Manager QA – Pharmaceutical Laboratory (Pharm D Required)

Job Overview

We are hiring a Manager QA (Pharm D) to lead the Quality Assurance function in our pharmaceutical laboratory. This role is dedicated to ensuring process compliance, regulatory adherence, and GMP standards, without involvement in QC activities. The candidate will oversee QA systems, documentation, audits, and compliance processes to ensure that medicines are consistently manufactured to the highest standards.

Key Responsibilities

• Establish, implement, and monitor Quality Assurance systems in line with GMP and regulatory requirements.
• Ensure compliance across manufacturing, packaging, storage, and distribution processes.
• Lead and manage deviation investigations, change control, product recalls, and complaints handling.
• Review and approve Batch Manufacturing Records (BMRs), SOPs, and QMS documentation.
• Manage CAPA (Corrective & Preventive Actions) and ensure timely closure with follow-up.
• Conduct internal GMP audits and self-inspections to assess system effectiveness.
• Develop and deliver QA training programs for staff to strengthen compliance culture.
• Ensure proper documentation, traceability, and reporting for all QA-related activities.
• Collaborate with cross-functional teams to ensure continuous quality improvement.

Key Skills

• Strong knowledge of QA processes specific to pharmaceuticals.
• Excellent understanding of GMP, QMS, SOPs, and regulatory compliance.
• Strong leadership, documentation, and analytical skills.
• High attention to detail and ability to enforce compliance.

Qualifications & Experience

• Pharm D (Doctor of Pharmacy) – mandatory
• Minimum 3 years of proven experience in a QA managerial role in the pharmaceutical industry.
• In-depth knowledge of GMP and QA systems (no QC responsibilities).
• Preference for male candidates due to operational requirements in the laboratory.

Job Type: Full-time

Pay: Rs150,000.00 per month

Application Question(s):

• Explain your experience in Quality Assurance within the pharmaceutical industry. Include your total years of QA experience and the areas you have worked in (e.g., manufacturing, packaging, documentation, audits).

Work Location: In person