Quality Assurance In-Charge (Pharmaceutical Industry)

Max Pharmaceuticals is looking for a highly skilled and experienced Quality Assurance Manager to join our team. The successful candidate will have extensive knowledge of pharmaceutical quality systems and a strong background in Quality Control. This role requires a professional who can ensure compliance with regulatory standards while effectively managing quality assurance activities within the organization.

Key Responsibilities
- Oversee and manage all Quality Assurance activities to ensure adherence to GMP, GLP, SOPs, and regulatory requirements.
- Handle batch release processes, deviation investigations, CAPA implementation, change control, and maintain accurate documentation.
- Monitor in-process controls, finished product quality, and laboratory operations to maintain high standards.
- Coordinate closely with Production, Quality Control, and Regulatory Affairs departments to streamline quality processes.
- Lead and supervise the QA team, ensuring compliance with company policies and regulatory guidelines.
- Drive continuous improvement initiatives to enhance quality systems and operational efficiency.

Required Qualifications
- A Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, or a related field.
- A minimum of 10 years of professional experience in the pharmaceutical industry, with at least 5 years of hands-on experience in Quality Control.
- Strong knowledge of GMP, GLP, SOPs, and regulatory compliance requirements.
- Proven experience in batch release, deviation handling, CAPA, change control, and documentation management.
- Excellent leadership and coordination skills to work effectively across multiple departments.

Additional Information
The position is based at the National Industrial Zone, Rawat, Islamabad. The role requires in-person attendance with working hours from 8:00 AM to 5:00 PM, Monday through Saturday, with only the first Saturday of each month off. The monthly salary range for this position is Rs. 100,000 to Rs. 170,000.

Interested candidates who meet the above criteria are encouraged to apply by submitting their updated CV, clearly indicating the position title. This is an excellent opportunity for a dedicated professional to contribute to a growing pharmaceutical company committed to quality and compliance.