Job Description / Responsibility
- Analysis of drug substance & drug product.
- Analytical method development and preparation of STP.
- New source approval related activities for raw material & packaging material.
- Handling of analytical instruments like HPLC, GC, AAS, UV-VIS, FTIR, LC-MS Dissolution tester, Karl fisher apparatus, Autotitrator, Disintegration tester etc.
- Analysis of prototype, scale up, exhibit batch of new product.
- Analytical method validation, report preparation.
- Stability Study and preparation of Stability Study Report.
- Preparation of making working plan and report.
- Preparation of Product Dossier and other relevant regulatory documents.
Job Nature
Full-time
Educational Requirements
- M. Pharm or M.Sc in Chemistry/ Biochemistry/ Applied Chemistry from reputed university with excellent academic record.
Job Requirements
- 1 (one) year(s) experience on analytical section of R & D department or Quality Control department in a reputed pharmaceuticals company is preferable.
- Knowledge on GMP, GLP, Calibration, Validation, Drug Rules & Regulations.
- Knowledge on FDA and ICH guideline.
- Ability to work under pressure.
- Computer literacy.
- Strong communication skill.
Job Location
Gazipur
Apply Instruction:
Applicant must enclose his/her Photograph with CV.
Application Deadline : Nov 12, 2016
Job Source
Bdjobs.com Online Job Posting
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