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Manager, Quality Assurance (QA)

Alkad Laboratories, Rangpur
Rangpur Healthcare/Medical Full Time Office At least 10 years Not disclosed 1 vacancy Posted Jun 10, 2026 Deadline Jun 30, 2026

Job Description

Job Context: Alkad Laboratories is looking for a dynamic, detail-oriented, and experienced professional to lead our Quality Assurance department. The successful candidate will oversee the implementation of GMP standards, manage controlled documentation, and ensure rigorous data integrity across all functional areas of the plant.

Job Responsibilities

  • Quality Management Leadership: Manage the full lifecycle—including approval, implementation, and monitoring—of all official logbooks and controlled documents. Ensure strict documentation standards are maintained across all operational areas, including Manufacturing, QC, QA, Engineering, Warehouse, and Administration.

  • SOP & Documentation Control: Authorize, review, and approve the requisition, technical issuance, and implementation of departmental logbooks and Standard Operating Procedures (SOPs).

  • Training & Qualification: Oversee and mandate rigorous training programs for all managers and officers regarding documentation handling, ensuring no unauthorized personnel issue or sign off on critical records.

  • Cross-Functional Coordination: Collaborate directly with Production, Product Development, Microbiology, Quality Control, and Engineering heads to review request forms, follow up on implementations, and manage regular self-inspections.

  • Audits and Archiving: Direct the secure, systematic, long-term archiving of completed corporate records and logbooks for technical inspection readiness.

Experience

  • At least 10 years
  • The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies, Medical Equipment

Education

    • Master of Pharmacy (M.Pharm)

Additional Requirements

  • Age At least 40 years

Experience: Minimum 10 years of active experience in the Quality Assurance department of a reputed pharmaceutical industry.

Core Competencies:

  • In-depth understanding of Good Manufacturing Practices (GMP) and regulatory guidelines.

  • Strong expertise in controlled document lifecycle management (SOPs, EOPs, ECPs).

  • Proven experience executing technical reviews and maintaining rigorous data integrity systems.

  • Excellent leadership, cross-departmental coordination, and training delivery skills.

Skills & Expertise

Quality assurance and control

Compensation & Other Benefits

    • Salary: Negotiable (Based on experience and competence)

    • Benefits: As per company policy (e.g., Festival Bonuses, and other standard industrial benefits).

How to Apply

If you meet the requirements and want to grow your career with Alkad Laboratories, please apply through  this Email: alkadlab@gmail.comNote: Only short-listed candidates will be called for an interview.

Send your CV to the given email alkadlab@gmail.com or Email your CV from My Bdjobs account