Chemistry & Pharma Job Opening @ Teva Pharmaceuticals

Chemistry & Pharma Job Opening @ Teva Pharmaceuticals

Msc Chemistry jobs, M Pharma jobs. Teva Hiring chemistry and Pharma candidates. Chemistry jobs 2019. Pharma jobs 2019. Teva Hiring Postgraduate Msc Chemistry and M Pharma candidates. Teva is a global pharmaceutical leader and the world’s largest generic medicines producer committed to improving health, so applicants willing to work with such a great company can apply for this job position. Check out all the details on the same below:

Job Title: Quality Assurance Specialist

Work Location: Gajraula, IN, 244235

Eligibility: M.Sc Chemistry/BE Chemical/M.Pharma

Experience: Exp-2-4 Years

Job Description

  1. Review and approval of executed / masterbatch cards and other production-related data.
  2. Control, distribution & Archival of all documents.
  3. Responsible for coordination and supervising dispatch and related activities.
  4. Responsible for initiation, review of change controls system related to process, monograph, facility, SOP’s, vendor etc.
  5. Coordinating for investigating, review and closing of deviation, OOS, OOT, CAPA and related task. Follow up and implementation CAPA with effectiveness verification.
  6. Coordination and review of Qualification/Validation documents and engineering files and related task.
  7. Carrying out quality system audits / internal audit to verify compliance with principles of quality system GMP / GLP.
  8. Coordination, review and archival of technology transfer documents. Review and update of time limitation and process parameters.
  9. Coordination in stability sample initiation for validation batches, annual batch and others.
  10. Review and verification of documents and updation in the computerized system.
  11. Filling of Customer Questionnaires and other customer-related Queries.
  12. Responsible for preparation and review of annual product review.
  13. To perform the risk assessment.
  14. Batch card auditing & retrieval.
  15. To ensure the cGMP compliance and compliance of audit CAPA.
  16. Plant QA round for monitoring cGMP compliance.
  17. Carrying out of Basic GMP, Refreshing GMP, data integrity and SOP training to all company employees and contract workers.
  18. Performing and coordinating Vendor qualification/approval activities.
  19. Preparation of Approved manufacturer list.
  20. Any other job assigned by Site QA head / Head of Quality Function TAPI India.

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