Manager- CMO

Position: Manager 2 - CMO

Department: Corporate Quality

Location: Mumbai/ Baroda

Reporting Manager Title: DGM- CMO

Job Summary:

• Accountable for quality oversight of contract manufacturing organizations responsible for manufacturing of site transfer products (Sun site RD) for US market.

Essential Job Functions:

• Regular oversight visits of the CMO sites for review of process practices and accordingly prepare visit reports.
• Coordinate with Sun site, commercial, corporate quality audit the CMO site as SPOC for activities related to product manufacturing and release and other technical issues.
• To author and review quality agreements between Sun Pharma CMO site. Also, ensure qualified and approved external service providers are used.
• To ensure presence and participation during manufacturing for process validation batches to ensure that the manufacturing process as per the approved BMR is followed.
• To witness testing of process validation batches including hold time studies and in-process testing are conducted as per the approved specification, test procedures protocols.
• Review of quality system documents, facility equipment s, manufacturing packing controls, labelling laboratory controls at the CMO site at regular intervals.
• Cause based /routine visits to CMO sites (with reference to Market Complaints/Recalls/CAPA implementation and effectiveness check)
• Review of batch manufacturing packaging records, analytical reports and COA/COC for batch release. And release of batches in SAP.
• Review of stability data, process validation report, analytical method validation report, specification/STP of FP, API COA, primary packing material COAs, approved vendor of RM/PM, APQR etc.
• To review quality system documents such as change controls, deviations, CAPA, OOS/OOT, product quality complaints, Recalls etc.
• Prepare review SOP s as per Sun Pharma quality standards.
• Prepare approved vendor list for raw materials and primary packaging materials for the product to be manufactured at the CMO site.
• To prepare annual risk assessment of the CMO sites.

Requirements and Qualifications:

• M.Sc./ B. Pharm / M. Pharm or equivalent.

Industrial Experience Knowledge:

• Total 15-18 years of experience in Quality Control, Quality Assurance, Quality and compliance, in sterile formulations manufacturing.
• Knowledge of GMP s in both domestic and international regulatory environments. In-depth knowledge of FDA guidance s such as ICH is must.
• Strong organizational, interpersonal and communication skills.
• Ability to work effectively in multicultural matrix organization