Job Description / Responsibility
- Sampling & Analysis of Raw Materials, Packaging Materials, Finished Products and Water.
- Handling of all sophisticated QC instruments like HPLC, UV-VIS, FTIR, TOC, Dissolution tester, Karl fisher autotitrator & Disintegration tester etc.
- Preparation & standardization of volumetric solution, secondary working standards etc..
- Preparation and review of SOPs, specifications & methods for raw material, packaging material & finished product etc.
- Validation of analytical methods & Qualification of equipments.
- Perform IPC activities in every steps of manufacturing and implement cGMP regulations.
- Preparation of export related documents as per country wise requirement.
Job Nature
Full-time
Educational Requirements
- M. Pharm from any recognized university.
Experience Requirements
- 1 to 2 year(s)
Additional Job Requirements
- Age 24 to 30 year(s)
- 2-3 year(s) working experience in QA department at any reputed pharmaceutical company will be given preference.
- Well conversant with MS-Office
- Good Communication skill
Job Location
Comilla
Salary Range
Negotiable
Other Benefits
- As per company policy.
Apply Instruction:
Applicant must enclose his/her Photograph with CV.
Application Deadline : Aug 8, 2016
Job Source
Bdjobs.com Online Job Posting
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