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SUN PHARMA

Executive - Analytical Development

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  • Posted 2 months ago
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Job Description

  • To work as per cGMP and ensure its compliance as per current guideline and SOPs.
  • Responsible to take training before execution of allotted work & maintaining the training file.
  • Responsible to follow safety precaution as per laboratory procedure.
  • Responsible to escalate any issue / incident to reporting manager for prompt corrective action.
  • Responsible for method development studies of API, Drug Product & In process Material preferably Peptide molecules
  • Responsible for method Validation studies of API, Drug Product & In process Material preferably Peptide molecules
  • Responsible for routine and stability studies of API, Drug Product & In process Material preferably Peptide molecules
  • Responsible to perform the pharmacopeial evaluation study as per requirement.
  • Responsible to align with organization goal.
  • Other responsibilities assigned by reporting authority.
  • Responsible to follow Quality Management Document procedure.
  • Responsible to perform the calibration of instrument.
  • Responsible to prepare Study Protocol and Study Reports.
  • Responsible to maintain instrument/equipment as per SOPs.
  • Responsible for timely archival of documents as per SOP.
  • Responsible to follow safety precaution as per laboratory procedure.
  • Responsible to ensure proper Handling and Disposal of waste.
  • Responsible to qualification reference standard / working standard/chemical reference standard samples as per approved and valid procedure.

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Job ID: 141072963

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