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Recruiting Top Talent Across the Global In The Life Science Industry
Are you an experienced QA professional with a strong background in GMP/GDP? Do you thrive in a dynamic environment where you can drive quality excellence in pharmaceutical development and commercialization? If so, this could be your next career move!
Apsida Life Sciences is currently seeking a QA Manager for a 12-month contract position.
Key Responsibilities:
* Provide GMP/GDP expertise throughout product development and commercialization.
* Ensure compliance with quality standards at every stage of the product lifecycle.
* Lead investigations (deviations, OOS, complaints) and implement CAPA measures.
* Apply quality risk management (Six Sigma principles) to optimize processes.
* Oversee batch record review, change controls, and product release activities.
* Collaborate with CMOs & CMC teams to draft and review GMP/GDP agreements.
* Contribute to SOP development and continuous improvement of the pharmaceutical quality system.
Ideal Candidate:
* Master’s degree in Pharmacy, Chemistry, or related scientific/technical field.
* 5+ years in pharmaceutical QA, with experience in drug substance/product development, manufacturing, or QC.
* Strong knowledge of (c)GMP/GDP regulations and industry best practices.
* Proven ability to manage complex projects, prioritize tasks, and drive quality initiatives.
* Excellent communication, leadership, and stakeholder management skills.
Duration: 12 Months
Seniority level
* Associate
Employment type
* Full-time
Job function
* Quality Assurance, Product Management, and Manufacturing
Industries
* Health and Human Services, Pharmaceutical Manufacturing, and Wholesale Drugs and Sundries
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