Research & Development (Analytical) Professional at Aristopharma Ltd – Gazipur

Active

Analytical Chemistry, Biotechnology

Gazipur

Full Time

Any

Vacancy 1 position

Salary & vacancy

1 vacancy

Job Description

Aristopharma Ltd is seeking a motivated Research & Development (Analytical) Professional to join its Gazipur laboratory. This full‑time, office‑based role involves preparing and reviewing source‑approval documents, AMV protocols, specifications, SOPs and justifications to satisfy US‑FDA, TGA, UK‑MHRA and EU market requirements. The successful candidate will execute analytical method validations, verifications and transfers according to ICH Q2(R2) guidelines, conduct reverse engineering of product formulations, and perform ophthalmic product analysis, especially dissolution and particle‑size determination of suspensions.

The position demands strict adherence to quality systems, including change control, incident handling, deviations, CAPA and QMS management. Candidates will operate and maintain key analytical instruments such as ICP, GC, HPLC and UV, performing troubleshooting, installation, qualification and calibration tasks. This role offers a valuable entry‑level opportunity for individuals interested in pharmaceutical R&D, analytical chemistry and regulatory compliance, with the potential to grow within Aristopharma’s dynamic environment.

Requirements

Education Requirements

Educational background is not specified.

Experience Requirements

Experience level is entry‑level; no minimum years required.

Qualifications

Key professional qualifications expected for this position include:

Understanding of ICH Q2(R2) guidelines and cGMP/GLP principles
Familiarity with US‑FDA, TGA, UK‑MHRA, EU regulatory requirements
Ability to prepare and review technical documents such as AMV protocols, specifications, SOPs and justifications

Skill Requirements

Operation and maintenance of ICP, GC, HPLC, UV instruments
Analytical method validation, verification and transfer
Reverse engineering of product formulations
Dissolution and particle size analysis of ophthalmic suspensions
Change control, incident, deviation and CAPA management
Documentation compliance with EP/BP/USP standards

Incentive & compensation

No incentive or bonus details were provided.

How to apply for Aristopharma Ltd jobs

Follow these steps to submit your application:

Click the external application link: https://forms.gle/pa35ne5mV5NbD5xN8
Complete the online form with your up‑to‑date CV and any supporting documents.
Submit the form before the application deadline (if any) as indicated on the form.

About Aristopharma Ltd

Aristopharma Ltd is a leading pharmaceutical manufacturer in Bangladesh, dedicated to developing high‑quality medicines for domestic and international markets. With a strong focus on research, development and regulatory compliance, the company offers career opportunities that contribute to innovative healthcare solutions.