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B

Deputy Global Head of Quality

Barrington James Bishop's Stortford
new


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    B

    Deputy Global Head of Quality

    Barrington James Bishop's Stortford
    new
    Status Open
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    What we ask

    Education

    No minimum education required

    What we offer

    Salary

    Job description

    Deputy Global Head of Quality (Senior Consultant)

    Location: Bishop's Stortford, United Kingdom (Hybrid)

    Type: Permanent


    A growing international Regulatory, Compliance, and Product Development Consultancy is looking to appoint a Deputy Global Head of Quality to join its expanding global team.


    This is an excellent opportunity for an experienced GCP Quality professional looking to progress into a senior leadership role within a highly respected consultancy environment. The position offers exposure to a diverse portfolio of pharmaceutical, biotech, and clinical development projects across the UK, Europe, and internationally.


    Key Responsibilities:

    • Lead and oversee UK and EU Compliance Services activities

    • Conduct and manage GCP audits including clinical trial site audits, CRO audits, vendor audits, qualification audits, and system audits

    • Support regulatory inspection readiness activities and audit preparation

    • Lead CAPA management and issue resolution activities arising from audit findings

    • Perform QMS gap assessments and support the development of SOPs, policies, and quality documentation

    • Provide CRO oversight and sponsor support across clinical development programmes

    • Support the development and delivery of GCP training programmes

    • Contribute to global quality initiatives and continuous improvement activities

    • Mentor and support junior team members while helping shape the future growth of the quality function


    Requirements:

    • Degree qualified within a Life Science, Biomedical, or related scientific discipline

    • Minimum 5 years of hands-on GCP auditing experience

    • Strong experience conducting clinical trial, CRO, vendor, qualification, and system audits

    • Excellent knowledge of ICH-GCP and clinical trial compliance requirements

    • Experience supporting inspection readiness and regulatory audits

    • Experience managing CAPAs and quality improvement initiatives

    • Strong communication, stakeholder management, and leadership skills

    • Eligible to work in the UK without sponsorship

    • Willingness to travel throughout the UK, Europe, and occasionally internationally


    If you have a strong background in Clinical Quality Assurance and GCP Auditing and would be interested in discussing this opportunity further, please apply directly

    About the employer

    Barrington James
    Apply now

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    Apply now

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