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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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