Home / Job / USV LIMITED – Openings for Analytical Research Laboratory / Drug Delivery & Research Laboratory / Biologics Research Laboratory – QA

USV LIMITED – Openings for Analytical Research Laboratory / Drug Delivery & Research Laboratory / Biologics Research Laboratory – QA

USV LIMITED – Openings for Analytical Research Laboratory / Drug Delivery & Research Laboratory / Biologics Research Laboratory – QA

 

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

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

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

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About Pharmaceutical Guidanace

Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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