Piramal Pharma Limited is the Contract Development and Manufacturing arm of Piramal Pharma Ltd., with operations across North America, Europe and Asia. We are a global leader in integrated solutions and offer a unique platform of services across the drug lifecycle – from drug discovery and development to commercial manufacturing of drug substances and drug products. Piramal Pharma Limited, one of the leading pharmaceutical manufacturing companies in India, Piramal Pharma Limited offers a portfolio of innovative healthcare solutions through end-to-end manufacturing capabilities across 14 global facilities.
We have Hiring for Quality Control / Quality Assurance Professionals at Piramal Pharma Limited
- Department: Quality Control / Quality Assurance
- Designation: Executive
- Qualification: B.Sc, B.Pharm
- Experience: 3 to 7 year(s) of Experience
- Location: Indore
Related Jobs: Honour Lab Limited – Walk-In Interviews for Production / QC / QA / EHS / Engineering / Warehouse / PPIC / Technical Service (TSD) on 4th & 5th Feb’ 2023
Job Description:
1. QMS Investigations:
A. Should have sound knowledge of laboratory QMS investigations like, incidents, OOS/OOT, Change control, Deviations etc.
B. Responsible to handle the team of about 12-15 peoples.
C. Responsible to allocate work and analytical data review.
D. Candidate Should have sound knowledge of stability studies in formulation regulatory plant.
2. Analyst: HPLC-GC – RM
A. Analysis of Raw Materials and related documentation as per cGMP requirement.
B. Analysis of Vendor Approval Samples.
C. Sampling of RM/PM materials, testing and documentation as per cGMP requirement, analysis of samples for PSD using Malvern mastersizer, AAS etc.
D. Sound knowledge of HPLC/GC operations.
E. Calibration of laboratory relevant instruments, as and when required.
Related Jobs: Hetero Labs Limited – Walk-In Interview for Freshers & Experienced B.Sc, B.Pharm, M.Sc, M.Pharm, B.Tech, ITI, Diploma – Production / Packing / Stores / QA on 4th Feb’ 2023
3. Analyst: HPLC-GC- FG
A. Analysis of Finished products / Stability samples and related documentation as per cGMP requirement.
B. Analysis of cleaning validation samples.
C. Sound knowledge of HPLC/GC operations and aware about the analytical techniques like; Dissolution, Content Uniformity, Impurities test analysis.
D. Calibration of laboratory relevant instruments, as and when required.
WALK-IN INTERVIEW DETAILS: