spain

Negotiable Salary

part time Analyst-Revenue64550873979010122

Indeed

part time Analyst-Revenue

**Additional Information** **Job Number**25190716 **Job Category**Revenue Management **Location**Hotel Maria Cristina a Luxury Collection Hotel San Sebastian, Paseo Republica Argentina, 4, San Sebastian, Guipuzcoa, Spain, 20004 **Schedule**Part Time **Located Remotely?**N **Position Type** Non\-Management **POSITION SUMMARY** Assist in the management of rooms inventory to maximize rooms revenue, as well as maintain accuracy of information and enhance automation efforts in reservation system. Assist in the preparation of competitive analysis and other supporting documents for presentation at market sales strategy meetings. Assist in managing room authorizations, rates, and restrictions, including communicating rate restrictions and strategy to properties. Perform all Revenue Management daily and weekly reporting, month end reporting and auditing and provide forward looking information for the purposes of forecasting, targeting need areas and balancing financial expectations. Accurately generate, process and update all property and market Revenue Management reports and serve as primary source for majority of reporting and analytical needs of the Revenue Management team. Assist with system maintenance including but not limited to, inputting rate hurdles, monitoring forecasted demand, updating group forecasting and running daily system checks. Assist with training of new associates as necessary on revenue management tools. Assist in the implementation of hotel sales strategies in the reservation and inventory systems. Follow all company policies and procedures; ensure uniform and personal appearances are clean and professional; maintain confidentiality of proprietary information; protect company assets. Welcome and acknowledge all guests according to company standards; anticipate and address guests’ service needs; thank guests with genuine appreciation. Speak with others using clear and professional language; answer telephones using appropriate etiquette. Develop and maintain positive working relationships with others; listen and respond appropriately to the concerns of other employees. Comply with quality assurance expectations and standards. Read and visually verify information in a variety of formats; move, lift, carry, push, pull, and place objects weighing less than or equal to 15 pounds without assistance; stand, sit, or walk for an extended period of time. Perform other reasonable job duties as requested. PREFERRED QUALIFICATIONS Education: High School diploma or G.E.D. equivalent. Related Work Experience: At least 1 year related work experience. Supervisory Experience: No supervisory experience. License or Certification: None *At Marriott International, we are dedicated to being an equal opportunity employer, welcoming all and providing access to opportunity. We actively foster an environment where the unique backgrounds of our associates are valued and celebrated. Our greatest strength lies in the rich blend of culture, talent, and experiences of our associates. We are committed to non\-discrimination on any protected basis, including disability, veteran status, or other basis protected by applicable law.* *At 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.* The Luxury Collection Hotels \& Resorts, with over 120 properties in more than 35 countries, offers the promise of authentic experiences that evoke lasting, treasured memories. Our more than 100 years of experience, beginning in 1906 under the Italian CIGA brand – a collection of Europe's most celebrated and iconic properties – serves as a solid foundation as we continuously evolve to exceed the desires of the luxury traveler. From legendary palaces and remote retreats to timeless modern classics, each luxury hotel and resort is a unique and cherished expression of its locale – a portal to the destination’s cultural charms and treasures. If you are someone with an appreciation for evocative storytelling, a keen interest and passion for this destination's heritage, and a desire to deliver genuine, personalized, and anticipatory hospitality, then we invite you on our journey. In joining The Luxury Collection, 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.

República Argentina K., 14, 20002 Donostia / San Sebastián, Gipuzkoa, Spain

Negotiable Salary

IT Deployment Engineer (LIMS)64522512161793123

Indeed

IT Deployment Engineer (LIMS)

