Quality Management Coordinator

Title : Interim Quality Management Lead

Location : Hamburg, Germany (2 days home office)

Contact : [email protected]

The Company

Are you passionate about making a tangible difference in the medical device industry? This is your chance to join a unique, collaborative environment where innovation thrives.

Our client, a rapidly growing class III implantable medical device company located near Hamburg, is seeking an experienced Quality Management Lead to join their team.

With a mission to integrate groundbreaking solutions into their international operations, they need someone who isn’t afraid to tackle challenges head-on and lead with both expertise and purpose.

If you love fostering teamwork while driving excellence in quality standards, this could be the role for you.

The Opportunity

This 12-month freelance role is your chance to define and lead quality initiatives at a pivotal time. You’ll have the autonomy to implement new processes, correct deficiencies, and integrate systems into a larger global framework.

If you thrive in dynamic settings and love building expert teams while solving complex issues, this is your stage. Does this sound like the kind of challenge that excites you?

Your Responsibilities :

• Lead and mentor the Quality Management team, driving daily operations and fostering a collaborative culture.
• Implement innovative processes to enhance the QMS, ensuring seamless integration with global operations.
• Take charge of critical audits and inspections, correcting deficiencies and elevating standards.
• Serve as the expert in Quality Management Systems (QMS), providing hands-on support and strategic direction.

Your Qualifications :

• 8+ years of experience in Quality Management and Quality Control for medical devices.
• Ideally working in a manufacturing facility
• Fluency in German and English and ability to work on-site a minimum of 3 days per week

If you are interested in this exciting role, please send your application directly to [email protected] .

Please note : Due to the high volume of applications we sometimes receive, our team might not be able to contact each applicant individually regarding the status of their application.

If you do not hear from us after 10 days, please consider your application unsuccessful.

Key skills we recruit for :

ISO 13485, 21 CFR 820, CE marking, MDR, Medical device regulation, MDD, medical devices, Digital health, 510(k), PMA, Regulatory affairs, quality assurance, QA / RA, design quality, ISO 14971, combination devices, sterilisation, AIMDD, CER, PMCF

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