Posted:2 weeks ago|
Platform:
On-site
Full Time
Be the First to Apply Job Description Business: PPL Digwal Department: TSD Location: Digwal Job Overview: To perform Production actives as per GMP & Safety Travel Requirements : NA Reporting Structure Reports to Manager - TSD Key Stakeholders Internal: QC, QA, SCM & Safety External: NA Experience 6-8 Year Experience in manufacturing (API) as per Pharma Manufacturing GMP requirements. Responsibilities Key Roles & Responsibilities Initiation of change controls Prepare the new BMRs, BPRs & ECRs as per requirement. Revision of existing BMRs, BPRs and ECRs as per requirement. Monitor & close the CAPAs. To plan the daily activities in the concerned production blocks. Close the pre- action & post- actions related to change controls in trackwise. Initiation and of review of deviation and investigation reports. Review the executed BMRs, BPRs, ECRs etc. Indenting & receiving of new / executed BMRs, BPRs, ECRs etc. Provide the response to the internal / external parties comments & update the documents. Follow the safety precautions. Maintain discipline at the work place. Ensure effective implementation of the cGMP compliance and quality management system in the plant. Follow the cGMP system and provide the training on change documents, SOP, CAPAs related to investigations, deviation etc. as per requirement. Any other responsibilities assigned from time to time as per requirement. Qualifications Qualification : B.Sc (Chemistry) / M.Sc (Chemistry) / B.Tech (Chemical) Job Info Job Identification 5344 Posting Date 05/28/2025, 09:16 AM Apply Before 05/30/2025, 09:16 AM Degree Level Technical Diploma/A Level Job Schedule Full time Locations Piramal Enterprises Limited. Factory: Digwal, Medak, Telangana, 502321, IN Show more Show less
Piramal Pharma Ltd
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My Connections Piramal Pharma Ltd
Mumbai, Maharashtra, India
Salary: Not disclosed
Mumbai, Maharashtra, India
Salary: Not disclosed