Within the QA Shared Services – Product Transfer team, you will play a key role in the successful execution of global manufacturing transfers. You will ensure regulatory compliance, support validation activities, and contribute to continuous improvement initiatives to deliver efficient transfers in terms of quality, cost, and timelines.

This is a 1-year fixed-term contract as part of a maternity leave replacement, with the possibility of extension.

• Support all types of manufacturing transfers, including supplier-to-supplier, supplier-to-Stryker, Stryker-to-supplier, and inter-site Stryker transfers

• Review and approve validation and qualification documentation

• Act as the Quality Assurance point of contact during scope definition, planning, and execution of supplier transfers

• Provide quality guidance related to applicable regulations, standards, and procedures

• Identify potential quality risks during transfers and propose effective mitigation solutions

• Collaborate with multiple divisions (T&E, Joint Replacement, Endoscopy) and contribute to quality best practices across the organization

• University degree in Engineering, Science or a related field

• Minimum 2 years of experience in Quality Assurance and validation, preferably in the medical device or pharmaceutical industry

• Strong knowledge of quality concepts, risk management tools, and regulatory standards (ISO 13485, FDA 21 CFR Part 820)

• Fluent in English

• Experience with Quality Management Systems (QMS) or Supplier Quality

• Excellent communication, presentation, and project management skills, with strong attention to detail

• Lean Six Sigma certification (ideally Green Belt)

Join an international and regulated environment, at the heart of high-impact quality transfer projects, contributing directly to the improvement of healthcare.