Supriya Lifescience Limited headquartered in Mumbai, India is a public listed generic pharmaceutical company established in 1987 dedicated to developing, commercializing APIs & FDFs to treat patients with various diseases and infections. The API facility located at Lote, Maharashtra, India is multiple times USFDA, EDQM/EUGMP approved, and Health Canada approved whereas the Formulation facility located at Ambernath, Mumbai, India is EUGMP compliant. 

Production, FRD,QA, QC,RA & Maintenance

Production Department
Manufacturing Officer
Qualification : B.Pharm, M.Pharm 
Experience : 4 to 5 
Job Description : Installation/qualification of equipment. Manufacturing of Solid oral/ liquid/ injection dosage forms. Audit Handling (US,MHRA,ANVISA, GMP compliance
Manufacturing Executive/ Sr.Executive 
Qualification : B.Pharm, M.Pharm 
Experience : 4 to 6 
Job Description : Knowledge having : batch  observations / readings, environmental conditions, labeling, weighing. Inprocess checks and other required observation before / during / after In each compression and Bin feed area, coating and Inspection area., submission of SOPs/ BMRs / Records / logs / labels etc., SOP Related Trainings.
Manufacturing Technician / Operator 
Qualification : Production 12th, ITI, B.Sc, 
Experience : 2 to 4 
Job Description : 1. Compression operator who have handled Fette P3030 machine cadmach clOO
2. Granulation operator Who have handled HSM 150 and 500 (ACG make) FBE 150 and FBE 500 (ACG make). 
3.liquid filling operator
4. Vial line operator who have handled tofflon line
5. Caping of vial handling machine make Tofflon
6. Vacuum testing and visual inspection machine operator

FRD
Research Scientist 
Qualification : M.Pharm 
Experience : 3 to 5 
Job Description : We are seeking a highly skilled and experienced Formulation Development Scientist specializing in solid oral dosage forms. The ideal candidate will have extensive knowledge of immediate, extended, and delayed-release formulations, and be proficient in Quality by Design (QbD) principles. Process Development Report (PDR) preparation, and technical document creation.
Quality Assurance
Quality Assurance Officer / Executive 
Qualification : B. Pharm, M.Pharm 
Experience : 4 to 5 
Job Description : Having knowledge of Validation/Qualification activity, Knowledge of QMS documentations, Monitoring Aseptic / sterile manufacturing and process monitoring, SOP preparation and Review.
Quality Control
QC Analyst 
Qualification : B. Pharm, M.Pharm/Msc 
Experience : 4 to 5 
Job Description : Routine,stability analysis,Water Analysis, SOP Preparation & Review

Regulatory Affairs 
Asst./Dy. Manager Regulatory 
Qualification : B.Pharm, M.Pharm 
10 to 12 
To oversea development support, audit handling, dossier filing, query response for (US, Europe, Brazil, ROW), liasoining
Officer Regulatory
Qualification : B.Pharm, M.Pharm 
Experience : 5 to 7 
Job Description : To oversea development support, audit handling, dossier filing, query response for (US, Europe, Brazil, ROW), liasoining

Job Location : Ambernath Formulation
Walk in Interview
Date : TUESDAY dated 15/10/2024 
Time : 09:00 AM TO 04:00 PM
Venue : Hotel Nakshatra, Lot No. K-l, Additional MIDC, Near Anand Nagar, Ambernath (E), MH-421506
Important Notes
• Current pharma (formulation) background is must Good GMP, GLP Knowledge.
• Aware of all required regulatory norms, good in read, write & understanding of English language.
• Only relevant experienced candidates as per criteria mentioned are invited.
• All applicants kindly adhere to specified interview time.