- Perform in-process testing and sampling during mixing, filling, and packaging.
- Check pH, Brix, density, appearance, weight, sealing, labeling, and coding.
- Collect samples for chemical and microbiological analysis.
- Record and report results accurately and on time; escalate any OOS findings.
- Ensure compliance with GMP, GLP, and line clearance requirements.
- Maintain and calibrate QC/IPC equipment for accuracy and reliability.
- Collaborate with Production, QA, and Lab teams to resolve quality issues and support investigations and CAPAs.
B.Sc. in Science.1:5 years’ QC experience with IPC background in pharma, or sterile manufacturing.Good knowledge of IPC parameters, methods, and GMP/GLP.Skilled in lab techniques, documentation, SAP and MS Office.Fluent in EnglishExperience or background in IPC (In-Process Control).Familiarity with audits and document-related CAPAs.