Senior Officer, R & D Analytical
Job Description
Title: Senior Officer, R & D Analytical
Company Name: Ziska Pharmaceuticals Ltd.
Vacancy: --
Age: At least 27 years
Job Location: Anywhere in Bangladesh
Salary: Negotiable
Experience:
- 3 to 5 years
- The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies
Published: 2026-09-16
Application Deadline: 2026-10-10
Education:
- Bachelor/Honors
- Masters
Bachelor’s/ Master’s Degree in Pharmacy, Chemistry, Applied Chemistry from any reputed public/private university.
Requirements:
- 3 to 5 years
- The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies
Skills Required:
Additional Requirements:
- Age At least 27 years
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 skills
Analytical Problem-solving and decision-making ability
Integrity and continuous improvement mindset
MS Office and report preparation
Ability to work under pressure and manage multiple operational requirements
Responsibilities & Context:
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 Other Benifits:
Salary: Negotiable, based on experience and qualifications
Three Festival Bonuses yearly
Contributory Provident Find
Gratuity
Profit Sharing (WPPF)
Group Insurance
Mobile Phone Allowance
Employment Status: Full Time
Job Work Place:
Company Information:
Gender: Both Male and Female can apply
Read Before Apply: Please apply only who are fulfilling all the requirements of this job
Category: Pharmaceutical
