Lead RAQA Specialist

Stryker
38 672 € - 48 968 € par an
Rhône, Auvergne-Rhône-Alpes
Temps plein
il y a 3 semaines
Work Flexibility: Hybrid

Are you ready to take the lead in driving quality and compliance at one of the world’s leading medical technology companies? Join Stryker’s France Distribution Center as a Lead RAQA Specialist and help ensure we deliver life-changing medical devices with the highest standards of quality and regulatory excellence.

Key Responsibilities:

As a Lead RAQA Specialist, you will play a central role in ensuring regulatory compliance and quality. Your core responsibilities will include:

  • Implementing and maintaining the Quality Management System (QMS) in accordance with ISO 9001 standards, Stryker global guidelines, and internal procedures.

  • Driving continuous improvement by managing non-conformances, corrective and preventive actions (CAPAs), and contributing to cross-functional quality initiatives.

  • Participating in the risk management process to identify and mitigate quality-related risks throughout the product lifecycle.

  • Leading the qualification and evaluation of suppliers and distributors, in line with the audit schedule and corporate requirements.

  • Planning and conducting internal audits and distributor audits, ensuring compliance and driving accountability.

  • Supporting external certification audits (e.g., ISO, notified bodies) and ensuring audit readiness at all times.

  • Ensuring document control and integrity of Quality Assurance documentation across the site.

  • Providing targeted QA support for key Stryker France processes, including fiches navette and sterilization activities.

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Qualifications & Requirements:

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To thrive in this role, we are looking for candidates who bring both technical excellence and leadership capability:

  • Bachelor’s or Master’s degree in Quality Assurance, Life Sciences, or a related field.

  • 5+ years of experience in Quality Assurance or Regulatory Affairs within the medical device or pharmaceutical industry, ideally with direct experience in distribution center.

  • Strong knowledge of ISO 9001 and experience implementing or maintaining Quality Management Systems.

  • Familiarity with ISO 13485 is a plus.

  • Proven experience in internal and supplier auditing (Lead Auditor certification is a plus).

  • Solid understanding of risk management methodologies and quality tools.

  • Strong organizational and communication skills, with the ability to collaborate across teams and influence stakeholders.

  • Fluent in English and French, both written and verbal.

Travel Percentage: 10%

Postuler
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