Experience in production planning, change control, line clearance, deviation handling, autoclave operation, aseptic and controlarea operation, documentation, both SVP andLVP manufacturing etc.
To conduct the CAPA effectiveness review activities at manufacturing sites of Sun Pharma as per the review plan. To perform CAPA effectiveness review for CAPAs provided to Regulatory Authorities.
Saveetha College of Pharmacy, Saveetha Institute of Medical and Technical Sciences (SIMATS), Chennai; with a focus on strengthening compliance and promote a culture of quality within the pharmaceutical industry and academia; observed and celebrated theIndian Drug Manufacturers Association (IDMA)3rd National Current Good Manufacturing Practices (cGMP) Dayjointly in association with the Indian Pharmaceutical Association (IPA) Hospital Pharmacy Division, held on October 10, 2025; by organizing an Expert Talk and cGMP Sensitizing Program emphasizing the critical role of current Good Manufacturi
The U.S. Food and Drug Administration (FDA) has acknowledged reports of severe and ongoing contamination involving diethylene glycol (DEG) and ethylene glycol (EG) in children’s cough and cold medicines in India. The agency confirmed that these contaminated products have not been shipped to the United States.
HTLV‑1 – the first human retrovirus to be identified, in 1977 – affects at least 5-10 million people globally. It is concentrated in western and central Africa, Latin America, and the Western Pacific Region.
The candidate must have a M.S / M.Pharm. / degree in Medicinal chemistry / Natural Products / Pharmaceutical Analysis / Pharmacognosy from a PCI / AICTE / UGC / NAAC recognized / accredited University/Central Autonomous Institutes.
Bachelors degree or higher in Engineering/ Technology/ Pharmacy from a recognized University/ Institute. Applicants having an additional degree of MBA or equivalent would be given due preference.