Senior Specialist, Qc Cell

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3+ years biopharma qc experience
2+ years gmp environment experience
Cell culture techniques (adherent/suspension)
The role involves participating in daily QC cell group inspections, management, and ensuring compliance with domestic and international regulations

Job Summary

  • The role involves participating in daily QC cell group inspections, management, and ensuring compliance with domestic and international regulations.
  • Candidates must organize method validation implementation and write verification reports to guarantee the effectiveness of analytical methods.
  • The position requires managing stability studies for intermediate and finished products while ensuring data integrity and reliability.

Matching Summary

The role involves participating in daily QC cell group inspections, management, and ensuring compliance with domestic and international regulations.

Skills & Requirements

Must-have

  • 3+ years biopharma QC experience
  • 2+ years GMP environment experience
  • Cell culture techniques (adherent/suspension)
  • Flow cytometry operation skills
  • Method validation and SOP drafting

Nice-to-have

  • CAR-T cell therapy experience
  • BD Canto or Lyric flow cytometer usage
  • OOS and deviation investigation experience
  • English writing for technical documents
  • T-cell and HeLa cell line experience

Key Requirements

  • Bachelor's degree in Pharmacy, Biology, or related field
  • Fluency in English including technical writing
  • Experience with CAR-T cell analysis preferred

Work Rights

Not specified

Tailored Resume

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