Job Description

Key Responsibilities:

Develop and update SOPs; ensure company-wide compliance. Prepare MSDS and technical specs in line with regulatory guidelines. Maintain product and raw material specifications. Conduct training sessions on quality standards and practices. Perform internal audits and support corrective actions. Review Batch Manufacturing Records (BMR) and approve for release. Check COAs, labels, and packaging for accuracy before dispatch. Ensure all quality documentation is complete and up to date.

Qualifications & Skills:

B.Sc./M.Sc. in Chemistry, Pharmacy, or related field. 2-5 years of QA experience in relevant industry. Knowledge of GMP, SOPs, and regulatory norms. Strong documentation and audit skills. Good communication and team coordination abilities.
Job Types: Full-time, Permanent

Pay: ?250,000.00 - ?450,000.00 per year

Benefits:

Health insurance Paid sick time Paid time off Provident Fund
Schedule:

Day shift
Supplemental Pay:

Yearly bonus
Work Location: In person

Speak with the employer

+91 9175654751