
Officer/Sr. Officer-QA (Documentation)
Stallion Laboratories Pvt Ltd
Ahmedabad, Gujarat, India
Posted on 31-10-2025
1 Vacancy
Description
- Ensure that all manufacturing processes comply with cGMP, GLP, and regulatory standards.
- Conduct in-process checks, line clearance, and batch record review.
- Monitor documentation accuracy and ensure timely completion of QA records.
- Perform deviation, change control, and CAPA (Corrective and Preventive Action) management.
- Coordinate with production, QC, and warehouse teams for quality-related activities.
- Assist in internal and external audits, including regulatory inspections.
- Review and approve SOPs, validation protocols, and quality reports.
- Ensure proper implementation of quality systems and maintain product traceability.
- Train employees on quality policies, GMP, and hygiene practices.
Category
Pharmaceuticals
Functional Area
Pharma Quality Assurance (QA)
Key Skills
Good Communication SkillsAttention to DetailDecision-Making SkillsProblem Solving Skills
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