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- Tasks: Lead quality assurance in a dynamic biotech, ensuring compliance and driving improvements.
- Company: Join an innovative biotech firm focused on groundbreaking cancer treatments.
- Benefits: Enjoy hybrid working, competitive salary, bonuses, healthcare, and 25 days holiday.
- Why this job: Be part of a family-friendly culture that values well-being and growth.
- Qualifications: Degree in Biological Sciences; senior QA experience in pharma or biotech required.
- Other info: Open to various UK locations; thrive in a fast-paced, collaborative environment.
The predicted salary is between 72000 - 84000 £ per year.
Founding Director, Carrot Recruitment, Pharma & Life Sciences Specialists
Clinical Quality Assurance Director – Innovative and fast-growing biotech – Cambridgeshire or Cheshire with hybrid working (open to other UK locations) – £excellent basic salary, 20-30% bonus, pension, healthcare, life assurance, death in service, 25 days holiday + BH
The Company
• Innovative biotech moving into pivotal trials for promising drug targeting specific cancers
• Fast-growing and ambitious yet realistic with future growth plans
• Very flexible, agile organisation
• Family friendly company who genuinely value employee well-being
The Role
• Establish and embed robust quality management procedures
• Develop and implement GCP quality systems aligned with relevant standards (ICH, FDA, EMA).
• Provide QA oversight, coordinate and implement audit plans for CROs & GCP vendors
• Ensure inspection readiness and host GCP inspections (FDA, EMA, MHRA).
• Drive continuous improvement in quality systems and compliance strategies.
You
• Degree in Biological Sciences or a related field (advanced degree preferred).
• Experienced in a senior, hands-on Quality role within the pharmaceutical or biotech industry.
• Strong expertise in GCP regulations and clinical development.
• Experience working with CROs.
• Experience leading/hosting US and international health authority inspections.
• Ability to thrive in a fast-paced, collaborative environment.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Quality Assurance
Industries
Pharmaceutical Manufacturing and Biotechnology Research
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Clinical Quality Assurance Director employer: Carrot Recruitment
Contact Detail:
Carrot Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Quality Assurance Director
✨Tip Number 1
Network with professionals in the biotech and pharmaceutical industries. Attend relevant conferences or webinars where you can meet people who work in quality assurance roles. This can help you gain insights into the company culture and potentially get a referral.
✨Tip Number 2
Familiarise yourself with the latest GCP regulations and quality management systems. Being well-versed in current standards will not only boost your confidence but also demonstrate your commitment to the role during interviews.
✨Tip Number 3
Prepare to discuss specific examples of how you've driven continuous improvement in quality systems in your previous roles. Use the STAR method (Situation, Task, Action, Result) to structure your responses effectively.
✨Tip Number 4
Research the company’s recent projects and their approach to drug development. Understanding their pipeline and challenges will allow you to tailor your discussions and show how your experience aligns with their goals.
We think you need these skills to ace Clinical Quality Assurance Director
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in Quality Assurance within the pharmaceutical or biotech industry. Emphasise your expertise in GCP regulations and any relevant leadership roles you've held.
Craft a Compelling Cover Letter: Write a cover letter that specifically addresses the requirements of the Clinical Quality Assurance Director role. Mention your experience with CROs, your ability to lead inspections, and how you can contribute to the company's growth and quality management procedures.
Showcase Relevant Achievements: In both your CV and cover letter, include specific examples of how you've driven continuous improvement in quality systems or successfully managed audits. Quantify your achievements where possible to demonstrate your impact.
Proofread and Edit: Before submitting your application, carefully proofread your documents for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a role in Quality Assurance.
How to prepare for a job interview at Carrot Recruitment
✨Know Your GCP Regulations
Make sure you have a solid understanding of Good Clinical Practice (GCP) regulations. Be prepared to discuss how you've implemented these standards in your previous roles, as this will demonstrate your expertise and readiness for the position.
✨Showcase Your Leadership Experience
Since the role involves leading QA oversight and hosting inspections, highlight your leadership experience. Share specific examples of how you've successfully managed teams or projects, particularly in high-pressure situations.
✨Familiarise Yourself with the Company
Research the biotech company thoroughly. Understand their products, mission, and recent developments. This knowledge will help you tailor your responses and show genuine interest in their work during the interview.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your problem-solving skills and ability to handle compliance issues. Think of past experiences where you faced challenges and how you overcame them, as this will showcase your critical thinking and adaptability.
