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Head of Quality/RPi

JR United Kingdom

London

On-site

GBP 60,000 - 100,000

Full time

7 days ago
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Job summary

An established industry player in medical aesthetics is seeking a Head of Quality to ensure compliance with regulatory frameworks and oversee quality assurance activities. This pivotal role involves maintaining the Quality Management System, leading audits, and mentoring the QA team. The ideal candidate will have over 10 years of experience in a senior QA role, a degree in pharmacy or life sciences, and a strong understanding of global supply chain regulations. If you are passionate about quality assurance and compliance in a dynamic environment, this is the perfect opportunity to make a significant impact.

Qualifications

  • 10+ years in senior QA roles, strong knowledge of regulatory frameworks.
  • Proven leadership in QA strategy and compliance.

Responsibilities

  • Oversee medicines licenses and ensure compliance with regulations.
  • Maintain the Quality Management System and lead audits.

Skills

Leadership
Analytical Skills
Problem-Solving
Communication
Regulatory Compliance
Quality Assurance

Education

Degree in Pharmacy
Degree in Life Sciences

Tools

Quality Management System (QMS)

Job description

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A leading supplier of medical aesthetic products and services, supporting professionals across the UK and Ireland. The company partners with well-known brands to bring high-quality products to market, serving thousands of clinics with a comprehensive range of skincare, injectables, medical devices, and supporting services. With a strong focus on innovation and compliance, the company offers a dynamic environment for career growth.

About the Role

We are seeking a highly skilled and experienced professional to join our team as Head of Quality (QA). This individual will act as the Responsible Person (RP/RPi) on our Wholesale Dealers Authorisation (WDA) and Quality Controller (QC) on our Manufacturer’s Specials (MS) Authorisation. The successful candidate will ensure that all operations meet or exceed Good Distribution & Manufacturing Practices (GMDP) in line with regulatory requirements.

Responsibilities

  • Oversee the company’s medicines licenses, including WDA(h) & MS licenses.
  • Develop and implement strategies to ensure compliance with wholesale and import regulations for medicines, medical devices, and cosmetic products.
  • Report key compliance issues directly to senior leadership.
  • Maintain the Quality Management System (QMS), including document control, change control, validation, deviation management, CAPA programs, complaint handling, and SOP oversight.
  • Lead internal and external audits, mitigating risks in operations.
  • Provide QA guidance and training across internal teams, ensuring alignment with industry regulations.
  • Develop QA KPIs to track quality performance and improvements.
  • Collaborate with external industry bodies to stay ahead of regulatory changes.
  • Act as the primary contact for regulatory agencies and external audits.
  • Mentor and develop the QA and Regulatory Team, fostering a high-performance culture.
  • Approve marketing materials related to medicines and medical devices.

Additional Requirements

  • Flexibility to travel between company facilities.
  • Strong understanding of global supply chain regulations, particularly post-Brexit.

Candidate Profile

  • Degree in pharmacy, life sciences, or related field.
  • 10+ years’ experience in a senior QA role within a global supply chain.
  • Strong knowledge of MHRA, FDA, HPRA (preferred), GDP, GMP, and GxP regulatory frameworks.
  • Proven leadership experience in QA strategy, compliance, and continuous improvement programs.
  • Strong analytical and problem-solving abilities.
  • Excellent communication, leadership, and mentoring skills.
  • Previous experience managing a QMS in a global supply chain environment.
  • Familiarity with aesthetic medicine products is highly desirable.
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