PA Consulting seeks an experienced Medical Device Quality Specialist Consultant to support development and lifecycle management of medical devices and combination products. You will navigate regulatory complexity, embed robust quality systems, and ensure safety and compliance from development through post-market.
Strong consultancy experience and 8+ years in medical devices are valued. The role involves cross-functional teams, risk management per ISO 14971, and regulatory submissions across
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Senior Medical Device Quality & Regulatory Consultant employer: Whereby
Pleo is an exceptional employer that fosters a collaborative and innovative work culture, making it an ideal place for professionals looking to make a significant impact. With a strong focus on employee growth, Pleo offers ample opportunities for career advancement and skill development, particularly in the vibrant tech hub of [location]. The company values its employees by providing a supportive environment that encourages creativity and teamwork, ensuring that every team member feels valued and empowered to drive success.
