Job Description
Title: Executive - Quality Assurance
Company Name: DBL Pharmaceuticals Ltd.
Vacancy: --
Location: Gazipur
Experience:
∎ At most 1 year
∎ The applicants should have experience in the following business area(s):Pharmaceutical/Medicine Companies
∎ Freshers are also encouraged to apply.
Published: 21 May 2025
Education:
∎ Master of Pharmacy (M.Pharm) in Pharmacy
Requirements:
Additional Requirements:
∎ Advanced knowledge in MS Suite will be preferred;
∎ Strong decision-making skills with the ability to work independently and collaboratively;
∎ Strong interpersonal skill to deal with internal & external stakeholders.
∎ Advanced knowledge in MS Suite will be preferred;
∎ Strong decision-making skills with the ability to work independently and collaboratively;
∎ Strong interpersonal skill to deal with internal & external stakeholders.
Responsibilities & Context:
∎ Perform In-Process Control (IPC) activities during manufacturing in compliance with cGMP guidelines;
∎ Conduct line clearance at all production stages including Dispensing, Granulation, Packaging etc;
∎ Sample intermediates, granules, bulk and finished products across production stages;
∎ Prepare and maintain Quality-related SOPs and relevant documentation;
∎ Inspect finished products and review batch records for accuracy and compliance;
∎ Manage documentation issuance, control, retrieval and archiving per regulatory standards;
∎ Maintain IPC instrument logbooks;
∎ Compile batch data and assist in preparing Annual Product Quality Review (APQR) reports;
∎ Participate in validation, qualification and toll manufacturing activities;
∎ Handle deviations, CAPA, change control and market complaints;
∎ Oversee batch release processes and ensure timely compliance;
∎ Manage specification updates and sample approvals in ERP (Oracle).
∎ Perform In-Process Control (IPC) activities during manufacturing in compliance with cGMP guidelines;
∎ Conduct line clearance at all production stages including Dispensing, Granulation, Packaging etc;
∎ Sample intermediates, granules, bulk and finished products across production stages;
∎ Prepare and maintain Quality-related SOPs and relevant documentation;
∎ Inspect finished products and review batch records for accuracy and compliance;
∎ Manage documentation issuance, control, retrieval and archiving per regulatory standards;
∎ Maintain IPC instrument logbooks;
∎ Compile batch data and assist in preparing Annual Product Quality Review (APQR) reports;
∎ Participate in validation, qualification and toll manufacturing activities;
∎ Handle deviations, CAPA, change control and market complaints;
∎ Oversee batch release processes and ensure timely compliance;
∎ Manage specification updates and sample approvals in ERP (Oracle).
Workplace:
∎ Work at office
Employment Status: Full Time
Job Location: Gazipur
Company Information:
∎ DBL Pharmaceuticals Ltd.
Read Before Apply: Please apply only who are fulfilling all the requirements of this job
Application Deadline: 9 Jun 2025
Category: Others
