Manager, QA
Job Description
Title: Manager, QA
Company Name: Nipa Pharmaceuticals Ltd.
Vacancy: --
Age: 40 to 55 years
Job Location: Dhaka
Salary: Negotiable
Experience:
- 10 to 15 years
- The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies
Published: 2026-06-21
Application Deadline: 2026-07-21
Education:
- Master of Pharmacy (M.Pharm)
Requirements:
- 10 to 15 years
- The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies
Skills Required: Computer Literacy,Quality Assurance,Quality Inspection,Quality Management System
Additional Requirements:
- Age 40 to 55 years
Responsibilities & Context:
Organize and carryout analytical activities of raw materials, packing materials and finished products and to ensure quality of product by implementing guidelines of WHO, ICH, FDA, TGA, etc.
Perform in process Checking, BMR, BPR and SOP�s preparation and checking during manufacturing of products.
Participate in all qualification and validation activities.
Ensure proper documentation of all quality assurance related documents.
Ensure other activities like environment control, water sanitation, waste disposal, HVAC system validation, and ETP, housekeeping, health & personnel hygiene.
Ensure required Training of QA/Production/Engineering/Ware house personnel.
Maintain all Compliance related activities and documentation.
Would be a plus if familiar with dossier preparation for International market and other export related work.
Responsible for all In Process Quality Assurance activities (IPQA) on the shop floor including quality oversight and Batch record review.
Responsible to perform SAP (SHAPE) activities in the QM Module and will be the part of Deviation Management, investigation of market complains and other compliance activities.
Sampling & Analysis of Raw Materials, Packaging Materials, Finished Products and Water.
Handling of all sophisticated QC instruments like HPLC, GC, UV-VIS, FTIR, TOC, Dissolution tester, Karl fisher autotitrator & Disintegration tester etc.
Preparation and review of SOPs, specifications & methods for raw material, packaging material & finished product etc.
Validation of analytical methods, Cleaning & Qualification of equipments.
Preparation & standardization of volumetric solution, secondary working standards from reference standard etc.
Calibration of all sophisticated QC equipments.
Handling of OOS with proper investigation.
Maintain GLP & housekeeping and make corrective measures for any deviation.
Job Other Benifits:
Employment Status: Full Time
Job Work Place: Work at office
Company Information:
Gender: Male and Female can apply
Read Before Apply: Please apply only who are fulfilling all the requirements of this job
Category: Pharmaceutical
