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Amneal Pharmaceuticals
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Executive Manufacturing QMS and compliance Injectable

Executive Manufacturing QMS and compliance Injectable

Amneal Pharmaceuticals

2 - 5 years

Ahmedabad Gujarat India

Posted:3 weeks ago

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Job Description

Key Responsibilities:

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.

Qualifications

Qualification: B.Pharm/M.PharmExperience: minimum 2-5 years experience in manufacturing QMS/Process review/Compliance.

Skills Required

manufacturing compliance reports management training audit kaizen

Work Mode

On-site

Job Type

Full Time

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Executive Manufacturing QMS and compliance Injectable