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Vacancy description

Associate Manager - MQA upstream in Visakhapatnam, भारत

Pfizer

  • ContractFixed-term or freelance

Visakhapatnam, भारत

Associate Manager position in Manufacturing Quality Assurance at Pfizer's Vizag facility, overseeing cGMP compliance across sterile drug manufacturing operations including filling, washing, and depyrogenation. Requires 6-10 years of pharmaceutical manufacturing QA experience and responsibility for batch record reviews, investigations, and regulatory compliance.

Responsibilities

  • Ensure cGMP compliance in solution preparation, filling, capping, and collection operations
  • Review electronic batch records, assess manufacturing exceptions, and audit equipment trails
  • Conduct daily facility walkthroughs, monitor CCTV feeds, and report non-compliance observations
  • Perform manufacturing investigations, implement corrective actions, and ensure regulatory alignment
  • Lead interim team supervision and identify process gaps to improve efficiency and reduce downtime

Requirements

  • Bachelor's or Master's degree in Pharmacy or related life sciences field
  • 6-10 years of manufacturing quality assurance or production experience in pharmaceuticals
  • Knowledge of GMP regulations and sterile product manufacturing standards
  • Capability to handle regulatory inspections from FDA, MHRA, TGA and similar agencies
  • Technical writing skills for accurate and concise documentation
  • Proficiency with quality investigation tools and batch record systems
  • Strong interpersonal and written communication abilities across organizational levels

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