- Full Time
- Ambernath, Mumbai, Maharashtra
Website Supriya Lifescience
Table of Contents
ToggleAbout Supriya Lifescience
Supriya Lifescience Limited, headquartered in Mumbai, India, is a public listed pharmaceutical company established in 1987. We are dedicated to developing and commercializing Active Pharmaceutical Ingredients (APIs) and Finished Dosage Forms (FDFs) to treat various diseases and infections. Our API facility in Lote, Maharashtra, has multiple USFDA, EDQM/EUGMP, and Health Canada approvals. Our EUGMP-compliant formulation facility is located in Ambernath, Mumbai.
We are currently seeking qualified and experienced professionals for our Production, FRD, QA, QC, RA, and Maintenance departments.
Production Department
Manufacturing Officer
- Qualification: B.Pharm, M.Pharm
- Experience: 4 to 5 years
- Key Responsibilities:
- Installation and qualification of equipment.
- Manufacturing of solid oral, liquid, and injectable dosage forms.
- Handling audits from regulatory bodies (USFDA, MHRA, ANVISA) and ensuring GMP compliance.
Manufacturing Executive/Sr. Executive
- Qualification: B.Pharm, M.Pharm
- Experience: 4 to 6 years
- Key Responsibilities:
- Monitoring batch observations, environmental conditions, labeling, and weighing.
- Performing in-process checks and managing SOPs, BMRs, and relevant documentation.
- Conducting SOP-related training sessions.
Manufacturing Technician/Operator
- Qualification: 12th, ITI, B.Sc
- Experience: 2 to 4 years
- Key Responsibilities:
- Operating compression machines (Fette P3030, Cadmach C100).
- Managing granulation equipment (HSM 150/500, FBE 150/500, ACG make).
- Liquid filling and vial line operation with capping machines and vacuum testing.
Formulation Research and Development (FRD)
Research Scientist
- Qualification: M.Pharm
- Experience: 3 to 5 years
- Key Responsibilities:
- Specializing in the development of solid oral dosage forms, including immediate, extended, and delayed-release formulations.
- Proficiency in Quality by Design (QbD) principles and Process Development Report (PDR) preparation.
- Creation of technical documentation.
Quality Assurance (QA)
Quality Assurance Officer/Executive
- Qualification: B.Pharm, M.Pharm
- Experience: 4 to 5 years
- Key Responsibilities:
- Overseeing validation/qualification activities and QMS documentation.
- Monitoring aseptic and sterile manufacturing processes.
- Preparing and reviewing SOPs.
Quality Control (QC)
QC Analyst
- Qualification: B.Pharm, M.Pharm, M.Sc
- Experience: 4 to 5 years
- Key Responsibilities:
- Conducting routine and stability analysis, water analysis, and preparing/reviewing SOPs.
Regulatory Affairs (RA)
Assistant/Deputy Manager – Regulatory Affairs
- Qualification: B.Pharm, M.Pharm
- Experience: 10 to 12 years
- Key Responsibilities:
- Overseeing development support, audit handling, and dossier filing.
- Responding to regulatory queries for regions such as the US, Europe, Brazil, and ROW.
Regulatory Affairs Officer
- Qualification: B.Pharm, M.Pharm
- Experience: 5 to 7 years
- Key Responsibilities:
- Managing development support, audits, and regulatory submissions.
- Handling dossier filing and regulatory liaisons for global markets.
Job Location
- Ambernath Formulation Facility
Walk-In Interview Details:
- Date: Tuesday, 15th October 2024
- Time: 9:00 AM to 4:00 PM
- Venue: Hotel Nakshatra, Lot No. K-1, Additional MIDC, Near Anand Nagar, Ambernath (E), MH-421506
Important Notes:
- A background in the pharmaceutical (formulation) industry is essential.
- Good knowledge of GMP, GLP, and regulatory norms is required.
- Applicants should have proficiency in English (reading, writing, and comprehension).
- Only candidates with relevant experience as per the criteria will be considered.
Documents to Bring:
- Updated resume
- Aadhar copy
- Educational certificates
- Current CTC details
For any inquiries, feel free to reach out:
Email: hrd@supriyalifescience.com
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To apply for this job please visit supriyalifescience.com.