QC RM- Sr. Officer
QC RM- Sr. Officer
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Job Description
Sampling & Analysis: Conduct chemical and instrumental analysis (e.g. HPLC GC UV FTIR wet chemistry) of raw materials following SOPs and pharmacopoeias (IP BP USP ).
Documentation: Prepare and review raw data sheets COAs logbooks and test reports ensuring accuracy and compliance with data integrity principles.
Review & Verification: Verify test results and ensure timely release of raw materials for manufacturing use.
Instrument Handling: Operate and calibrate instruments such as HPLC GC UV and IR and report any malfunction for timely resolution.
Deviation Handling: Report and investigate OOS/OOT results deviations and non-conformities supporting implementation of CAPA.
Audit & Compliance: Ensure all activities and documents are audit-ready and compliant with regulatory expectations (USFDA MHRA WHO EU-GMP).
Training & SOP Compliance: Ensure adherence to SOPs GLP and GMP guidelines and participate in training of junior analysts.
Required Experience:
Senior IC
Employment Type
Full-Time
