Executive - Projects - Economic Zones - Nhava Sheva

DP World
India
Workplace: OnsiteFull timeFunction: Communications, PR & CommunityExperience: 4-8 yearsEducation: bachelorsSkills: []

Own GDP Quality Assurance for healthcare operations in the Economic Zones at Nhava Sheva, covering QA oversight of pharma receipt through dispatch and returns, including 2–8°C and 15–25°C cold-chain processes. Lead investigation and closure of deviations, non-conformances, CAPA, and change control, manage temperature excursions end to end, and support audits and document control. Also support qualification/validation activities and review engineering and sanitation-related quality items.

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DP World
DP World
14 hours ago

Executive - Projects - Economic Zones - Nhava Sheva

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Last checked: 5 hours agoStatus: Live

Job Summary

Own GDP Quality Assurance for healthcare operations in the Economic Zones at Nhava Sheva, covering QA oversight of pharma receipt through dispatch and returns, including 2–8°C and 15–25°C cold-chain processes. Lead investigation and closure of deviations, non-conformances, CAPA, and change control, manage temperature excursions end to end, and support audits and document control. Also support qualification/validation activities and review engineering and sanitation-related quality items.
Location: India
Workplace: Onsite
Employment Type: Full time
Job Function: Communications, PR & Community
Seniority: Mid level

Key Responsibilities

  • •Provide QA oversight of receipt, storage, picking, packing, dispatch, and returns of pharmaceutical products, including cold chain (2–8°C / 15–25°C) and release/quarantine decisions with status labeling and segregation.
  • •Manage temperature excursions end to end (investigation, impact assessment, customer/MAH notification, disposition) and maintain excursion logs and trends.
  • •Govern cold chain activities: mapping protocols and reports, data logger deployment and download, alarm review, calibration status of monitoring instruments, and verification of shipper/passive packaging.
  • •Own deviations, non-conformances, CAPA, change control, and quality risk management; drive root cause analysis and verify effectiveness before closure.
  • •Support qualification and validation (URS, IQ/OQ/PQ for chambers, equipment, and utilities) and review engineering, pest control, cleaning, and sanitation quality items.

Key Requirements

  • •B. Pharm / M. Pharm (preferred) or M.Sc. Chemistry/Life Sciences with demonstrated pharmaceutical quality exposure.
  • •4–8 years in pharmaceutical QA, including pharma manufacturing, C&F/distribution, or GDP-compliant warehousing / 3PL / FTWZ operations.
  • •Sound knowledge of GDP (WHO/EU/CDSCO), the Drugs & Cosmetics Rules, and customer quality/technical agreements; GMP awareness (Schedule M / WHO GMP).
  • •Hands-on experience with deviations, CAPA, change control, risk assessment, self-inspection, and document control, including cold chain, temperature mapping, and excursion management.
  • •Able to independently handle customer and regulatory audits and write investigation reports and customer responses.
Experience:4-8 yearsPharmaceutical QAPharma manufacturingGDPGMP3PLCold chain
Education:Bachelor's
Tech Stack:MS OfficeWMS

Company Brief

DP World
Global ports, terminals and logistics provider offering end-to-end supply‑chain, maritime services, freezones and technology-driven trade solutions across ports, inland terminals, logistics parks and digital platforms.
Industry: Ports & Port Operators
Company Size: Enterprise (1,001+ employees)
Revenue: USD 1B+
Growth: Established Company
Valuation: Decacorn (USD 10B+)
Funding: IPO / Publicly Listed
Headquarters: Dubai, United Arab Emirates
Founded: 2005
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