Job Summary
Sex type: Both
Job Nature:Full Time
Age:Na
Experience:3 to 5 yearsThe applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies
Educational Requirements: Bachelor/HonorsMastersBachelor’s/ Master’s Degree in Pharmacy, Chemistry, Applied Chemistry from any reputed public/private university.
Salary Range: Negotiable
Published: 16 Sep 2026
Deadline: 10 Oct 2026
Vacancy: --
Job Description

Ziska Pharmaceuticals Limited, is one of the reputed pharmaceutical companies in Bangladesh. It is ISO 9001:2015 certified and has a fully GMP compliant factory which follows the USFDA guidelines. To support rapid expanding business, the company is looking for Sr. Officer, R & D Analytical.

Job Location:

  • Shofipur, Gazipur

Key Responsibilities:

  • To perform physical and chemical tests relevant to product development, analytical method development and validation of new and reformulated existing products.

  • To perform physical and chemical tests required for pre-formulation study by lab batch analysis of new and reformulated existing products.

  • To perform physical and chemical tests required for stability analysis such as accelerated stability, in use, real time or ongoing study of new and reformulated existing products.

  • To compile stability data for reformulated existing products based on accelerated stability, in use, real time or ongoing study.

  • To review & change implement of analytical methods and development procedure considering easiness, minimum consumption of reagent or solvent and reduction of cost.

  • To implement the procedures & Instructions of ISO -9001:2015 & 14001:2015 in own area of activity.

  • To undertake work related to specification change of development products and perform tests of incoming materials and products.

  • To ensure compliance of GLP at all stages of testing of products under product development programme.

  • To proof pharmaceutical equivalents following reverse engineering of Innovator/leader products along with generic products.

  • To prepare product STP (or revise in case of method, & product specification change) before technology transfer to validation department.

  • To perform works relevant to preparation and standardization of chemical reagents & working standard.

  • To implement GLP and ensure safe storage, distribution & disposition of reagents and chemicals.

  • Maintain records relevant to analysis, testing, batch processing etc. under product development.

  • Perform any other tasks assigned by Head of R & D/ Immediate Supervisor.

Job Requirements

3– 5 years of relevant experience in Pharmaceutical analytical R & D.Experience in handling analytical activities and product development and technology transfer will be preferred.Additional Requirements:Strong communication, collaboration skillsAnalytical Problem-solving and decision-making abilityIntegrity and continuous improvement mindsetMS Office and report preparationAbility to work under pressure and manage multiple operational requirements

Job Source

https://bdjobs.com/h/details/1534247

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