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Department: Biologics Research Laboratory – Quality Assurance (Position Code: BRL1)


Department: Biologics Research Laboratory – Quality Assurance (Position Code: BRL1) Login before Share This Job
USV Private Limited
hrd@usv.in
Mumbai
Pharma / Biotech
Admin
23 Jan 2018

Opportunities

  1. Department: 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 deepti.joshi@usv.in

  2. Department: 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 reena.bhole@usv.in

  3. Department: 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 kajal.bhanushali@usv.in

CONTACT

Tel: +91-22-2556-4048 & 6786-1111

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