QA Manager

Job Description

Title: QA Manager

Company Name: M/s Super Power Pharmaceuticals Ltd.

Vacancy: 02

Age: 35 to 50 years

Job Location: Narsingdi (Belabo)

Salary: Negotiable

Experience:

• At least 6 years
• The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies

• Master of Pharmacy (M.Pharm)

• Candidate must have computer skill & well conversant with Microsoft Office applications.

• Candidate should have registration number given by Bangladesh Pharmacy Council.

• At least 6 years
• The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies

• Age 35 to 50 years

Candidate should have profound knowledge on Standard Operating Procedure (SOP), Pharmaceutical Analysis, Pharmaceutical Calibration/Validation, Process Validation, Proper Documentations, Regulatory Affairs etc. Candidate should be skilled on HPLC, FTIR, UV, ASS, GC, TLC & others QC Equipment’s. Enable to prepare MOA, COA, Method Verifications and Specifications, Method Validations. Coordinate pharmaceutical-related activities for all products.

• Write, review, implement & maintain a Quality Management System (QMS) (i.e. Deviation, Investigation, risk assessment, change control, CAPA, customer complaint, Product recall, Internal audit, Personnel Training etc.)

• Support regulatory inspections and compliance audits.

• Design, implement, and update the quality manuals, policies, and systems in strict compliance with current Good Manufacturing Practices (cGMP), ICH guidelines, and global regulatory frameworks.

• Oversee the drafting, reviewing, updating, and approval of all critical SOPs across departments to ensure operational standardization.

• Ensure the manufacturing facility is continuously ready for external inspections by organization like dgda.

• Schedule and conduct regular internal audits across various departments (Production, QC, Engineering) to proactively catch and fix gaps.

• Direct the investigation into any manufacturing deviations, Out-Of-Specification (OOS) lab results, or process anomalies to establish the true root cause.

• Challenge, approve, and track Corrective and Preventive Actions (CAPAs) to ensure systemic flaws are permanently fixed rather than relying on surface-level patches.

• Review and approve changes to facility structures, manufacturing equipment, raw materials, or software systems, minimizing unexpected risks to product quality.

• Conduct the comprehensive final review of batch manufacturing records (BMR) and batch packaging records (BPR) to verify compliance before market release.

• Define, evaluate, and govern recurring GMP and compliance training programs across the entire workforce.

• Perform Annual Product Quality Review (APQR) of finished products.

• Conduct testing of raw materials, in-process, and finished products.

• Perform stability studies and ensure analytical method validation.

• Maintain laboratory compliance with safety and GLP standards.

• Collaborate with production and R&D for troubleshooting quality issues.

• Perform any other duties assigned by management as required.

• Salary Review: Yearly
• Festival Bonus: 2

• Salary & other benefits will be considered as per company rules & policies.

• Special preference will be given to the candidates who have practical knowledge & experience in launching injectable/Sterile Products and attractive salary will be offered to such candidates.