**Company Description** Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. **Job Description** As an **IT Deployment Engineer LIMS**, you will provide 1st and 2nd Line Support for our European network of clinical diagnostics laboratories with a focus on the core Laboratory Information Management System. **Key Responsibilities:** * Register, classify, route, follow\-up and resolve request via e\-mail or ticketing system. * Become an expert in the LIMS Application and functionality and provide training to end users face to face or on site * Attend on site deployments to configure LIMS processes alongside laboratory staff * Work alongside development teams to balance development and configuration * Diagnose and troubleshoot Application, hardware or Cloud infrastructure problems, researching and answering questions. * Maintain accurate records of all support interactions in Eurofins IT Service Management Tool (ServiceNow, BMC Helix). * Own the incoming requests and manages escalations to engineering or development teams with clear documentation. * Monitor system performance and generate reports to anticipate or detect issues. * Contribute to technical documentation, FAQs, and knowledge base articles. * Work collaboratively with cross\-functional teams including QA, DevOps, and Product to improve the customer experience. * Execute, participate and report on IT \& Application project rollout **Qualifications** **Experience \& Qualifications** * Bachelor’s degree in computer science, Information Technology, Engineering, or equivalent experience. * Any Prior LIMS experience is an advantage but not necessary * Proven experience in technical support, IT or system engineering role. * Experience in application troubleshooting * Experience in troubleshooting Windows 10, 11, networking fundamentals and cloud platforms (AWS, etc.) * Experience of Oracle RDBMS and Linux OS * Experience with monitoring tools, ticketing systems, and diagnostic utilities. * Excellent communication and interpersonal skills. * Very good command of English written and spoken. * Can do approach, and capability to work in dynamically changing environment. * Some travel 25% **Additional Information** **We support your development!** Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development. **We embrace diversity!** As an Equal Opportunity Employer, the Eurofins network of companies believes in strength and innovation through diversity. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. **Sustainability matters to us!** We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we count on our dedicated carbon reduction team to help us to achieve this goal! Find out more on our Careers page: https://careers.eurofins.com/ **Company description:** Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies believes that it is a global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in\-vitro diagnostic products. In over 37 years, Eurofins has grown from one laboratory in Nantes, France to over 65,000 staff across a decentralised and entrepreneurial network of more than 950 laboratories in over 1,000 companies across 60 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2024, Eurofins generated total revenues of EUR 6\.95 billion, and has been among the best performing stocks in Europe over the past 20 years.

Cristina-Enea Parkea, 3, 20012 Donostia / San Sebastián, Gipuzkoa, Spain

Negotiable Salary

QA Operations Technician64521252240386124

Indeed

QA Operations Technician

**About the role** We are seeking a motivated **QA Technician** to join our Quality Assurance Operations team. In this role, you will be responsible for ensuring compliance with GMP and ensure that our manufacturing process meet the required quality standards and regulatory requirements. You will play a crucial role in maintaining compliance with industry regulations and ensuring that our products are safe and effective. **Key Tasks:** * Implement and effectively maintain the quality management system. * Ensure compliance with applicable GMP regulatory standards and guidelines. * Revision of manufacturing batch records and quality control records of GMP batches required for product certification/confirmation * Manage the document control system ensuring the accuracy completeness and accessibility of quality related documents. * Assist in the review, preparation and maintenance of all quality\-related documents, including protocols, reports, SOPs, batch records, specifications… * Identify issues found during the review of batch documentation. * Management of complaints, quality events and change control. * Collaborate with internal teams to implement CAPAs resulting from audits, inspections, and quality assessments. * Track and monitor the effectiveness of CAPAs. * Attend the technical teams in the daily event of quality with the support of Quality Assurance team. * Assist in the development and implementation of training programs related to GMP. * Participate in the continuous improvement. * Ensure the effective communication and escalation process of quality issues to appropriate management levels. * Provide support in project activities * Support training initiatives for internal staff on GMP compliance and quality assurance practices. * Stay updated on industry regulations and best practices regarding for GMP compliance. **Skills \& Qualifications:** * Bachelor’s degree in a Science field (e.g., Pharmacy, Biology, Chemistry, Biotechnology). * Minimum of 2 years of experience in quality or production roles. * Knowledge of quality control methodologies and regulatory requirements. * Strong attention to detail and analytical skills. * Excellent communication and interpersonal skills, with the ability to work collaboratively across teams. * Adaptability in using quality management software and tools. * Ability to work in a fast\-paced environment and manage multiple tasks effectively. * Company values: Humility, Empathy, Responsibility, Commitment, Teamwork, and Effort. **We Offer:** * A dynamic and collaborative work environment. * Opportunities for professional development and continuous training. * Direct impact on the development of therapies that improve people's lives. * Additional benefits; health insurance, vacation, flexibility, etc. If you are ready to take your career to the next level and make a difference in the world of biotechnology, we would like to meet you!

