Sr. Executive, Microbiology

Job Description

Title: Sr. Executive, Microbiology

Company Name: Nipa Pharmaceuticals Ltd.

Vacancy: --

Age: Na

Job Location: Dhaka

Salary: Negotiable

Experience: --

Published: 2026-02-01

Application Deadline: 2026-03-03

Education:

Requirements: --

Skills Required:

Additional Requirements:

Responsibilities & Context:

• Perform sampling and microbial testing of Raw Materials, finished products, water and ETP as per written procedure.

• Identify and isolate pathogenic microorganism in solvents & products.

• Perform settle plate count in dispensing, processing and primary packaging areas.

• Determine total coliforms in water.

• Perform bioload tests in clean areas.

• Perform IPC activities in every step of manufacturing and implement cGMP regulations.

• Preparation and updating of SOPs, specifications and methods for raw material, water and finished products etc.

• Prepare SOP for all instruments of Microbiology Department.

• Perform the operation, Qualification, Calibration and Validation of microbiological instruments.

• Prepare and preserve media as per compendia.

• Perform Environment monitoring as per requirement.

• Monitor, control & maintain records of hygiene for Microbiology, Warehouse & Production Department.

• Review, evaluate and make recommendations regarding microbiological hazards on manufacturing facilities, processes,

• equipment, packing, testing laboratories, materials, that have impact on microbial quality of pharmaceuticals.

• Neutralize antimicrobial properties in products.

• Perform sterility tests by both membrane filtration and direct inoculation method.

• Perform microbial limit tests.

• Perform microbial tests and release from user end point for production.

• Establish microbial alert and action level within process and product specifications.

• Perform antimicrobial effectiveness testing.

• Perform colony count tests.

• Perform BIOASSAYS.

• Determine whether enforcement actions and compliance policies incorporate sound scientific and technical information.

• Train Production, Housekeeping and Warehouse people with respect to microbiological point of view.

• Review and evaluate regulatory action submission focusing on Good Manufacturing Practice (GMP) violations.

• Evaluate evidence and inspection narratives to determine microbial risks.

• Check sterile production areas daily.

• Check all people in Production area daily with respect to microbiological point of view.

• Incorporate fundamental knowledge of the intended use of a product when evaluating risks, based on understanding of the patient populations taking a drug and their susceptibility to infection.

• Apply new developments and theories to novel problems or potential public health threats for which guidance does not currently exist.

• Meet with stakeholders to exchange information and to provide advice and guidance.