Analytical Development
vor 1 Woche
Job Title:
Analytical Development - Quality Control Manager (ADQC)
Location:
Switzerland
Contract Type:
12 Month (FTC)
Company Overview:
Apsida Life Science is proud to partner with a global innovator to find a leader who can own the science of success. Step into a strategic role within their innovation hub, directing the Analytical Development (AD) and Quality Control (QC) roadmap for both Drug Substance (DS) and Drug Product (DP). Your expertise in strict GMP compliance will directly influence product integrity.
The Opportunity:
- Lead AD/QC for an assigned CMC program in late-stage (Phase 3)
- Act as the primary contact and supervisor for analytical CMOs/CROs and oversee the development and implementation of analytical methods.
- Regulatory Filings of draft and review source documents for IND, IMPD, and NDA/MA submissions.
- Lead troubleshooting, deviations, CAPA, and special investigations.
What you will Need:
- Master's degree in Chemistry, Pharmacy, Biochemistry is required, with a PhD or PharmD highly preferred.
- Mandatory strong background in analytical chemistry and broad knowledge of GMP/regulatory requirements.
- Proven experience developing and performing analytical tests.
- Ability to manage professionals effectively in a matrix system and act as an individual contributor or team leader.
What you get:
- Competitive salary
- Impactful work
- Real growth
- Work-life balance
- True inclusion
- Sustainable future
If you are interested in learning more, please reach out to Linda Goba at Apsida Life Science:
Apsida Life Science is a specialist recruitment business based in London (UK), Redhill (UK), Boston (USA) & Pretoria (South Africa) that is dedicated to delivering the best talent to the Life Science industry. We believe there is a gap in the market for a cost effective, high quality and trusted recruitment service that puts the candidate journey at the heart of the recruitment process.
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