Quality Assurance Officer

Full job description
To ensure compliance with cGMP, regulatory requirements, and company standards through implementation and maintenance of QA systems, documentation review, and quality audits.

Key Responsibilities:

Review batch manufacturing and packaging records for completeness, accuracy, and compliance with GMP.
Participate in investigations of deviations, non-conformances, CAPAs, and customer complaints.
Perform internal audits and assist with external regulatory and customer audits.
Support in the qualification and validation of equipment, utilities, and processes.
Manage controlled documents (SOPs, protocols, reports, etc.) within the document management system.
Monitor and enforce adherence to GMP and quality policies across the plant.
Review and approve change controls, risk assessments, and quality-related protocols.
Conduct training sessions on GMP and quality systems for relevant personnel.
Maintain QA metrics and generate periodic quality reports for management review.
Qualifications:

Bachelor’s or Master’s degree in Pharmacy, Chemistry, or related life sciences.
1–3 years of QA experience in the pharmaceutical industry (more for senior roles).
Knowledge of GMP, ICH guidelines, WHO, US FDA, or other relevant regulatory standards.
Good documentation and communication skills.
Proficient in MS Office tools and electronic documentation systems (preferred).
Desirable Skills:

Attention to detail.
Strong analytical and problem-solving abilities.
Team player with ability to collaborate cross-functionally.
Time management and organizational skills.
Job Types: Full-time, Fresher

Pay: ₹12,000.00 - ₹25,000.00 per month

Benefits:

Provident Fund
Schedule:

Day shift
Supplemental Pay:

Performance bonus
Work Location: In person Read more