Position: Deputy Manager / Manager – Quality Control
Company Profile
We are among the Top 10 Pharmaceutical API Manufacturers in India recognized for our strong regulatory compliance global presence and commitment to quality. Our manufacturing facilities are approved by leading regulatory authorities and follow stringent GMP GLP and international quality standards. We cater to both domestic and international markets with a diverse portfolio of Active Pharmaceutical Ingredients (APIs).
Key Responsibilities
Plan and coordinate routine analysis for Raw Materials In-process Intermediates and Finished Products to ensure timely release.
Oversee overall QC laboratory operations ensuring optimum manpower utilization and smooth departmental functioning.
Approve/reject raw materials packing materials and finished products including review of COA and GRN.
Ensure compliance with specifications analytical test methods SOPs GLP and regulatory requirements.
Handle OOS OOT deviations incidents and audit trail reviews in compliance with 21 CFR Part 11.
Ensure timely calibration qualification (IQ/OQ/PQ) AMC and maintenance of QC instruments.
Conduct method validation verification troubleshooting and specification revisions as per pharmacopeial updates.
Review validation protocols APQR QMS documents and analytical reports before submission to QA.
Coordinate internal customer and regulatory audits; support market complaint investigations.
Ensure proper documentation control samples management reference standards qualification and computerized system validation (CSV).
Provide training to QC staff and ensure adherence to safety health and environmental norms.
Position: Deputy Manager / Manager – Quality ControlCompany ProfileWe are among the Top 10 Pharmaceutical API Manufacturers in India recognized for our strong regulatory compliance global presence and commitment to quality. Our manufacturing facilities are approved by leading regulatory authorities ...
Position: Deputy Manager / Manager – Quality Control
Company Profile
We are among the Top 10 Pharmaceutical API Manufacturers in India recognized for our strong regulatory compliance global presence and commitment to quality. Our manufacturing facilities are approved by leading regulatory authorities and follow stringent GMP GLP and international quality standards. We cater to both domestic and international markets with a diverse portfolio of Active Pharmaceutical Ingredients (APIs).
Key Responsibilities
Plan and coordinate routine analysis for Raw Materials In-process Intermediates and Finished Products to ensure timely release.
Oversee overall QC laboratory operations ensuring optimum manpower utilization and smooth departmental functioning.
Approve/reject raw materials packing materials and finished products including review of COA and GRN.
Ensure compliance with specifications analytical test methods SOPs GLP and regulatory requirements.
Handle OOS OOT deviations incidents and audit trail reviews in compliance with 21 CFR Part 11.
Ensure timely calibration qualification (IQ/OQ/PQ) AMC and maintenance of QC instruments.
Conduct method validation verification troubleshooting and specification revisions as per pharmacopeial updates.
Review validation protocols APQR QMS documents and analytical reports before submission to QA.
Coordinate internal customer and regulatory audits; support market complaint investigations.
Ensure proper documentation control samples management reference standards qualification and computerized system validation (CSV).
Provide training to QC staff and ensure adherence to safety health and environmental norms.
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