VCARE Biolabs, a rapidly growing Contract Research and Development Organization established with a focus on integrity, quality, safety, customer satisfaction, and principles. We provide end to end solutions to Bio-pharma, Vaccine and Pharmaceutical industries by delivering products of the highest quality with global, standards,

Analytical Research & Development (1-6 yrs)

Qualification: M.Sc, B.Pharmacy, M. Pharmacy

Experience in method development, validation, routine analysis, documentation, regulatory support. Exposure in handling instrurnents like HPLC, UV, IR etc.,

Downstream: Purification (1-6 yrs)

Qualification: M.Sc, B.Pharmacy, M. Pharmacy

  • • Protein purification, Chromatography, AKTA process, TFF and Ultra filtration.The person should have knowledge 65 66515 Practices.
    • Hands on experience in Microbial/ Cell culture process development for Biosimilars.
    • Single use Chrornatography and protein purification operation and process development at large scale.
    • Regulatory compliance documentation .
    • Technology transfer

Molecular Biologist (1-6 yrs)

Qualification: M.Sc, B.Pharmacy, M.Pharmacy

  • Experence in cloning, plasmid isolation, PCR, Expression studies
  • Platforms: E.coli, Yeast , mammalian cell culture

Formulation R&D (1-6 yrs)

Qualification: M.Sc, B.Pharmacy, M.Pharrnacy

  • Should have experence in development of tablets, injections, oncology and non-oncology products

Upstream: Fermentation (1-6 yrs)

Qualification: M.Sc, B.Pharmacy, M.Pharrnacy

  • Expert in handling of SCADA associated fermenters, TFF system and mobile/product storage vessels Able to trouble shoot the equipment’s such as fermentor and TFF system 
  • Experience with media preparation activities
  • Knowledge in QMS Activities The individual needs to communicate within the organization and be able to work within a team as well as independently.

Regulatory Affairs (1-6 yrs)

Qualification: M.Sc, B.Pharmacy, M.Pharrnacy

  • To review the Document requirernents for Registration and check availability of documents as per Registration request Provide Request to relevant departments for required documents and take tirnely follow ups to accomplish documentation within tirnelines.
  • Collection of Regulatory registration related documents from relevant departrnents, review and their cornpilation for preparation of final dossier.
  • Prepare Registration dossiers to meet the timelines and dispatch the documen. to relevant countries as and when required by custorners after confirmation Work on the queries raised by customer/ Regulatory authorities of country of registration for the submitted documents and resolve with necessary documentation as and when required.
  • Review and analyze scientific and medical documentation, research and locate information on regulatory requirements of similar products
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