Rusan is a research driven pharmaceutical company having its Manufacturing Units in India and Worldwide Marketing of Pharmaceutical Formulation, Active Pharmaceutical Ingredients and Intermediates. The company has its Corporate office at Kandivli (west), Mumbai, state of the art, Bulk Manufacturing Plant at Ankleshwar and Formulation plant at Dehradun and SEZ, Kandla having approval of Health Canada, EUGMP, EDQM.
Post : AGM
Location : Gandhidham Kandla SEZ, Gujarat
Experience Required : 15 to 20 Years
Salary : Competitive, as per market standards
Industry : Pharmaceutical
Plant Type : Formulation Unit (OSD + Injectables).
AGM - QA
Qualification : M.Pharm / B.Pharm / M.Sc
Strong knowledge of GMP regulations including WHO, EU GMP, PICS, TGA, MHRA, USFDA & other global regulatory guidlines.
Expertise in handling CAPA, CCF, deviations, market complaints, product recalls if any.
Experience in validation & qualification activities.
AGM - QC
Qualification : M.Sc / B.Sc / M.Pharm / B.Pharm
Expertise in lab management including handling lab incidents, deviations, change controls, OOS/OOT results.
Skilled in process and cleaning validation, hold time studies, stability studies as per company and client standards.
Ability to analyze product complaints and recalls with QA & production co-ordination
AGM - Production
Qualification : M.Pharm / B.Pharm / M.Sc
Proven experience in planning, organizing, and monitoring manufacturing operations for timely dispatch and yield control. Well-versed with cGMP compliance as per WHO, EU GMP, PICS, TGA, MHRA, USFDA regulations, Hands-on experience with process validation, product complaint, and recall handling with QA/QC departments
Candidates should be willing to relocate to Gandhidham, Gujarat.
Interested and eligible candidates are encouraged to send their updated resume to: corporatehr@rusanpharma.com
Last Date : 30th October 2025
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