Assistant Manager/Deputy Manager - QA
Job Description
Title: Assistant Manager/Deputy Manager - QA
Company Name: Veritas Pharmaceuticals Ltd.
Vacancy: 1
Age: 35 to 42 years
Job Location: Gazipur
Salary: Negotiable
Experience:
- 8 to 10 years
- The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies
Published: 2026-04-05
Application Deadline: 2026-04-12
Education:
- Master of Pharmacy (M.Pharm)
Requirements:
- 8 to 10 years
- The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies
Skills Required:
Additional Requirements:
- Age 35 to 42 years
- Only Male
Responsibilities & Context:
Implementation of quality policy along with the quality Management system for improvement of product quality & Services.
Continual improvement of Quality Management system.
Monitoring of process product quality.
Responsible for final Batch Release as a QP (Qualified person)
Monitor all operations that affect quality
To be Responsible for Determining, negotiating and agreeing on in-house quality procedures, standards and specifications.
Be responsible for updates and share of the GMP and GLP requirements.
Setting customer service standard.
Specifying quality requirements of raw materials with suppliers & Approval of Vendor.
Investigating and setting standards for quality, health and safety.
Interaction with all departments for improving the product quality and process with the analysis of defects.
Be responsible for approval of written procedures and other documents including amendments.
To be responsible for supervision of validation and validation related activities as well as the approval of validation documents.
To be responsible of release of final batch (Finished Product) with the certification of Batch confirmation as a Qualified Person (QP).
Determination of training need based on the evaluation. Approval of training records and assessor of trainer.
To implement the applicable documented quality Management System procedures.
Be responsible for approval of specification of Raw, Packaging & Finished Product.
Approval of samples and pharmaceuticals documents for registration of products.
Be Responsible for approval of Dossiers & other Regulatory documents.
Be responsible for the handling & approval of deviation, CAPA and market complaint.
Be responsible of implementation of Quality Risk Management with approval of QRM documents.
Ensure the quality control and microbiological activities.
Coordination of Management review meeting and supervision of proposed action plan.
Job Other Benifits:
- Lunch Facilities: Full Subsidize
- Salary Review: Yearly
- Festival Bonus: 2
Employment Status: Full Time
Job Work Place:
Company Information:
Gender: Only Male can apply
Read Before Apply: Please apply only who are fulfilling all the requirements of this job
Category: Pharmaceutical