Pagola Kalea, 7, 20018 Donostia / San Sebastián, Gipuzkoa, Spain

Negotiable Salary

Senior QA Automation Engineer64145142062339125

Indeed

Senior QA Automation Engineer

Are you a forward\-thinking professional with a strong background in QA Automation and an interest in financial services? Join EPAM in Madrid as a **QA Automation Engineer** in the private banking sector and accelerate your career in financial services technology. We are seeking a collaborative team player with exceptional communication skills, advanced engineering expertise and full proficiency in English for effective stakeholder interactions. This is a hybrid role based in Madrid's city center, ideal for those eager to thrive in a dynamic environment and make a significant impact in private banking technology. **Work flexibly from anywhere in Spain, with three days a week in our Madrid office to collaborate closely with the team.** Join EPAM and contribute to shaping the future of financial services in Spain! **Responsibilities** * Oversee and manage all aspects related to software quality within the team * Identify tests for test automation * Identify, prioritize and automate regression and critical path test scenarios using Selenium WebDriver with Java or C\# and Tricentis Tosca (Commander, Engine, Analytics) * Perform manual testing as needed, including periods where manual testing may be the primary responsibility * Create or organize required Test data * Maintain (add, remove, update) regression test cases * Execute and document the execution of tests in an audit proved manner * Read and write code in Java or C\# when required * Manage and oversee the identification, tracking and resolution of defects to ensure optimal software performance and quality **Requirements** * 5\+ years general Test Automation experience covering UI and API * Strong experience with Tricentis Tosca * BSc/MSc in Computer Science, Engineering or related field * Work experience in an agile team is mandatory, in a DevOps setup is a strong plus * Strong experience in Test case design (TCD) to ensure proper coverage of requirements/acceptance criteria * Experience in risk\-based testing * Capable of performing manual testing when necessary * Self\-guided exploration of DB to find relevant test data * Good Jira knowledge * Great communication skills in English * Fluent Spanish would be a big plus **Nice to have** * Experience working with cloud technologies * Familiarity with web application architecture * Knowledge of the banking domain, particularly in Client Lifecycle Management * Basic XRAY knowledge **We offer** * Private health insurance * EPAM Employees Stock Purchase Plan * 100% paid sick leave * Referral Program * Professional certification * Language courses EPAM is a leading digital transformation services and product engineering company with 61,700\+ EPAMers in 55\+ countries and regions. Since 1993, our multidisciplinary teams have been helping make the future real for our clients and communities around the world. In 2018, we opened an office in Spain that quickly grew to over 1,450 EPAMers distributed between the offices in Málaga, Madrid and Cáceres as well as remotely across the country. Here you will collaborate with multinational teams, contribute to numerous innovative projects, and have an opportunity to learn and grow continuously. * **Why Join EPAM** * **WORK AND LIFE BALANCE.** Enjoy more of your personal time with flexible work options, 24 working days of annual leave and paid time off for numerous public holidays. * **CONTINUOUS LEARNING CULTURE.** Craft your personal Career Development Plan to align with your learning objectives. Take advantage of internal training, mentorship, sponsored certifications and LinkedIn courses. * **CLEAR AND DIFFERENT CAREER PATHS.** Grow in engineering or managerial direction to become a People Manager, in\-depth technical specialist, Solution Architect, or Project/Delivery Manager. * **STRONG PROFESSIONAL COMMUNITY.** Join a global EPAM community of highly skilled experts and connect with them to solve challenges, exchange ideas, share expertise and make friends.

