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QA Specialist II

QA Specialist II

LocationVisp, Switzerland
Business SectorBiotechnology
Contact nameAliyana Darwesh
Contact email
Job ref22692
Published18 days ago
QA Specialist

Currently working with a Global Biotech Client in need of support from a QA Specialist for high-level projects in Switzerland. This is an opportunity to work in a state-of-the-art facility with ground breaking technology for a 9-month contract (extension expected).
 
Interview + offer will take place this week and next, so get in touch ASAP if interested.
 
Key responsibilities:
  • Provide oversight for compliance of Change Controls, CAPA and investigations, OOS and deviations.
  • Conduct external audits of suppliers/vendors/off-site facilities.
  • Review and approve validation documents.
  • Review Master Batch Records (MBR) and supporting documents.
  • Perform review/release of batch records, as needed.

Requirements:
  • 3+ years of GMP experience
  • Strong background in QA commercial drug substance/drug product operations or cell therapy manufacturing experience
  • Experience with oversight of aseptic processing according to international regulations
  • Ability to work in a fast paced environment as an autonomous and team-oriented professional
  • Proficient in English, German is a plus

Start Date: ASAP
Location: Visp, Switzerland
Set-up: Hybrid