Sun Pharma Looking Bsc, Msc, BPharm, MPharm for Manager – CMO – QA apply now

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Sun Pharma Looking Bsc, Msc ,BPharm, MPharm for Manager – CMO – QA apply now 

Vacancy details:
  • Post Name:  Manager – CMO – QA
  • Qualification: MSc, BSc, M.Pharm, B.Pharm
  • Experienced: 9 – 14 years
  • Job Location: Mumbai
  • Salary :NA
  • Openings :NA
 Job Description: We have requirement for the post of Manager – CMO – QA in Sun Pharmaceutical Industries Ltd 

Contact Person: Vignesh Iyer
Kindly forward your profile to vignesh.iyer@sunpharma.com       
  • Responsible for review of batch related documents and release of Loan Licence products (Contract Manufacturing sites).
  • Preparation & review of specs and stp in DCM/LIMS.
  • Review of FG artworks.
  • Handling of deviations, change controls,OOS & OOT.
  • Visits to contract manufacturing sites to monitor manufacturing and testing is performed as per Sun Pharma Quality standards.
  • Preparation of visit report and ensure closure of discrepancies/gaps identified in the documents & system in coordination with site Quality management.
  • Participate in technology transfer along with FDD & MSTG. Review of validation data required to prepare validation report.
  • Preparation and review of stability protocol.
  • Monitoring ongoing stability study of LL products at contract manufacturing sites.
  • Product complaints are logged and communicated timely to respective contract manufacturing sites.
  • Thorough investigation of complaints with RCA and appropriate CAPA.
  • Participate in Investigation of critical and repetitive complaints along with site quality team.
  • Monitor implementation of CAPA as per committed timeline and effectiveness of CAPA.
  • Initiate quality alert and coordination with internal stakeholders to expedite the recall closure with appropriate documentation.
  • Evaluation /Assessment of impacted FG products/ Raw materials as per changes in monographs being reported in various Pharmacoepia from time to time. Track implementation of change at mfg.site.
  • Review of Product documents like BMR/BPR,FG test report, stability data, Process Validation Report, Analytical method validation report,APQR and etc.
  • Work experience on SAP,Trackwise,AMS,LIMS and DCM
  • 10-15 days travel in a month (average) to various contract manufacturing sites in India 
Selection ProcessThe selection will be on the basis of Interview.


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