You are hereOpening for Sr. Executive / Executive - QC, QA, Production (API or Formulations) in Alembic India | Walk in Interviews
Opening for Sr. Executive / Executive - QC, QA, Production (API or Formulations) in Alembic India | Walk in Interviews
Alembic Pharmaceuticals Limited, with an established presence in the Indian pharma industry has a proud, historical track record going back over 100 years. With a turnover in excess of Rs. 1200 crores today. Alembic has been keeping pace with changing times and paradigms. To realize our ambitious plans, we call upon dynamic, result oriented team members to join our API and Formulations manufacturing units.
To realize our ambitious plants, we call up on dynamic, result oriented team members to join our API and formulation manufacturing units located at panelav, near vadodara
Post: Sr. Executive / Executive - QC/QA/Production
Sr. Executive / Executive - QC / QA (API or Formulations)
Candidates should be M.Sc or B.Pharm with 2 to 7 years of experience in QC or QA department in API / Formulations regulated manufacturing company. Experience includes analysis of raw material, packaging, & finished products, handling HPLC, GC, IR & other sophisticated instruments. QA activities would include documentation, validation, internal & external audit, master documentation creation, handling customer complaints and other department related activities. Exposure to DQ, IQ, OQ, PQ & regulatory audits like USFDA, MHRA, TGA is desirable
Sr. Executive / Executive - Production (Formulations)
Candidates should be M.Pharm or B.Pharm or M.Sc. with 2 to 7 years of experience in production activities i.e. Coating / Compression / Granulation, Packaging etc., having experience in documentation as per cGMR WHO, MCC, MHRA, USFDA guidelines.
Sr. Executive / Executive - Production (API)
Candidates should be M.Sc. or B.Sc. or B.E. (Chemical) with 2 to 7 years of experience in an API manufacturing facility. Responsibilities include adherence to SOPs / instructions to meet production targets, maintain data in BMR and all production records, maintain good housekeeping and safety, make reports for shift in-charge. Knowledge of cGMP is essential.
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