Quality Assurance Executive
1 week ago
This position is responsible for managing all cGMP aspects of Quality Assurance Operations of a WHO-GMP approved Tablets and Capsule manufacturing facility.
Specific Responsibilities:
- In-Process Quality Assurance (IPQA) performing checks during manufacturing, such as sampling, manufacturing, packing, and line clearance,
- Review and approve SOPs, Batch Records, test methods, test results, labeling materials, specifications, analytical validation protocols and reports, stability protocols and reports.
- Review and approve records, including associated change controls, investigations (deviations, out-of-specification/out-of-trend), and analytical data.
- Understand and able to interpret regulatory authority regulations, guidelines and policies.
Qualifications / Requirements:
- Bachelor's degree in a scientific discipline (Masters Preferred).
- 2+ years of hands on experience in the pharmaceutical industry, with specific experience in GMP Quality Assurance
Job Type: Full-time
Pay: ₹15, ₹25,000.00 per month
Experience:
- Manufacturing: 1 year (Required)
License/Certification:
- FDCA approval in Tablets/Capsule Production (Preferred)
Work Location: In person
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