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Head of Quality CQV Stein • Panda International
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Gevraagd
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37 - 40 uur
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Medior/Senior
Aanbod
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Vast contract
Vacature in het kort
Stein
Join a Greenfield project and lead the quality landscape at a major life sciences site. As Head of Quality CQV, you will guide a team of QA Experts and manage the integration of new production lines. This leadership role offers high visibility and career growth. You'll maintain the Equipment Qualification System, ensure compliance, and collaborate globally. Enjoy a permanent role with relocation support for eligible candidates. Interviews and offers are happening soon, so apply today! Read on to discover why this job might be perfect for you.
Over het bedrijf
Panda International
Bedrijfsprofiel
Volledige vacaturetekst
Are you looking for a unique opportunity to join a Greenfield project and shape the quality landscape of a major life sciences site? As Head of Quality CQV, you will be part of the Site Quality Leadership Team, leading a team of QA Experts and ensuring seamless integration of several new production lines into an existing manufacturing environment. This is a key leadership role with high visibility, impact, and career growth potential.
Responsibilities
- Establish and maintain the Equipment Qualification System, including commissioning, process validation, and qualification of manufacturing equipment and computerized systems
- Lead, develop, and mentor a team of QA Experts, fostering a culture of high performance and trust
- Ensure accurate qualification of equipment, infrastructure, and systems in compliance with regulatory requirements and internal procedures
- Act as main point of contact for qualification and maintenance-related documentation within QA
- Oversee compliance activities, including GMP status, supplier qualification, re-qualification, CAPAs, audits, and document management
- Collaborate with global and local teams to align and continuously improve CQV processes
- Manage resources effectively (budget, time, personnel, systems)
- Supervise supplier/service provider qualification and ensure adherence to quality agreements and audit requirements
- Degree or equivalent in Life Sciences, Engineering, or related field
- Several years of leadership experience (mandatory)
- Strong background in CQV and qualification within GMP-regulated pharmaceutical manufacturing
- Experienced in audits, including front-office participation (Swissmedic experience is a plus)
- Assertive decision-maker with the ability to uphold quality standards in fast-paced environments
- Start date: October (flexible)
- Location: Stein, Switzerland
- Contract type: Permanent, fulltime
- Language: English, German language skills are an advantage
- Location: Stein, Switzerland
- Relocation: Assistance available for eligible candidates and their families
Interested?
Interviews and offers can happen in the coming 2 weeks!
If you’re interested in the above description, please apply with your CV today. For further information, please contact Merel van Os at +31 (0)20 20 44 502 or by email at via de button "Solliciteer nu" op deze pagina.
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