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Assistant Officer, Quality Control
Nuvista Pharma PLC
Gazipur
Full TimeNot specifiedBdJobsActive Hiring
Salary
Negotiable
Deadline
9 May 2026
Source
BdJobs
Location
Gazipur
72%
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Salary
Negotiable
Deadline
9 May 2026
Key Responsibilities
* Drive quality compliance by conducting routine analytical tests, including HPLC, GC, and UV-VIS, on raw materials, intermediates, and finished products
* Oversee sample management, including collection, labeling, storage, and documentation, as well as reagent and column inventory, to ensure efficient usage and replenishment
* Collaborate with senior QC personnel to architect and compile analytical data for regulatory submissions and documentation
* Champion GMP and SOP adherence, supporting internal audits, CAPAs, and investigations to uphold high quality standards and regulatory compliance
* Manage and maintain QC lab equipment, performing calibrations and troubleshooting issues to ensure optimal functionality and minimize downtime
Requirements
Experience
At most 2 years
Education
- Bachelor of Science (BSc) in Chemistry, Biochemistry
- Master of Science (MSc) in Chemistry, Biochemistry
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
Compensation & Benefits
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