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Franco Indian Pharmaceuticals (FIPPL) is seeking a QC/Analytical role focused on instrument analysis (HPLC, GC, FTIR, UV, Dissolution) and calibration across tablets and finished products.
You will validate analytical methods, review QC documents, and support process, cleaning and stability validations in a GMP setting. SAP experience is required.
Expertise in analysis of key instruments handling like HPLC, GC, FTIR, UV, Dissolution etc.
Expertise in Calibration, Qualifications of key instruments like HPLC, GC, FTIR ,UV, Dissolution etc.
Expertise in Analytical Method Validation for related substance, Assay and Dissolution of Tablets, finished products.
Analysis of Raw/Finished product (tablet)/ Process Valdiation/ Cleaning Validation/Packing Materials/ Stability Samples as per laid down specifications.
Review of documents as per good laboratory practices in Q.C.
Candidate must have approved in chemical and instrumentation from FDA Maharashtra.
Working knowledge of SAP is required.