Cristina-Enea Parkea, 3, 20012 Donostia, Gipuzkoa, Spain

Negotiable Salary

Indeed

Project Manager

Are you interested in growing as a professional, actively participating in project decisions, and doing so alongside an experienced team in a close and collaborative work environment? **This is your opportunity!** If you want to work towards a more sustainable and responsible world, at CAF Digital Services we believe in and work on sustainable mobility, one of the main challenges facing today's society. At CAF Digital Services, we improve train availability and passenger well-being through data analytics and digitalization. We work with the most innovative maintenance and operation technologies to maximize train service quality. **What do we offer you?** **Positive Work Environment:** You will become part of a highly qualified team surrounded by people with a strong collaborative spirit, where you will find a close and pleasant atmosphere. **Work-Life Balance:** Our hybrid model will allow you to perfectly balance your family and professional life. **Learning and Autonomy:** We will encourage you to work autonomously, supported by our training programs, with a highly technological product and within an international market. **Security and Stability:** CAF has been working for over 100 years on a path extending into the future, providing you with the security you need. **What will make you succeed in this position?** * Bachelor’s or Master’s degree in Engineering. * Strong comprehension and communication skills in English. * Good project and service management capabilities. * Proactive attitude and ability to work in a team. * Knowledge of a second language is valued positively. **What will be your mission in the company?** Your mission will be managing international projects and services within the railway sector (projects involving the design and implementation of software applications and hardware systems). **Position Responsibilities:** * Planning * Specification, negotiation, monitoring, and fulfillment of requirements. * Risk management * Technical presentation and negotiation with clients * Monitoring and coordination of subcontracting related to projects and client needs * Supporting resolution of incidents during the warranty phase of developments * Client training * Client follow-up to introduce new developments Therefore, if you are interested in working at a digital company striving for a more sustainable and responsible world, committed to equal opportunities and with an Equality Plan, do not hesitate—apply for the position now.

Cristina-Enea Parkea, 3, 20012 Donostia, Gipuzkoa, Spain

Negotiable Salary

Operational Quality Technician64145124783233127

Indeed

Operational Quality Technician

**About us** ------------------ We are an industrial company **leading internationally in the field of biotechnology and advanced therapies, based in Donostia\-San Sebastián, with a major expansion project, an unwavering passion for science, and a commitment to excellence and people.** Our **purpose:** improving people's lives through revolutionary advances in biotechnology and gene therapy that cure rare diseases and cancers. With a philosophy of not only working together but growing together, our client's culture is built on honesty, excellence, leadership, engagement, ethics, and rigor. We are a **CDMO** (Contract Development and Manufacturing Organization) and **the trust placed in us by more than 40 biotech companies worldwide is our best endorsement.** We develop and manufacture viral vectors (lentiviral), being one of the European leaders operating in accordance with EMA and FDA regulations. Lentiviruses produced by VIVEbiotech are used for treating various diseases including hematological and solid cancers, or rare diseases. **We are looking for you to join our Team!** ### **Your role** We are seeking an **Operational Quality Technician (GMP)** to fill this key position reporting directly to the GMP Team Leader. Your **mission** will be to keep the **GMP documentation of the Production Area continuously up to date.** Similarly, you will **participate in investigating incidents during the manufacturing process and propose corrective and/or improvement actions** for processes in cooperation with the Production team and the Quality Assurance Department. ### **Your responsibilities** * Keep current all GMP documentation of the Production area derived from the company's Quality Management System. * Receive GMP batch deviations and incidents from different types of batches to carry out the relevant investigations. * Conduct self-inspections in the Production Area, preparing status reports and improvement proposals. * Stay constantly and proactively updated regarding changes in existing production processes within the company. * Prepare change controls for the section, whether arising from incidents or continuous improvement, and coordinate internally (if cross-departmental). * Proactively participate in the investigation of manufacturing incidents, proposing corrective and/or improvement actions for processes, in cooperation with the Production team and the Quality Assurance Department. * Draft and update required SOPs for the section, and inform/train personnel on SOP changes to schedule corresponding training sessions. * Participate in the preparation of External Audits when necessary. * Coordinate with the Quality Assurance Department to implement new quality policies in the section. ### **What we value in you** You are who we are looking for if: * You have studies related to Biotechnology, Biology, Pharmacy, etc., complemented with knowledge of Regulatory Compliance (GMP, etc.) * You have at least one year of experience in the main functions described, either in Quality Assurance or Production departments. * You are a person oriented toward high quality (excellence and self-demand), organized and detail-oriented. * You proactively provide ideas for continuous improvement and share your knowledge and experience to help achieve your section's objectives. * You have the ability to work effectively within a team and are proactive. * You are responsible and rigorous in your work, demonstrating strong work capacity under high performance demands and tight deadlines. * You consistently show a positive attitude toward change. * Residency in Gipuzkoa (or intention to relocate to the area) will be positively valued. ### **What we offer** * You will have access to continuous career development that will help you grow your talent throughout your professional journey. * You will participate in innovative projects with constant technological updates. * You will receive a competitive salary aligned with your profile for this position. * You will benefit from flexible working hours, with the support needed to balance your personal and professional life. * You will become part of an expert, young, dynamic, innovative, and enthusiastic team united by a common purpose: supporting our clients in advancing cures for diseases. * We will support your personal relocation process if you come from another region and wish to move to Donostia\-San Sebastián (housing, job placement for family members, school enrollment, etc.). * You will enjoy a professional work environment truly distinguished by our humanity and closeness, where we care about diversity and inclusion. Diverse perspectives and your curiosity bring varied capabilities that strengthen our approach and drive our growth. * We take pride in offering equal opportunities. All individuals receive equal consideration for our open positions, regardless of gender, age, race, religion, identity, sexual orientation, origin, disability, or any other characteristic.

Cristina-Enea Parkea, 3, 20012 Donostia, Gipuzkoa, Spain

Negotiable Salary

Railway Maintenance Engineering Project Manager63839212426241128

Indeed

Railway Maintenance Engineering Project Manager

Are you looking to grow as a Maintenance Engineer, actively participating in project decisions and doing so alongside an experienced team in a close and supportive work environment? This is your opportunity! If you want to work towards a more sustainable and responsible world, at CAF we focus on sustainable mobility, one of the main challenges facing today's society. More specifically, within our Rail Services business, we are dedicated to the assurance and maintenance of railway vehicles. **What will be your mission at the company?** You will join the Projects team of the Metro Product Line with the following responsibilities: * Technical management of all Maintenance Engineering activities required under the contract, from optimizing maintenance documentation to industrializing workshop operations (PMGMAO). * Technical support to different Rail Services areas (Procurement, Finance, Quality). * Technical support to Operations during meetings with clients. * Technical support in the digitalization of maintenance processes in workshops. **What will make you succeed in this role?** * An Engineering degree due to the high technical content of the position and product. * A high level of English; knowledge of German and/or French is valued, as you will have continuous contact with internal and external foreign clients via video calls, emails, and in-person visits. And not forgetting our roots—the Basque language, which you can use in your daily work. * Experience in the railway sector or in maintenance of industrial equipment or facilities will be considered a plus. In summary, if you are interested in working to create a more sustainable and environmentally responsible world as part of our maintenance engineering team, apply for this position now.

Vial Camino Beasainmendi, 0A, 20200 Beasaimendi, Gipuzkoa, Spain

Negotiable Salary

Indeed

Manufacturing Engineer

**MAGOTTEAUX**, a multinational group with global presence and world leader in its field, is seeking for its plant in **Navarra** a candidate to fill the position: **MANUFACTURING ENGINEER, Ref.: 25064** Reporting to the Technical Management, the selected candidate will be responsible for designing the manufacturing setup of new products and driving their continuous improvement by developing appropriate procedures, methods and technologies, as well as solving problems through coordination and collaboration with other departments. To achieve this, advanced technologies will be used, including automated manufacturing of casting molds and core boxes, robotic scanning, and 3D model analysis software. **Main Responsibilities and Functions:** * Actively participate in the development and proposal of improvements for manufacturing processes and equipment, ensuring compliance with specifications for new products or the updating and enhancement of existing ones. * Identify and design new tooling and components required for upgrading and improving equipment and production lines, as well as all necessary auxiliary means, technical resources, and support tools according to each project. * Define new appropriate procedures, methods, and work instructions aimed at ensuring quality and optimizing manufacturing costs. * Collaborate with Production during the implementation of process changes and updates, monitoring compliance with defined specifications and guidelines, identifying issues and deviations, and implementing solutions to promote continuous improvement. * Assess and consider risks and opportunities associated with various improvement projects related to processes, equipment, facilities, methods, etc. * Prepare budgets related to tooling, installations, and other required resources for manufacturing. * Carry out all tasks in alignment with the company's strategic policies and plans regarding health and safety, quality, and environmental management. **Requirements:** * Engineering degree. Mechanical specialization is an advantage. * Professional experience in industrial environments involving manufacturing processes; knowledge of foundry and alloys is valued. * Proficiency in CAD/CAM design software. * English language proficiency. Knowledge of French is a plus. **We Offer:** A solid and stable career opportunity with excellent conditions within an international organization offering significant professional development potential. Internal training in manufacturing processes and specific foundry industry knowledge is planned. Position type: Full-time, Permanent contract Work Location: On-site

Caracter, C. Kortela, 16, 31810 Urdiain, Navarra, Spain

Negotiable Salary