Supriya Lifescience Walk-In Drive Regulatory Affairs, R&D, QA, QC, and Production

Supriya Lifescience Limited, a public listed generic pharmaceutical company with USFDA and EUGMP approved facilities, is hosting a Walk-In Interview drive for multiple departments across its Ambernath and Goregaon locations.

The company is seeking experienced professionals for various roles essential to its API and Formulation (FDF) operations.

Walk-In Interview Details

Candidates interested in the Ambernath-based roles are requested to attend the walk-in.

Date: Saturday, 15th November 2025
Time: 9:00 am to 4:30 pm
Venue: Supriya Lifescience Ltd., Plot No. N-60, Additional Ambernath MIDC, Anand Nagar, Ambernath (East), Dist. Thane.
Can’t Attend? Email your CV/Resume to hrd@supriyalifescience.com.

Detailed Job Roles and Requirements

Department	Post	Qualification	Experience (Yrs)	Location	Key Responsibilities/Skills
Regulatory Affairs (RA)	Manager / Sr. Manager (US & Europe)	B.Pharm, M.Pharm	12 to 15	Goregaon	Develop and execute regulatory strategies for US (FDA) and EU markets (EMA). Lead preparation and submission of regulatory filings (NDA, MAA, variations) and manage agency communications.
FRD (Packaging)	Executive Packaging Development	B.Pharm/M.Pharm/BE/M.Sc with PG/PG diploma in Packaging research (IIP or equivalent).	7 to 10	Ambernath	Develop and validate primary, secondary, and tertiary packaging solutions compliant with GMP, FDA, EU. Conduct packaging testing and manage projects.
Quality Assurance (QA)	Sr. Officer / Executive	B.Pharm, M.Pharm	5 to 7	Ambernath	Qualification of process equipment, area, HVAC and Utility qualification. CSV validation (SIA, URS, DQ, IQ, OQ), and qualification of water systems.
Production	Manufacturing Executive / Sr.Executive (Injectable)	B.Pharm, M.Pharm	4 to 6	Ambernath	Planning, coordinating, and executing manufacturing operations (commissioning, qualification) as per cGMP. Ensures shift-wise production, compliance, and supports process validation/tech transfer.
FRD (OSD)	Research Scientist	B.Pharm, M.Pharm	3 to 5	Ambernath	Specializing in Solid Oral Dosage Forms (immediate, extended, delayed-release). Proficient in Quality by Design (QbD) principles and Process Development Report (PDR) preparation.
FRD (Injectable)	Research Scientist	B.Pharm, M.Pharm	3 to 5	Ambernath	Exposure to Injectable/OTF (Orally Thin Film) and Metered Dose Inhalation preferred. Proficient in Quality by Design (QbD) principles.
Quality Control (QC)	Officer / Sr. Officer	M.Sc, B.Pharm, M.Pharm	3 to 5	Ambernath	Water Sampling & Analysis, Raw/Packaging Material Sampling. Instrument Qualification (IQ, OQ, PQ, Calibration), QMS (Change Control, Incident, OOS), and Analytical Method Validation (AMV).
Production	Manufacturing Technician / Operator (Injectable/OSD)	12th/ITI/B.Sc	2 to 4	Ambernath	Operating Compression, Granulation, Liquid Filling, Vial Line, Autoclave, Visual Inspection, and Terminal Sterilizer machines. Includes Bin Washing and Solution Preparation.