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- Tasks: Lead quality management initiatives and ensure compliance with industry regulations.
- Company: Join a dynamic team in Devon focused on quality assurance in regulated industries.
- Benefits: Enjoy competitive salary, career growth opportunities, and a supportive work culture.
- Why this job: Make a real impact by driving operational excellence and fostering continuous improvement.
- Qualifications: 7+ years in quality assurance or manufacturing, with strong leadership skills required.
- Other info: Ideal for those passionate about quality in Life Sciences, Biotech, or Medical Devices.
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 Life Sciences and Biotech sectors. Attend industry conferences or local meetups to connect with individuals who may have insights into the role or even know about openings at StudySmarter.
✨Tip Number 2
Research the latest trends and regulations in quality assurance, particularly those related to ISO, FDA, and cGMP. Being well-versed in current standards will not only boost your confidence but also demonstrate your commitment to the field during discussions.
✨Tip Number 3
Prepare to discuss your leadership style and experiences in managing high-performing teams. Think of specific examples where you successfully implemented quality initiatives or drove process improvements, as these will be crucial in showcasing your fit for the role.
✨Tip Number 4
Familiarise yourself with StudySmarter's mission and values. Understanding our culture and how we align quality initiatives with business goals will help you articulate how you can contribute to our success during any interviews.
We think you need these skills to ace Director Site Quality
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in quality assurance and leadership. Focus on your achievements in regulated industries, particularly those that align with the job description.
Craft a Compelling Cover Letter: Write a cover letter that specifically addresses the key responsibilities mentioned in the job description. Use examples from your past experiences to demonstrate how you have successfully led quality management initiatives.
Highlight Regulatory Knowledge: Emphasise your understanding of industry regulations such as ISO, FDA, and cGMP in both your CV and cover letter. This will show that you are well-versed in the compliance aspects crucial for the role.
Showcase Leadership Skills: Provide specific examples of how you have developed and managed high-performing teams. Mention any initiatives you led that resulted in process improvements or operational excellence.
How to prepare for a job interview at EPM Scientific
✨Showcase Your Leadership Experience
As a Director of Site Quality, strong leadership skills are crucial. Be prepared to discuss specific examples of how you've successfully led teams in the past, particularly in regulated industries. Highlight your ability to foster a culture of continuous improvement.
✨Demonstrate Knowledge of Regulatory Standards
Make sure you have a solid understanding of quality standards and regulations such as ISO, FDA, and cGMP. During the interview, be ready to explain how you've applied these standards in your previous roles and how you plan to ensure compliance in this position.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your problem-solving skills and decision-making abilities. Think about challenges you've faced in quality management and how you overcame them, especially in relation to audits and compliance reporting.
✨Align Quality Initiatives with Business Goals
Be prepared to discuss how you would partner with senior leadership to align quality initiatives with broader business objectives. Show that you understand the importance of integrating quality management into the overall operational strategy.
