Job Purpose

To support and maintain Quality Management System (QMS) activities in vaccine manufacturing operations and ensure compliance with GMP and regulatory requirements.

Key Responsibilities

- Manage and review deviations, CAPAs, and change controls.
- Review Batch Manufacturing Records (BMRs) and production documentation.
- Ensure compliance with GMP, SOPs, and data integrity requirements.
- Support investigations and root cause analysis for quality issues.
- Coordinate document control activities, including SOP preparation and revisions.
- Participate in internal audits, self-inspections, and regulatory inspections.
- Monitor training compliance and maintain training records.
- Track quality metrics and prepare periodic reports.
- Support risk assessments and continuous improvement initiatives.




- Work closely with Production, QC, Engineering, and Warehouse teams.

Qualification

- B.Pharm / M.Pharm
- B.Sc / M.Sc (Microbiology, Biotechnology, Life Sciences)
- Equivalent qualification in Pharmacy or Biological Sciences

Experience

- 2 to 8 years of experience in QA/QMS, preferably in Vaccine, Biologics, or Sterile Manufacturing.

Job Snapshot

Updated Date

30-07-2026

Job ID

JOB6501

Department

MORAIYA VACCINE DP

Location

Manufacturing-formulation-moraiya, Ahmedabad, Gujarat, India ..+ 1

Experience

12 - 18 Years

Employee Type

C-C6-Confirmed-R&D; Executive

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