QA/QC
GMP-driven quality assurance and analytical control.
01 —Role overview
QA and QC specialists own the systems and analytical work that ensure GMP compliance — from batch record review to release testing and stability programs.
02 —Key responsibilities
What you'll do.
- 01Review batch records and disposition manufactured product
- 02Execute release and stability testing per validated methods
- 03Operate HPLC, GC, dissolution, and spectroscopy instruments
- 04Maintain quality systems: deviations, CAPAs, change control
- 05Investigate OOS/OOT results and lead lab investigations
03 —Skills & tooling
In demand.
GMPHPLCGCMethod ValidationOOS InvestigationsBatch Record ReviewCAPALIMS
04 —Experience
Typical range
2–10 years
05 —Related roles
More in Pharmaceutical & Biotechnology.
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