To support Corporate QA in ensuring compliance of all manufacturing sites with cGMP, GDP, regulatory guidelines, company SOPs, and quality systems, covering all dosage forms (Tablet, Capsule, Liquid, Ointment).
Skills & Competencies
Strong knowledge of cGMP, Schedule M, and pharma regulatory requirements.
Good documentation & communication skills.
Corporate review of
BMR/BPR
, master documents, and change control proposals.
Knowledge of Sterile and Non-sterile dosage forms advantageous.
Coordinate for
regulatory or customer audits and
ensure timely submission of required documents.
Proficiency in MS Office (Advance Excel, Word, PowerPoint).
Education & Experience
B.Pharm / M.Pharm / B.Sc / M.Sc
2-5 years
experience in QA (IPQA, Documentation, QMS, Validation, Audit) in a pharmaceutical manufacturing company.
Experience with
multiple dosage forms
preferred.
Key Deliverables
On-time review and control of QA documents.
Closure of audit observations and CAPA.
Up-to-date QMS tracking and reporting.
Support for successful regulatory audits.
Job Type: Full-time
Pay: ₹600,000.00 - ₹800,000.00 per year
Work Location: In person
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