Executive - Projects - Economic Zones - Nhava Sheva

Essential

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B. Pharm / M. Pharm (preferred) or M.Sc. Chemistry/Life Sciences with demonstrable pharmaceutical quality exposure.

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4–8 years in pharmaceutical QA — pharma manufacturing, C&F/distribution or GDP-compliant warehousing / 3PL / FTWZ operations.

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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.

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Hands-on experience of deviations, CAPA, change control, risk assessment, self-inspection and document control; practical cold chain, temperature mapping and excursion management.

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Able to face customer and regulatory audits independently and write investigation reports and customer responses.

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SOP writing and implementation across departments; proficient in MS Office and comfortable on WMS and digital quality tools.