QA

Lincoln Pharmaceuticals Ltd., Ahmedabad based 40 years old, public limited having presence in 75+ countries, 1700+ registered products, own Manufacturing and R&D center and among india’s top 70 pharma company.

Responsible for monitoring and ensuring quality of products and comply with cGMP standards. Monitoring of critical process parameters, line clearance before batch initiation, verification of RM and equipment. In process sampling for quality check like pH, moisture content, and reaction monitoring.

Pharma Graduate with 2-8 years of experience in tablet and Liquid sterile manufacturing and Production QMS. Track and Trace systems, Manufacturing, Compounding of Nasal Spray formulations, vial Washing and filling machines. Having Good experience on online documentation and Knowledge to work in GMP environment.

The candidate will be responsible for preparation and submission of dossiers for NCEs and NBEs and will present it to relevant internal and external stakeholders. The candidate will represent the company with Indian regulatory agencies, including CDSCO, RCGM, Central Bureau of Narcotics and Karnataka drugs control department.

After a journey of growth spanning 27 years as Cadila Healthcare Ltd. and the Zydus Group, we have evolved and transformed ourselves in response to the changing times.

Centaur Pharmaceuticals one of the rapidly growing Pharmaceuticals Company in India. Centaur Pharmaceuticals is USFDA and MHRA approved plant is seeking deserving candidates having experience working in Oral Solid Dosage Manufacturing facilities for regulatory market's.

Bharat Technology is a premier college in Howrah, West Bengal with 19 years of academic excellence. Presently we are conducting fulltime Pharmacy courses like M.Pharm., B.Pharm and D.Pharm.

Candidate should have experience in Oral formulations Solid and liquid for Handling of IPQA, APQR activity and Process Validation. Candidates must have experience in review of Analytical Document, Investigating out-of-specification results, and ensuring adherence to GMP guidelines.

M. Pharm Pharmaceutical Quality Assurance, Pharmaceutics, Industrial Pharmacy and Ph.D. in relevant discipline, preferably in Pharmaceutical Quality Assurance. fresh and experienced; good track record of publications, patents, grants