At a Glance
- Tasks: Lead quality compliance activities and conduct GCP audits across diverse projects.
- Company: A respected international consultancy in regulatory and product development.
- Benefits: Hybrid working, competitive salary, and opportunities for professional growth.
- Other info: Mentorship opportunities and involvement in global quality initiatives.
- Why this job: Step into a senior leadership role and shape the future of quality in healthcare.
- Qualifications: Degree in Life Science and 5+ years of GCP auditing experience required.
The predicted salary is between 63000 - 77000 £ per year.
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
Deputy Global Head of Quality employer: Barrington James
Barrington James is an exceptional employer that fosters a collaborative and innovative work culture, making it an ideal place for professionals in Epidemiology and Real-World Evidence. With a strong emphasis on employee growth, we offer tailored development opportunities and the chance to lead impactful projects across diverse therapeutic areas in the dynamic UK/Europe market. Join us to be part of a team that values flexibility, creativity, and meaningful contributions to healthcare advancements.
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We think this is how you could land Deputy Global Head of Quality
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We think you need these skills to ace Deputy Global Head of Quality
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Barrington James!
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How to prepare for a job interview at Barrington James
✨Understand the Science
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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
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In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
