Job Description

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: ₹15,000.00 - ₹25,000.00 per month

Experience:

Manufacturing: 1 year (Required)
License/Certification:

FDCA approval in Tablets/Capsule Production (Preferred)
Work Location: In person