Overview
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
Qualifications
* 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
Practicalities
* Language: English (German language skills are an advantage)
* Relocation: Assistance available for eligible candidates and their families
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 m.vanos@panda-int.com
Seniority level
* Director
Employment type
* Full-time
Job function
* Quality Assurance
Industries
* Biotechnology Research, Pharmaceutical Manufacturing, and Hospitals and Health Care
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