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.

Key Responsibilities

• 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

Candidate Profile

Required Qualifications

• 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

Preferred Qualifications

• 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.