Head of Quality

Jchinteractivecoaching; London; Hybrid; GBP 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a Head of Quality to lead the Quality Assurance team in a dynamic and compliance-focused environment. This pivotal role involves overseeing compliance with GMP, GDP, and GPvP regulations, ensuring product quality and safety. The ideal candidate will have a strong background in quality leadership and regulatory affairs, with the ability to influence cross-functional teams and drive continuous improvement initiatives. If you are passionate about quality assurance and ready to make a significant impact in the pharmaceutical sector, this opportunity is for you.

Qualifications

• Strong knowledge of GDP, GMP, and GPvP in the pharmaceutical industry.
• Experience in leading quality teams with a proven track record in compliance.

Responsibilities

• Lead and develop the Quality Assurance team, ensuring compliance with GxP standards.
• Manage and enhance the Quality Management System and drive compliance initiatives.

Skills

Quality Assurance Leadership

Compliance Management

Risk Management

Analytical Skills

Communication Skills

Influencing Skills

Education

Degree in Life Sciences

Tools

eQMS

Job description

Join to apply for the Head of Quality role at JCH Interactive Coaching

Location: Central London | Hybrid/On-Site | Full-Time

We are looking for a Quality Assurance Lead to oversee compliance, risk management, and continuous improvement within our pharmaceutical operations. This role ensures that all GMP, GDP, and GPvP regulations are met while maintaining the highest standards of product quality and safety.

Key Responsibilities

Leadership & Compliance

• Lead and develop the Quality Assurance team, fostering a culture of accountability and excellence.
• Maintain compliance as a Manufacturing Authorisation Holder (MAH), ensuring adherence to all GxP standards.
• Oversee regulatory inspections, audits, and quality risk assessments, ensuring timely implementation of corrective and preventive actions (CAPAs).
• Act as the primary liaison with regulatory agencies and external stakeholders on quality matters.

Quality Management & Continuous Improvement

• Manage and enhance the Quality Management System (QMS), including the maintenance of SOPs, documentation, and QMS improvements.
• Implement risk assessments and mitigation strategies throughout the product lifecycle.
• Drive compliance initiatives through internal training, education, and process improvement programs.
• Monitor and report on quality metrics (KPIs), including deviation rates, CAPAs, and customer complaints.

Operational Oversight

• Ensure adherence to standard operating procedures in line with GMP, GDP, and GPvP practices.
• Manage product quality complaints, supplier qualifications, and technical agreements with third-party service providers.
• Support cross-functional teams, including supply chain, pharmacovigilance, regulatory affairs, and manufacturing, to align quality objectives.
• Ensure compliance with change controls, deviations, non-conformances, and internal audit observations.

About You

• Strong knowledge of GDP, GMP, and GPvP in the pharmaceutical industry.
• Experience in leading quality teams with a proven track record in compliance and regulatory affairs.
• Eligible or experienced Responsible Person (RP) and Responsible Person for Import (RPi).
• Familiarity with eQMS, risk management, CAPAs, and supplier oversight.
• Strong analytical, communication, and leadership skills with the ability to influence at all levels.
• Degree in Life Sciences or equivalent.

If you are a results-driven quality leader ready to take on a high-impact role in a fast-paced, compliance-driven environment, we would love to hear from you.

Apply now or reach out for a confidential discussion.

Seniority Level

Director

Employment Type

Full-time

Job Function

Manufacturing

Industries

Manufacturing