Executive Analytical Development

Year    Vadodara, Gujarat, India

Job Description


List of Responsibilities / Job function:

  • 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 & In process Material.
  • Responsible for method Validation studies of API & In process Material.
  • Responsible for stability studies of API & In process Material.
  • 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.

Sun Pharmaceutical Industries

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Job Detail

  • Job Id
    JD3199454
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    Vadodara, Gujarat, India
  • Education
    Not mentioned
  • Experience
    Year