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For Companies At a Glance
- Tasks: Lead quality management initiatives and ensure compliance with industry regulations.
- Company: Join a leading firm in the Life Sciences and Biotech sector, focused on innovation.
- Benefits: Enjoy a full-time role with opportunities for professional growth and development.
- Why this job: Make a real impact by driving quality excellence and fostering a culture of improvement.
- Qualifications: 7+ years in quality assurance, strong leadership skills, and knowledge of ISO, FDA standards.
- Other info: This is a key leadership role based in beautiful Devon.
The predicted salary is between 54000 - 84000 £ per year.
We are seeking a Director of Site Quality to lead and drive quality management initiatives in Devon. This is a key leadership role focused on ensuring compliance with regulatory standards and overseeing the implementation of best practices in quality assurance.
Key Responsibilities:
- Lead the development and execution of site quality strategies, ensuring compliance with industry regulations (e.g., ISO, FDA, cGMP).
- Manage and optimise the Quality Management System (QMS) across the site.
- Lead a high-performing quality team, fostering a culture of continuous improvement.
- Partner with senior leadership to align quality initiatives with business goals and drive operational excellence.
- Oversee internal and external audits, quality metrics, and compliance reporting.
Who You Are:
- 7+ years' experience in quality assurance or manufacturing operations, ideally within regulated industries (e.g., Life Sciences, Biotech, Medical Devices).
- Strong leadership skills with experience in managing and developing high-performing teams.
- In-depth knowledge of quality standards and regulations (ISO, FDA, cGMP).
- Proven track record in driving process improvements and ensuring regulatory compliance.
Director Site Quality employer: EPM Scientific
Contact Detail:
EPM Scientific Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Director Site Quality
✨Tip Number 1
Network with professionals in the quality assurance field, especially those who have experience in regulated industries like Life Sciences or Biotech. Attend industry conferences or local meetups to connect with potential colleagues and learn about the latest trends and challenges in quality management.
✨Tip Number 2
Familiarise yourself with the specific regulatory standards relevant to the role, such as ISO, FDA, and cGMP. Consider obtaining certifications or attending workshops that focus on these regulations to demonstrate your commitment and expertise in quality assurance.
✨Tip Number 3
Prepare to discuss your leadership style and experiences in managing high-performing teams. Think of specific examples where you successfully led a team through quality improvements or compliance challenges, as this will showcase your ability to align quality initiatives with business goals.
✨Tip Number 4
Research StudySmarter's values and mission to understand how they align with your own professional philosophy. Be ready to articulate how your vision for quality management can contribute to their goals, which will help you stand out as a candidate who is not only qualified but also a good cultural fit.
We think you need these skills to ace Director Site Quality
Some tips for your application 🫡
Understand the Role: Thoroughly read the job description for the Director of Site Quality position. Make sure you understand the key responsibilities and required qualifications, as this will help you tailor your application.
Highlight Relevant Experience: In your CV and cover letter, emphasise your 7+ years of experience in quality assurance or manufacturing operations. Provide specific examples of how you've managed teams and driven process improvements in regulated industries.
Showcase Leadership Skills: Demonstrate your leadership abilities by including examples of how you've developed high-performing teams and fostered a culture of continuous improvement. Use metrics or outcomes to illustrate your impact.
Tailor Your Application: Customise your CV and cover letter to align with the company's values and the specific requirements of the role. Mention your knowledge of quality standards and regulations like ISO, FDA, and cGMP to show you're a perfect fit.
How to prepare for a job interview at EPM Scientific
✨Showcase Your Leadership Experience
As a Director of Site Quality, your leadership skills are crucial. Be prepared to discuss specific examples of how you've successfully managed and developed high-performing teams in the past.
✨Demonstrate Regulatory Knowledge
Familiarise yourself with the relevant regulations such as ISO, FDA, and cGMP. During the interview, highlight your experience in ensuring compliance and how you have navigated regulatory challenges in previous roles.
✨Discuss Quality Management Systems
Be ready to talk about your experience with Quality Management Systems (QMS). Share insights on how you've optimised QMS processes and the impact it had on operational excellence at your previous workplaces.
✨Align Quality Initiatives with Business Goals
Prepare to explain how you have partnered with senior leadership to align quality initiatives with broader business objectives. This shows your understanding of the strategic importance of quality in driving overall success.
