Executive Manufacturing QMS And Compliance Injectable
Talentmate
India
18th September 2025
2509-5537-83
Job Description
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.
Qualification: B.Pharm/M.Pharm
Experience: minimum 2-5 years experience in manufacturing QMS/Process review/Compliance.
Job Details
| Role Level: | Mid-Level | Work Type: | Full-Time |
|---|---|---|---|
| Country: | India | City: | Ahmedabad ,Gujarat |
| Company Website: | http://www.amneal.com | Job Function: | Sales |
| Company Industry/ Sector: |
Pharmaceutical Manufacturing | ||
What We Offer
About the Company
Searching, interviewing and hiring are all part of the professional life. The TALENTMATE Portal idea is to fill and help professionals doing one of them by bringing together the requisites under One Roof. Whether you're hunting for your Next Job Opportunity or Looking for Potential Employers, we're here to lend you a Helping Hand.
Similar Jobs
Disclaimer: talentmate.com is only a platform to bring jobseekers & employers together. Applicants are advised to research the bonafides of the prospective employer independently. We do NOT endorse any requests for money payments and strictly advice against sharing personal or bank related information. We also recommend you visit Security Advice for more information. If you suspect any fraud or malpractice, email us at abuse@talentmate.com.
Recent Jobs
View More Jobs
Copyright © 2025 TALENTMATE. All rights reserved.
