Piramal Pharma is a global pharmaceutical company that is part of the Piramal Group, one of India’s leading multinational conglomerates. It specializes in providing innovative solutions in the areas of pharmaceutical products, drug discovery, and contract manufacturing services. Piramal Pharma operates across a wide range of therapeutic areas including oncology, cardiovascular, and central nervous system (CNS) disorders.
Walk in Details:
Inviting candidates for a walk-in drive
DESIGN YOUR DESTINY
9th February 2025 (Sunday)
9:00 Am – 3:00 Pm
Venue:Hotel – Ramada Ahmedabad.
Opp. Prahlad Nagar Garden | S G Road | Ahmedabad – 380015 – Gujarat | India.
M: 6260600524 (Anuj Yagik)
M: 8889694726 (Vijayraj Singh Chauhan)
Note: We are hiring for Piramal Pharma Limited, Pithampur site (Indore) M.P
Requirement Details:
1) Role:
QC- Sr. Executive/ Dy. Manager – RM/FG/Stability/AMV (Experience: 4 – 9 years)
Qualification
B.Pharma/M.Pharma/M.Sc (Chemistry)
Experience and Skills Required:
Experience:
• Candidate should have good exposure on QC instruments (HPLC/GC/LCMS, Dissolution, UV Spectrophotometer/ KF/ Autotitrator / Malvern analysis) and trouble shooting.
• Should have Strong knowledge of QC investigations (Lab incidents, OOS/OOT etc).
• Candidate with exposure of regulatory organization (USDA/MHRA) will be preferred.
Note: Kindly bring your updated CV, latest CTC details, last three months’ pay slips, highest qualification’s marksheet and passport size photograph.
2)Role:
IPQA – Executive / Sr. Executive – (Experience: 2-7 years of OSD Unit)
Qualification
B.Pharma/M.Pharma/M.Sc (Chemistry)
Experience and Skills Required:
Experience:
• Candidate should have strong understanding of OSD manufacturing processes and knowledge of cGMP and relevant regulatory requirements.
• Monitoring critical process parameters during manufacturing.
• Candidate should have sound knowledge of QMS – Incidents, Change control,
Deviations etc.
3)Role:
QA – Executive / Dy. Manager – Process Validation/ Technology Transfer/ Documentation/ Equipment Qualification / Computer System Validation
(Experience: 3-9 years of OSD Unit)
Qualification
B. Pharma/M.Pharma/M.Sc (Chemistry)
Experience and Skills Required:
Experience:
• Candidate should have good exposure of Process Validation, Technology transfer and Cleaning Validation.
• Should be familiar with APR preparation, QMS, Risk Assessment approach and current regulatory requirements
• Candidate should have good exposure of Qualification of manufacturing
Equipment (OSD is preferred), Utilities (HVAC, Water system etc.) and Computer System Validation.
• Should be familiar with Risk Assessment approach and current regulatory requirements.
