Technical Responsible for Medical Device Manufacturing

hace 1 semana


Madrid, España PQE Group A tiempo completo

OverviewAre you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? As part of our ongoing growth and commitment to excellence, we are currently looking for a Technical Responsible for Medical Device Manufacturing to support the production of high‑quality medical devices and ensure compliance with regulatory and quality standards.ResponsibilitiesProvide support in plant authorization processes and ensure adherence to regulatory requirements for medical device manufacturing.Review finished products and decide on their release or rejection based on established quality and regulatory criteria, specifically for products involving liquid nitrogen used in cryopreservation and tissue conservation .Maintain accurate documentation and support the implementation and continuous improvement of the Quality Management System in accordance with medical device regulations such as ISO 13485 and EU MDR.Offer technical guidance to production and quality teams, ensuring that manufacturing processes remain compliant and efficient.QualificationsPrevious experience working with medical devices involving liquid nitrogen, specifically for cryopreservation and tissue conservation .Degree in Engineering, Biotechnology, Life Sciences, Pharmacy, or related fields.Solid understanding of medical device regulatory requirements and quality systems.Proficiency in English; Spanish is an advantage.Selection ProcessUpon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. If there's a positive match, a technical interview with the Hiring Manager will be arranged. If the outcome is positive, the recruiter will contact you for further steps or to discuss our proposal. Alternatively, if the outcome is negative, we will contact you to halt the recruitment process.OpportunityPQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world.#J-18808-Ljbffr



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