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Tier-1 pharma brand plus mid-level QA role in a metro location increases candidate competition.
Requires GMP, regulatory and batch-release expertise specific to pharma manufacturing, limiting transferability.
Explicit 6+ years requirement plus GMP, batch release, and regulatory compliance mandates strict candidate filters.
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Owns quality assurance compliance and GMP adherence for Pfizer products at Zydus Hospira Oncology Pvt Ltd (ZHOPL) site per Quality agreement.
Responsible for batch record review, release authorization, complaint management, and regulatory change control processes for Pfizer products manufactured at ZHOPL.
Supports supplier quality management, QMS compliance (including investigations, training, and validation document review), and provides quality support for product launches and tech transfers.
Bachelor's or Master's in Pharmacy (B.Pharm/M.Pharm) or M.Sc.
Minimum 6+ years of experience in Quality Assurance related to manufacturing and packaging, validations, complaint handling, investigations, change controls, document management.
Strong understanding of quality systems and manufacturing processes relevant to pharmaceuticals.
Work Location: On Premise at ZHOPL site.
Experienced in leading batch release and regulatory impact assessments in pharmaceutical manufacturing environments.
Skilled in complaint management and electronic lab systems with ability to handle complex investigations and audits.
Familiar with using AI tools (like ChatGPT or Microsoft Copilot) responsibly to enhance problem solving and productivity in quality assurance functions.