Head of QC

Overview
A well‑established pharmaceutical manufacturer is seeking an experienced Quality Control (QC) Head to oversee laboratory operations, uphold product quality standards, and ensure full compliance with regulatory and GMP requirements. This role is responsible for safeguarding analytical integrity, driving continuous improvement, and leading QC teams toward operational excellence.

Key Responsibilities
• Lead and oversee the QC department
Manage analysts, microbiologists, and technicians, ensuring smooth operations and alignment with quality objectives.

• Oversee analytical testing activities
Supervise testing for raw materials, in‑process samples, finished goods, and stability studies, ensuring accurate and validated results.

• Approve batch release decisions
Review documentation and analytical outcomes to authorize product batches in compliance with established specifications and SOPs.

• Ensure regulatory and GMP compliance
Maintain compliance with cGMP, cGLP, and PIC/S requirements while reinforcing data integrity and laboratory discipline.

• Develop QC procedures and validation programs
Create, revise, and implement SOPs, analytical methods, and validation protocols to maintain reliable laboratory performance.

• Manage laboratory quality systems
Oversee deviations, CAPA, OOS/OOT investigations, change controls, and documentation systems to ensure continuous compliance.

• Coordinate audits and continuous improvement efforts
Prepare QC teams for regulatory and supplier audits, while driving improvements in testing efficiency, cost control, and method robustness.

Key Qualifications & Requirements
• Relevant tertiary qualifications
Bachelor’s or Master’s degree in Pharmacy, Chemistry, Pharmaceutical Science, or a related discipline.• Extensive QC leadership experience
Minimum 15 years in pharmaceutical QC with at least 5 years in a managerial capacity.

• Strong technical and regulatory expertise
Proficiency in GMP/GLP, stability testing, analytical techniques (HPLC, GC, UV, titration), and microbiology testing.

• Experience in investigations and validations
Demonstrated ability to manage OOS/OOT, method validation and transfer, and regulatory inspection readiness.

• Strong leadership and communication skills
Ability to lead teams effectively, resolve problems, communicate clearly, and work with laboratory information systems and presentation tools.

Why Join This Organization
You will take on a critical leadership role within a reputable and stable pharmaceutical manufacturer, influencing quality strategy and contributing to the production of safe, high‑quality healthcare products. This position offers opportunities for professional growth, technological exposure, and the ability to shape laboratory excellence and quality culture.