Executive - Projects - Economic Zones - Nhava Sheva

Essential B. Pharm / M. Pharm (preferred) or M.Sc. Chemistry/Life Sciences with demonstrable pharmaceutical quality exposure. 4–8 years in pharmaceutical QA — pharma manufacturing, C&F/distribution or GDP-compliant warehousing / 3PL / FTWZ operations. Sound working knowledge of GDP (WHO/EU/CDSCO), the Drugs & Cosmetics Rules and customer quality/technical agreements; GMP awareness (Schedule M / WHO GMP) sufficient to support value-added services and customer GMP audits.

Hands-on experience of deviations, CAPA, change control, risk assessment, self-inspection and document control; practical cold chain, temperature mapping and excursion management. Able to face customer and regulatory audits independently and write investigation reports and customer responses. SOP writing and implementation across departments; proficient in MS Office and comfortable on WMS and digital quality tools.