FULLTIME
QA Executive

Puniska Injectables
Not specified · onsite · Posted 12d ago
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Section · 01
About this role
Job Summary
Responsible for ensuring quality, GMP and regulatory compliance across pharmaceutical manufacturing and packing operations. The role involves IPQA, batch documentation, quality system compliance, investigation of quality events and coordination with cross-functional teams to maintain product quality and compliance.
Roles & Responsibilities
- Perform IPQA activities and ensure GMP compliance on the shop floor.
- Conduct line clearance and verify manufacturing/packing activities as per approved procedures.
- Review BMR/BPR, logbooks and other batch-related documents.
- Handle deviations, incidents, OOS/OOT investigations and CAPA.
- Review and coordinate Change Controls and quality-related actions.
- Ensure compliance with SOPs, GDP and data integrity requirements.
- Support internal, customer and regulatory audits.
- Coordinate QA-related training and maintain training records.
- Participate in validation, qualification and quality risk management activities.
- Monitor and follow up on audit observations and CAPA closure.
- Coordinate with Production, QC, Engineering and other departments for resolution of quality issues.
- Ensure timely completion of QA documentation and quality system activities.
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Section · 02
Skills
Section · Company
About Puniska Injectables

Puniska Injectables
Pharma
Ahmedabad
IN
₹4.3L PA avg
Avg at Puniska Injectables
About
Puniska Injectables Pvt. Ltd. is a new age pharmaceutical company, based out of Ahmedabad, Gujarat, India which was incorporated on 14th May 2022.Its headquarters is in Ahmedabad, Gujarat and its plant is located at Goa. Puniska has been incorporated for developing lifesaving pharmaceutical Injectables and intravenous formulations to cater to mass market demand of quality products for India and worldwide markets. Presently Puniska is supplying its Products in Indian market. However, Puniska intends to expand its reach globally by obtaining regulatory approvals from outside markets for its facility at Goa.
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