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Jobs at Intas Pharmaceuticals: Vacancies for Quality Assurance, Send your Resume Now

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Jobs at Intas Pharmaceuticals – Vacancies for Quality Assurance, Send your Resume Now.

Jobs at Intas Pharmaceuticals

About Company:

Intas Pharmaceuticals Ltd has been in the healthcare industry for thirty years. They make different kinds of medicines to help sick people. The company’s main office is in Ahmedabad, India. Intas Pharmaceuticals is now a big and important company in the world of medicine. They know a lot about making different kinds of medicines, like pills and shots, and even new ways to give people medicine. In India, they are ranked as the 17th biggest medicine company. Intas Pharmaceuticals does a lot of research to make new medicines and they have patents for their ideas. They also get approval from health regulators in many countries. This makes Intas a company that takes care of people’s health all around the world. To apply for Jobs at Intas Pharmaceuticals, Read all the details below.

Intas Pharmaceuticals Virtual walk-in Interview Details:

DepartmentsQuality Assurance
Experience2 to 10 Years (Candidate must have experience in API Pharma)
PositionOfficer / Sr. Officer / Executive
QualificationB.Pharm / M.Pharm / M.Sc
Job LocationValia

Skill Required:

  • Experience in Qualification, QMS, QC-QA, Regulatory Affairs & IPQA

Roles and Responsibilities

  • To perform equipment qualification and utility qualification activity with proper documentation.
  • To perform Computer system validation.
  • To investigate deviation, change requests, OOS, market complaints, etc.
  • To review & close Deviation, Change Control, CAPA, Out of Specification, and investigation.
  • To prepare & review Quality risk assessment reports.
  • To prepare process validation protocols & reports, cleaning validation protocols & reports.
  • To perform QC instrument qualification & Calibration.
  • To review analytical data, raw data if method validation and method transfer.
  • To review & closure of OOC, OOT etc with proper investigation.
  • To control the record & monitor all the activities for the stability chamber & retain sample Handling of regulatory deficiencies.
  • DMF updation as and when required by the regulatory department.
  • Global CAPA review and closure.
  • To perform IPQA activity.

How to Apply

Mail your CVs to [email protected]

Please Note: Intas Pharmaceuticals Ltd. does not directly or indirectly charge any fee for job application, processing, training, or testing. Do not participate in any such invitations.
The shortlisted candidates will be shared MS Teams link for interview discussion.

Website: Intas

Jobs at Intas Pharmaceuticals
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