Deputy Manager Production QMS (OSD)

• Ensure implementation and compliance with cGMP SOPs and regulatory requirements in OSD manufacturing.

• Manage Production QMS activities including deviations investigations CAPA change controls and incident reporting.

• Review and ensure accuracy of Batch Manufacturing Records (BMRs) Batch Packaging Records (BPRs) and other production documents.

• Coordinate with QA QC Engineering and other cross-functional teams for timely closure of quality events.

• Conduct root cause analysis using appropriate investigation tools and ensure effective CAPA implementation.

• Support internal audits customer audits and regulatory inspections including USFDA and other regulatory agencies wherever applicable.

• Monitor recurring deviations documentation errors and process non-conformances; drive preventive actions.

• Ensure SOP preparation revision periodic review and implementation within the Production department.

• Support change management risk assessments and quality improvement initiatives.

• Ensure training and GMP awareness of production personnel.

• Maintain data integrity and good documentation practices (GDP) in all manufacturing activities.

• Prepare and monitor QMS-related metrics including deviation closure timelines CAPA effectiveness and audit observations.

Candidate Profile:

• Relevant experience in Production QMS within OSD formulations manufacturing.

• Strong knowledge of cGMP deviation management CAPA change control and regulatory compliance.

Qualification: B. Pharmacy / M. Pharmacy