QA

Must know process validation cleaning validation verification and hold time studies. Candidate should also have exposure to EU, MHRA, and USFDA regulatory audits.

Candidates having hands-on experience in Analysis of Raw Material, Packaging Material, Finished Goods, Stability, Method Transfer and Laboratory Investigations. Should have sound knowledge of QMS like Deviations, Change Control, Vendor Management etc.

Stallion Laboratories incorporated in 1988 as an integrated private sector Pharmaceutical Formulation Manufacturer, has acquired an unmatched record of managing niche product in formulations with a WHO GMP approved production facility and GLP qualified stringent quality control.

Technician, Operators for Ampoule and Vial Filling & Manufacturing. Lyo Operators, AM/HVAC Engineer, Fireman, Electrical and Instrumentation Engineer, Wireman, Refrigeration, EHS and ETP Officer and AM

Candidates should have experience in Formulations regulated manufacturing company such as USFDA and MHRA, EU. Exposure to regulatory audits like USFDA, MHRA, EU is mandatory

Hiring for our Vaccine & Oncology plants based at Baddi. Candidates having experience in a regulatory Injectables facility can attend Interview for the following positions.

B.Pharm / M. SC in Chemistry / Biotechnology; Experience into Media Fill Activities Exposure into EM Monitoring as QA Knowledge about Sterility, MLT, BET, Water Analysis, Media Preparation; Analysis of Raw Material / Finished product / Intermediates / Stability / Instrumentation / Sampling

Handling HPLC, GC, IP, FP, Stability Calibration, Method transfer Handling LCMS, ICPMS, PSD, AAS Empower  QA Department

Evaluate the change control requests and the impact on the stability of the products. Review the stability data of the products and issue recommendations for the shelf life Prepare the stability protocols and annual stability summary review for finished products