Company Name: General Pharmaceuticals Ltd

Roles & Responsibilities:

• Prepare product dossier in CTD, ACTD and country specific for regulatory submission of different export countries.
• On time response of all queries from regulatory agencies after submission of dossier.
• Review technical documents and perform any changes required.
• Perform any other projects assigned by department head regarding QA regulatory issues.
• Perform sampling and in-process check (IPC) during manufacturing of ophthalmic, injectable and oral solid products.
• Prepare, review and update documents in accordance to WHO-GMP, EU-GMP, PIC/S-GMP on time.
• Prepare & submit reports time to time as per requirement of department head

Educational Qualification:

• M. Pharm from any reputed public and private university

Work Experience:

• At most 2 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