Nuvista Pharma Ltd.
Assistant Officer, Quality Control
General Info
- Published on: Apr 28, 2026
- Deadline: May 10, 2026
- Source: bdjobs
Job Details
- Job Nature: Full-Time
- Job Location: Gazipur
- Salary:
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Job Description:
- Perform routine analytical tests (e.g., HPLC, GC, UV-VIS) on raw materials, intermediates, and finished products to ensure quality compliance
- Manage the collection, labeling, storage, and documentation of samples, as well as the inventory of reagents and columns, ensuring proper usage and replenishment
- Assist senior QC personnel in organizing and compiling analytical data for regulatory documentation and filings
- Adhere to GMP and SOPs, supporting internal audits, CAPAs, and investigations to maintain high quality standards & regulatory compliance.
- Help maintain and calibrate QC lab equipment, ensuring proper functioning & troubleshooting any issues as they arise
Job Requirements
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Educational Requirements:
- Bachelor of Science (BSc) in Chemistry, Biochemistry
- Master of Science (MSc) in Chemistry, Biochemistry
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Experience Requirements:
- At most 2 years
- The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies
- Freshers are also encouraged to apply.
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Additional Requirements:
- At least 0 to 2 years working experience in any well-known pharmaceutical company
- Knowledge of cGMP regulations like USP/ВР, WHO, TGA, MHRA, US-FDA related to manufacturing of sterile and non-sterile pharmaceutical products is a plus
- Freshers are also encouraged to apply
Apply Procedure
- Apply Instructions: Interested candidates are requested to apply for the position. Only short listed candidates will be invited for further selection process.