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Job description

Role & responsibilities • Ensure line clearance and GMP compliance during production • Conduct environmental monitoring and batch sampling • Issue/reconcile monitoring materials and documentation • Perform process/cleaning validation, media fills, and hold time studies • Investigate deviations, incidents, and report quality issues • Coordinate audits, crossfunctional teams, and maintain authentic records Required Qualifications • B.Pharm / M.Pharm / M.Sc (Chemistry) • 2-5 years of experience in IPQA , SOS activity • It is a shift Duty profile (1st , 2nd Shift and Night too) If Interested Contant No - 8487939192 / Karishma.r.kadu@zyduslife.com

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