Job Description

Job Description

  1. Supervise compliance to all  cGMP, GxP, or any other regulatory requirements, including EH&S requirements.
  2. Complete self-training and monitor training of team members on the relevant SOPs
  3. Report any quality concerns or suggestions for improvements to Managers.
  4. Execute and supervise all tasks and activities as per the applicable SOPs.
  5. Responsible to complete the assigned trainings, applicable for workgroup “QA - Document review -GOA” in the L2LMS (SABA).
  6. Preparation/Revision of Standard Operating Procedures (SOP’s).
  7. Handling of customer requirements/ notifications.
  8. Handling of Market complaints, OOS, CAPA, change controls and deviations.
  9. Investigation and closure of Market Complaints, ADE’s, OOS, Failures and Deviations.
  10. Trending of Market complaints and OOS.
  11. Preparation/compilation of Monthly reports.
  12. To comply current EHS Management Systems of Site.

Work Experience

2-4 years experience.

Education

Graduation in Pharmacy
Masters in Pharmacy

Competencies


Job Details

Role Level: Associate Work Type: Full-Time
Country: India City: Panaji ,Goa
Company Website: http://www.lupin.com Job Function: General Management
Company Industry/
Sector:
Pharmaceutical Manufacturing

What We Offer


About the Company

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