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- Tasks: Lead the Quality function and ensure compliance in a biopharmaceutical setting.
- Company: Join a leading biopharmaceutical organisation in the South East of the UK.
- Benefits: Competitive salary, career advancement, and a strong quality culture.
- Other info: Equal Opportunities employer welcoming diverse applicants.
- Why this job: Make a real impact on quality governance and operational excellence.
- Qualifications: Degree in a scientific discipline and extensive biopharmaceutical experience required.
The predicted salary is between 80000 - 100000 £ per year.
We are currently looking for a Quality Director to join a leading biopharmaceutical organisation based in the South East of the UK. In this position, you will provide strategic leadership across Quality, ensuring robust governance, regulatory compliance and operational excellence across site activities. You will play a key role within the senior leadership team, supporting business performance and the ongoing development of a strong quality culture across the organisation.
Key Duties And Responsibilities
- You will lead and develop the Quality function, ensuring the team is structured, resourced and performing effectively to meet business and regulatory requirements.
- You will establish and evolve Quality strategy and systems, driving continuous improvement and alignment with wider organisational objectives.
- You will oversee compliance with GMP and applicable regulatory standards, maintaining a high level of inspection readiness and supporting external audits.
- As the Quality Director you will partner closely with cross functional teams to ensure quality is embedded across operational activities and decision making.
Role Requirements
- A Degree or higher level in a relevant scientific discipline (e.g., Biological Sciences / Pharmaceutical Sciences / Biotechnology) with extensive experience within the biopharmaceutical industry.
- Extensive experience working within regulated GMP environments, with strong understanding of Quality Systems and compliance frameworks. This should be from a Senior leadership standpoint.
- Proven experience leading and developing teams within a Quality function, with the ability to influence at senior levels.
- Demonstrated experience supporting regulatory inspections, audits and managing quality related risk within a complex environment.
Key Words
- Quality
- GMP
- GxP
- Quality Leadership
- Biopharmaceutical
- Compliance
- Regulatory
- QMS
- Audits
- CAPA
- Pharmaceutical
- Inspection Readiness
- Leadership
Quality Director employer: Hyper Recruitment Solutions
Contact Detail:
Hyper Recruitment Solutions Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Director
✨Tip Number 1
Network like a pro! Reach out to your connections in the biopharmaceutical industry and let them know you're on the lookout for a Quality Director role. You never know who might have the inside scoop on an opportunity or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GMP and regulatory compliance. Be ready to discuss how you've led teams and driven quality improvements in past roles. Show them you’re not just a fit for the job, but the perfect match!
✨Tip Number 3
Don’t forget to showcase your leadership skills! When chatting with potential employers, highlight your experience in developing quality functions and influencing senior management. They want to see that you can lead and inspire a team towards operational excellence.
✨Tip Number 4
Apply through our website! We’ve got loads of opportunities waiting for you, and applying directly can give you a better chance of standing out. Plus, it shows you’re serious about joining the team and making a difference in the quality landscape.
We think you need these skills to ace Quality Director
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Quality Director role. Highlight your experience in GMP environments and any leadership roles you've held. We want to see how your background aligns with our needs!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality in the biopharmaceutical industry and how you can contribute to our quality culture. Keep it engaging and relevant!
Showcase Your Achievements: Don’t just list your responsibilities; showcase your achievements! Use specific examples of how you've driven continuous improvement or led successful audits. We love to see results that speak for themselves.
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It helps us keep track of your application and ensures you don’t miss out on any important updates from us!
How to prepare for a job interview at Hyper Recruitment Solutions
✨Know Your Quality Systems
Make sure you brush up on your knowledge of Quality Systems and compliance frameworks. Be ready to discuss how you've implemented these in previous roles, especially in GMP environments. This will show that you understand the core of what the role entails.
✨Showcase Your Leadership Skills
Prepare examples that highlight your experience in leading and developing teams within a Quality function. Think about specific challenges you've faced and how you influenced senior stakeholders to achieve quality objectives. This will demonstrate your capability as a strategic leader.
✨Be Audit-Ready
Since the role involves supporting regulatory inspections and audits, be prepared to talk about your experiences with these processes. Share how you maintained inspection readiness and managed quality-related risks in complex environments. This will illustrate your hands-on experience.
✨Align with Organisational Objectives
Understand the company's mission and values, and think about how your vision for Quality aligns with their organisational objectives. Be ready to discuss how you would drive continuous improvement and embed quality across operational activities, showcasing your strategic thinking.