No. of Vacancies
Job Description / Responsibility
- To develop analytical Method & Validation
- To analysis of Raw materials specially INN material
- To analysis of Trial product
- To participate on stability study of Lab batches & Process Validation batches (Accelerated & long term)
- To work on Documentation (Analysis report, Stability report, Analytical Method Validation Report etc.)
- M. Pharm (Preferably from Public University)
- 4 to 6 year(s)
- The applicants should have experience in the following area(s):
Quality Controller /Assurance, Research, Production
- The applicants should have experience in the following business area(s):
Additional Job Requirements
- Age 28 to 33 year(s)
- Having experience on Analytical section of R&D department or Quality Control department in a reputed Pharmaceutical company.
- Candidate must be capable for Analytical Method Development & Validation and expert on HPLC, UV, Atomic absorption spectroscopy, GC & IR operation.
- As per company policy
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Application Deadline : May 2, 2016