Job Description

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.