Industry: Pharmaceutical Formulation Plant

Department: QA

Experience: 2– 4 Years

Location: Jarod - Savli Road, Vadodara

Job Responsibilities:

- Coordinate with factories and maintain records for product permissions, NOC, WHO certificates, manufacturing licenses and other regulatory documents.
- Ensure monthly batch closure for dispatched products.
- Manage product masters and quality documentation in PharmaCloud for third-party manufacturers and trading partners.
- Coordinate finished product sample verification and ensure compliance with approved specifications.
- Manage control samples and stability samples, including labeling, storage, environmental monitoring and scheduled withdrawal.
- Coordinate with QC for stability sample testing and monitor analytical results and release status.
- Follow up with factories for finished samples and verify GSM, text, color and artwork compliance.
- Coordinate with Purchase and factories for POs, draft composition,



product permissions and artwork initiation.
- Coordinate daily with designers, artwork teams and factories for artwork development and print proof approval.
- Maintain proper records and documentation for all regulatory, sample, artwork and product-related activities.
- Coordinate with QA, QC, Purchase, Production and third-party manufacturers to ensure timely completion of activities.

Qualification - B.Pharm / M.Pharm / B.Sc. / M.Sc. / relevant qualification. Skills: Regulatory documentation, pharmaceutical QA, artwork coordination, sample management, GMP/GDP, documentation and robust follow-up/coordination skills.

Interested Candidates can share their CVs on [email protected]

Benefits

- Food provided
- Health insurance
- Leave encashment
- Provident Fund

Work Location: In person

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