Quality R&d Specialist - Fixed Term (10020)

Quality R&D Specialist (fixed term - 1 year) To be inserted in our team of Design Control for Drug Delivery Systems in Milan (IT). This person will be responsible for activities in the product development projects assigned, ensuring design control compliance with the QMS and applicable standards. They will review and approve all project deliverables in alignment with the team leader, examine design reviews, contribute to the next phase approval, and support regulatory registrations. Activities Execute activities to ensure product design development and transfer to Operations follow the design control process, acting as a team member of the product development projects and supporting the Design Team in technical decisions. Review and approve design control records, the design history file (DHF), risk management documentation, and other relevant documents. Act as a quality assurance expert, ensuring document completeness, accuracy, personnel competence, coherence of conclusions, and compliance with standards and regulations. Qualifications Academic background in biomedical engineering or similar fields. Experience in quality or R&D in medical devices or pharmaceutical companies is a plus. Fluency in English and Italian, both written and spoken, as you will work in an international team. Analytical approach and attention to detail. About Us We are a dynamic organization with great customers and a culture where people are valued and empowered to deliver excellent results. We are growing and seeking talented, passionate individuals to join our team! J-18808-Ljbffr

Location: Milano, Lombardia, IT

Posted Date: 8/20/2025