Job Overview
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Date PostedOctober 22, 2023
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Location (State / UT)
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Expiration dateMarch 14, 2025
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Experience5 Years, 9 Years
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GenderAny
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Desired QualificationBachelor Degree
Job Description
Roles and Responsibilities:
- Responsible for the Handling of market complaints at the site.
- Responsible for the Handling of Deviation management at the site.
- Responsible for the Handling of CAPA and Global CAPA management and effectiveness checking at the site.
- Responsible for coordinating the execution of mock recall and market recall.
- Responsible for reviewing and tracking Audit Responses.
- Responsible for raising, reviewing, and tracking Quality Alerts.
- Responsible for ensuring timely closure of QMS documents.
- To perform activity as per authorization in EDMS, LMS, and TRACKWISE software.
- Responsible for performing IPQA APQR activities.
- To perform process validation and cleaning validation sampling activity on the shop floor.
- To review new/exhibit/transfer and execute master BMRs and BPRs.
- To review batch records and associate annexures, checklists, etc.
- To perform Product/Recipe approval, SFG/FG release, sampling, sample posting, etc. in SAP HANA systems
- To prepare and execute hold time study protocol and perform sampling activity.
- To prepare and review process validation protocol and report.
- Preparation and Review of Annual product quality review.
Required Candidate Profile:
- B Pharma or M Pharma
- Mandatory 5-9 of Relevant Experience
Female Candidates Preferred
Note- Sun Pharma does not seek payment of any kind from prospective candidates for employment with Sun Pharma or authorize any agency or any individual to collect or charge any fees or charges for recruitment. Please be cautious while dealing with any recruitment agency or anyone asking you to pay money representing himself to be representing Sun Pharma.