Intas Pharmaceuticals hiring B.Pharma,M.Pharma,Msc – Apply!!

Intas Pharmaceuticals Ltd is Hiring for SENIOR EXECUTIVE – QUALITY ASSURANCE and has issued notification to accept Applications.Experience spanning three decades in healthcare, with a wide range of formulations to meet the needs of ailing humanity, Intas Pharmaceuticals headquartered at Ahmedabad (India), is now a force to reckon with, in the global pharma horizon..Application form link provided at the end of post. 

Vacancy summary details :

  • Company Name: Intas Pharmaceuticals Ltd
  • Location : India
  • Qualification: B.Pharma,M.Pharma,Msc
  • Experience: Preferred 6 to 8 year’s regulatory plant experience in Qualification Section.
  • No of Vacancies: NA
  • Details of Salary:  NA
  • Closing date for online Application : Apply as soon as possible
  • Date of examination: NA
  • Time and Venue :NA
  • Mode of application : online
  • Selection Process: Shortlisted candidates may called for selection process (  Personal interview , Group discussion , etc…,)

Job Description/Skills Required: 

  1. To do qualification / validation activities of Parenteral dosage form, documents preparation and review. 
  2. To maintain track of qualification and validation activities.
  3. To prepare and review the protocols and reports. Execution of various qualification / validation activities.
  4. To review correctness of the technical documents received from the supplier (DQ/OQ/IQ/PQ, FAT).
  5. Co-ordinate with production and other user department for qualification/validation activities
  6. Timely compile and review of qualification validation reports.
  7. To review the calibration & qualification reports and ensure correctness of documents.
  8. To perform FAT.
  9. To co-ordinate with outside agencies for execution of qualification activity whenever required.
  10. Identification of deviation through review and observation.
  11. To prepare annual Re-qualification/validation schedule, update VMP and Qualification related SOPs as and when required.
  12. Review of day to day and online compliance. Ensure compliance of GMP in validation/qualification section.
  13. Performing SAP transaction as required.
  14. Any other job assign as and when required.

Click here for notification and Apply

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