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Research Laboratory Jobs at USV Ltd | M.Pharm, M.Sc

USV Pvt. Ltd is 58 year old leading healthcare company which began as a joint venture with USV&P Inc. USA, a subsidiary of Revlon. Our product offering today includes Active Pharmaceutical Ingredients (APIs), Fixed Dosages Formulations (FDF), Peptides, Biosimilars and Injectables. These are manufactured in our cGMP compliant plants located in India.

Analytical Research Laboratory (Position Code: ARL1)
Location : Govandi (Mumbai)
Position : Research Analyst / Sr. Research Analyst (Multiple Vacancies)
Experience : 2+ years
Qualification : M.Sc (Chemistry)
Job profile :
• Method development/ Method optimization
• Method Validation/ Verification/ Comparison
• Routine Analysis
• cGMP related documentation
Other details :
Candidates should have exposure of regulatory audits like USFDA, MHRA etc.

Interested applicants may send their resumes to

Drug Delivery and Research Laboratory (Position Code: DDRL1 )
Location : Govandi (Mumbai)
Position : Research Pharmacist
Experience : 2+ years
Qualification : M. Pharm
Position Code : DDRL

Job profile :
Formulation development of modified / immediate release dosage forms for Regulated Markets.
Technology transfer to manufacturing location.

Documentation-review of PDR, QOS, Batch documents like BMR, Process validation protocol, Cleaning validation protocol, etc.
Other details :
Candidates should have exposure of regulatory audits like USFDA, MHRA etc. Exposure to the QBD methodology and experience in Solid orals or Parenterals will be highly preferred.

Interested applicants may send their resumes to

Biologics Research Laboratory – Quality Assurance (Position Code: BRL1)
Location : Nerul (Navi Mumbai)
Position : Officer / Executive / Sr. Executive
Experience : 2+ years
Qualification : Graduate or Post Graduate in Biotechnology / Biochemistry / Microbiology / Chemistry / Pharmacy.
Job profile :
Knowledge of validating processes like fermentation, purification using chromatography techniques etc.

Well versed with line clearances, issuance & retrievals of documents.
IPQA monitoring of the processes and reporting deviations and non-compliance’s
Reviewing of batch records, clean utilities and coordinating for internal audits.
Cleaning validations, CIP and SIP validations etc.
Experience in failure investigations, in-process data reviews and qualifications of process equipments
Other details :
Candidates should have experience of GMP.

Interested applicants may send their resumes to

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