Nuvista Pharma Limited
Nuvista Pharma Limited
Nuvista Pharma Limited
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Summary
- Vacancy: —
- Location: Gazipur (Tongi)
- Experience: 1 to 3 years
- Published: 27 Jul 2024
Requirements
Education
- M. Pharm or M.Sc. in Chemistry / Biochemistry from any reputed University.
Experience
- 1 to 3 years
- Freshers are also encouraged to apply.
Additional Requirements
- At least 1 to 3 years working experience in a well-known pharmaceutical Quality Control laboratory is preferred.
- Knowledge of cGMP regulations like USP/BP, WHO, TGA, MHRA, US-FDA related to manufacturing of sterile and non- sterile pharmaceutical products is a plus.
Responsibilities & Context
- Analytical work (i.e. raw material, intermediate, bulk, packing material, finished product and stability studies) of products according to the specified method and routine chemical analysis of PW, WFI and PS.
- Preparation of RM and finished product specification, COA, testing method, SOPs and register.
- Perform analysis of cleaning validation, process validation & method validation of products.
- Monitoring of calibration, qualication & maintenance of QC equipment and their proper documentation.
- Ensuring that raw materials, components, products, or monitoring results that do not meet specications or expectations are promptly investigated, risk assessed and necessary CAPAs are implemented.
Employment Status
Full Time
Job Location
Gazipur (Tongi)