Executive Manufacturing QMS and compliance Injectable Amneal India

5.0 - 9.0 years

0 Lacs

ahmedabad, gujarat

On-site

Job Description: As a member of the team, you will be responsible for the following 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 BMRs, BPRs, master SOPs 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 improvem...

Posted 1 week ago

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Executive Manufacturing QMS and compliance Injectable Amneal Pharmaceuticals

3.0 - 7.0 years

0 Lacs

ahmedabad, gujarat

On-site

Role Overview: - You will be responsible for the preparation and review of master documents for sterile manufacturing in the parenteral facility. - Your role will involve preparing and reviewing protocols and reports as per requirements. - You will handle document management and preparation of BMRs, BPRs, master SOPs, etc. - Managing change control, deviations, CAPA, investigations will also be part of your responsibilities. - Providing training to subordinates, technicians, and operators in the department will be your duty. - Ensuring audit and compliance on the manufacturing shop floor. - Utilizing knowledge of kaizen and continuous improvements. Key Responsibilities: - Prepare and review ...

Posted 1 month ago

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Executive Manufacturing QMS and compliance Injectable Amneal Pharmaceuticals

3.0 - 7.0 years

0 Lacs

ahmedabad, gujarat

On-site

You will be responsible for preparing and reviewing the master documents of sterile manufacturing for the parenteral facility. Additionally, you will prepare and review protocols and reports based on the specified requirements. Document management and preparation tasks such as BMRs, BPRs, and master SOPs will also fall under your responsibilities. Handling change control, deviations, CAPA, investigations, and providing training to subordinates, technicians, and operators within the department are key aspects of this role. You will also be accountable for audit and compliance on the manufacturing shop floor. The ideal candidate for this position should hold a B.Pharm/M.Pharm degree and posses...

Posted 3 months ago

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