At a Glance
- Tasks: Lead GCP compliance and conduct audits in a fast-paced life sciences consultancy.
- Company: Specialist life sciences consultancy with a focus on global regulatory expertise.
- Benefits: Competitive salary, professional development, and opportunities for international travel.
- Other info: Join a growing international team and contribute to continuous improvement.
- Why this job: Make a real impact in clinical trials while developing your leadership skills.
- Qualifications: Degree in life sciences and 5 years of GCP auditing experience required.
The predicted salary is between 60000 - 75000 £ per year.
A senior quality leadership position within a specialist life sciences consultancy delivering regulatory, clinical, and compliance expertise across global markets. The role focuses on GCP compliance, clinical trial oversight, and quality management system development within a fast-paced consulting environment. Working across UK and European projects, the position combines hands-on audit delivery with strategic quality leadership, supporting both client-facing work and internal quality initiatives within a growing international team.
RESPONSIBILITIES
- Lead UK and EU compliance service delivery, supporting wider global quality operations
- Plan, manage, and conduct GCP audits including vendor qualification, system audits, trial audits, and inspection readiness activities
- Own audit outcomes, driving structured issue resolution and corrective/preventive actions (CAPAs)
- Perform quality management system gap analyses and develop compliant documentation including SOPs and policies
- Provide sponsor oversight for clinical trials, acting as representative with CROs, sites, and vendors
- Deliver GCP training programmes tailored to client requirements
- Support development and execution of global quality assurance initiatives
- Maintain and improve quality management systems and associated processes
- Act as escalation point for complex quality and compliance issues across projects
- Ensure quality documentation, audit reports, training materials, and CAPAs are delivered to a high standard
- Contribute to continuous improvement and service excellence across client engagements
- Maintain billable utilisation through delivery of technical consulting work
REQUIREMENTS
- Degree in life sciences or related discipline (BSc essential; MSc or PhD preferred)
- Minimum 5 years’ experience in GCP auditing within clinical trials, vendors, systems, and inspection readiness environments
- Strong knowledge of ICH-GCP and regulatory compliance frameworks (GCP certification required)
- Proven experience writing SOPs and regulated quality documentation
- Experience in clinical trial oversight or sponsor-side quality assurance preferred
- Strong organisational and time management skills with ability to manage multiple priorities
- Demonstrated leadership or mentoring capability within technical teams
- Excellent communication, stakeholder management, and problem-solving skills
- Proficient in Microsoft Office and CRM systems
- Comfortable working autonomously and within international teams
- Willingness to travel within the UK, Europe, and occasionally internationally
To apply, submit your CV highlighting relevant experience. Applicants must be eligible to work in the UK without sponsorship requirements.
Quality Deputy Manager employer: Barrington James
As a leading specialist life sciences consultancy, we pride ourselves on fostering a dynamic and inclusive work culture that prioritises employee growth and development. Our Quality Deputy Manager role offers the opportunity to engage in impactful projects across the UK and Europe, while benefiting from comprehensive training programmes and a supportive international team environment. Join us to be part of a forward-thinking organisation that values quality excellence and innovation in the life sciences sector.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Deputy Manager
✨Tip Number 1
Network like a pro! Reach out to your connections in the life sciences field and let them know you're on the hunt for a Quality Deputy Manager role. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on GCP compliance and quality management systems. We recommend creating a list of common interview questions related to clinical trials and practice your responses. Confidence is key, so the more prepared you are, the better you'll perform!
✨Tip Number 3
Showcase your expertise! During interviews, be ready to discuss specific examples of your experience with GCP audits and quality documentation. Highlighting your past successes will help you stand out as a strong candidate for the role.
✨Tip Number 4
Don't forget to apply through our website! We make it easy for you to submit your CV and highlight your relevant experience. Plus, it shows you're genuinely interested in joining our team at StudySmarter!
We think you need these skills to ace Quality Deputy Manager
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Quality Deputy Manager role. Highlight your experience in GCP auditing and any relevant leadership roles you've held. We want to see how your background aligns with our needs!
Showcase Your Skills:Don’t just list your skills; demonstrate them! Use specific examples from your past work that showcase your organisational, problem-solving, and communication skills. This helps us see how you can contribute to our team.
Be Clear and Concise:When writing your application, keep it clear and to the point. We appreciate well-structured documents that are easy to read. Avoid jargon unless it's relevant to the role – we want to understand your experience without getting lost!
Apply Through Our Website:We encourage you to apply through our website for a smoother process. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at Barrington James
✨Know Your GCP Inside Out
Make sure you brush up on your knowledge of ICH-GCP and regulatory compliance frameworks. Be ready to discuss specific examples from your experience in GCP auditing, as this will show your depth of understanding and how you can apply it in real-world scenarios.
✨Showcase Your Leadership Skills
Since the role involves leading quality initiatives, prepare to share instances where you've demonstrated leadership or mentoring capabilities. Think about how you’ve guided teams through complex quality issues or improved processes, and be ready to discuss these experiences in detail.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills and ability to manage multiple priorities. Prepare some scenarios where you successfully resolved compliance issues or conducted audits, highlighting your structured approach to issue resolution and CAPAs.
✨Tailor Your Communication Style
Given the importance of stakeholder management in this role, practice articulating your thoughts clearly and concisely. Be prepared to discuss how you would deliver GCP training programmes tailored to client needs, showcasing your ability to adapt your communication style to different audiences.
