Head of Regulatory Compliance (FvP) - Biotech
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Permanent
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Exciting Biotech Products
Flexible work environment
About Our Client
Our client is a Swiss based Biotech company.
Job Description
- Qualify, evaluate and supervise suppliers, logistics service providers and CMOs
- Conduct audits and support inspections at suppliers, logistics service providers and CMOs
- Establish appropriate Quality Agreements
- Establish appropriate Quality Oversight principles for the contracted services
- Assess and coordinate release activities with release sites
- Ensure that the required HA licenses and GxP certifications are in place and up to date
- Host inspections by authorities
- Host customer audits
The Successful Applicant
- Proven track record of 5+ years in pharmaceutical industry internationally with at least 4 years GMP/GDP experience in a quality function, preferably as Responsible Person
- Sound knowledge of GMP/GDP, quality system requirements, as well as biopharmaceutical, Swiss and international (EU, US) pharmaceutical regulations
- Ideally trained as auditor and experience in supplier and CMO oversight and audits
- Fluent in both English and German
What's on Offer
- flexible work environment
- flat hierarchies
- great opportunity to build your own career within the business
- competitive salary package
PageGroup is an equal opportunity employer committed to workforce diversity, both as an employer as well as a recruitment service provider. Each recruitment decision we make for people we hire and people we place into new roles is based solely on the candidates’ knowledge, experience and skills.