Company Name: General Pharmaceuticals Ltd.

Roles & Responsibilities:

• Perform analysis, documentation and review data of finished products of solid dosage form.
• Performa analytical activities of process validation & optimization of solid dosage form.
• Perform sampling and testing (Identification, Physicochemical tests, impurity and assay) of raw materials.
• Handling of Out of Specification (OOS)/ Out of Trend (OOT), LIR, Deviation related to solid dosage form and raw materials.
• Prepare SOP/ESP and others QC related documents on time.
• Perform all test relevant to cleaning validation and submit report on it.
• Perform any other project assigned by department head.

Educational Qualification:

• M. Pharm/ M.Sc. in Chemistry/ Applied Chemistry/ Bio-Chemistry from any reputed public and private university.

Work Experience:

• At least 3 year(s)
• The applicants should have experience in the following area(s):

  Others Requirements:

  • Process Oriented
  • Cost Efficiency
  • Drive for Results
  • Flexibility
  • Compliance
  • KPI Driven
  • Computer Literacy

  Others Benefit:

  Provident fund, Gratuity Lunch Facilities: Partially Subsidize Salary Review: Yearly Festival Bonus: 2 Others benefits as per company policy.

   

  Source: Bdjob