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Executive Manufacturing QMS and compliance Injectable

3 - 8 years

6 - 10 Lacs

Posted:1 week ago| Platform: Naukri logo

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Work from Office

Job Type

Full Time

Job Description

Responsible for preparation & review of the master documents of sterile manufacturing for parenteral facility. Responsible for preparation and review of protocols and reports based on the requirements. Responsible for document management and preparation like BMR s, BPR s, master SOP s etc. Responsible for the handling of change control, deviations, CAPA, investigation etc. Responsible to give training to all the subordinates, technicians and operators of the department. Responsible for Audit and compliance on manufacturing shopfloor. Knowledge of kaizen and continuous improvements.

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Amneal Pharmaceuticals
Amneal Pharmaceuticals

Pharmaceutical Manufacturing

Bridgewater New Jersey

5001-10000 Employees

274 Jobs

    Key People

  • Chirag and Ameet N. Patel

    Co-CEOs
  • Kamran Alam

    CFO

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