QMS Officer/Executive
Job Description:
Key Responsibilities:
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Handle QMS activities including CAPA, Change Control, Deviation, and OOS/OOT.
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Prepare, review, and maintain QMS documentation as per cGMP and regulatory guidelines.
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Support internal audits, external audits, and regulatory inspections.
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Ensure timely closure of quality incidents and continuous improvement initiatives.
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Coordinate with cross-functional teams for compliance and quality culture.
Requirements:
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B.Pharm / M.Sc (Chemistry) with 3–6 years of QMS experience in pharma formulation industry.
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Sound knowledge of cGMP, documentation practices, and regulatory standards.
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Strong communication and documentation skills.
Why Join Us?
Opportunity to work in a dynamic formulation setup with exposure to global quality standards and career growth.
Key Skills :
Company Profile
Our client followa standards of WHO - CGMP
Our Mission
“To become a valued Pharmaceutical partner to the World Pharma fraternity by continuously researching, developing and manufacturing a wide range of pharmaceutical products that complies with the global regulatory standards.”
Apply Now
- Interested candidates are requested to apply for this job.
- Recruiters will evaluate your candidature and will get in touch with you.