Posted:-1 days ago|
Platform:
Work from Office
Full Time
Key Responsibilities:
Perform routine and non-routine analysis using HPLC and other analytical instruments.
Review and maintain analytical documentation as per SOPs.
Ensure compliance with cGMP, GLP, and regulatory standards.
Support stability studies, method validation, and raw material/finished product testing.
Coordinate with QA, Production, and other cross-functional teams.
Required Experience & Skills:
34 years of hands-on experience in QC (API/Formulation).
Strong knowledge of HPLC, Dissolution, UV, and analytical troubleshooting.
Good understanding of GMP documentation and audit requirements.
Qualification: B.Sc / M.Sc (Chemistry) or relevant.
Bal Pharma
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