Manager, R & D Analytical
Job Description
Title: Manager, R & D Analytical
Company Name: Ziska Pharmaceuticals Ltd.
Vacancy: --
Age: At least 34 years
Job Location: Gazipur
Salary: Negotiable
Experience:
- 10 to 12 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:
- 10 to 12 years
- The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies
Skills Required:
Additional Requirements:
- Age At least 34 years
10-12 years of relevant experience in Pharmaceutical analytical R & D.
Experience in handling analytical activities for new product development and reformulation will be preferred.
Additional Requirements:
Strong communication, coordination and follow-up skills
Problem-solving and decision-making ability
Leadership, ownership and accountability
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 Manager, R & D (Analytical).
Job Location:
Shofipur, Gazipur
Key Responsibilities:
To Plan, Coordinate, review and oversee physical and chemical testing related to new product development and reformulation of existing products.
To conduct analytical testing required for pre-formulation studies and laboratory batch evaluation of new and reformulated products.
To develop, review, optimize and revise analytical methods and procedures considering accuracy, reliability, ease of execution, minimum consumption of reagents/solvents, laboratory safety and cost effectiveness.
To conduct accelerated, real-time, ongoing and in-use stability studies of new and reformulated products as per approved protocols and ensure timely analysis and evaluation of stability data.
To compile, analyze and interpret stability data and provide technical recommendations regarding product stability, trends, specifications and product development decisions.
To perform comparative analysis of innovator/leader products and own products during product development and stability studies and undertake testing of incoming materials and development batches as required.
To prepare, review and revise Standard Testing Procedures (STPs), analytical specifications and related documents and ensure their readiness for technology transfer to the validation/concerned department.
To ensure compliance with GLP and applicable quality requirements at all stages of analytical activities and implement relevant procedures and instructions of ISO 9001:2015 and ISO 14001:2015 within the area of responsibility.
To prepare, standardize and manage chemical reagents and working standards and ensure their proper documentation, safe storage, distribution, usage and disposition in accordance with established procedures.
To maintain accurate and complete records and documentation related to analytical testing, method development, stability studies, batch analysis, reagents, working standards and other product development activities while ensuring data integrity and traceability.
To provide technical guidance and coordinate analytical R&D activities with Formulation R&D, QA, QC, Validation, Production and other relevant functions, identify opportunities for continuous improvement and cost optimization.
To coordinate day-to-day analytical activities with R & D Executives and ensures effective utilization of laboratory resources.
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
• Other fringe benefits as per policy
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
