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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 environment.
- Why this job: Make a real impact by driving operational excellence and fostering a culture of continuous improvement.
- Qualifications: 7+ years in quality assurance or manufacturing, with knowledge of ISO, FDA, and cGMP standards.
- Other info: This is a key leadership role with the chance to shape quality strategies.
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.
- Lead the development and execution of site quality strategies, ensuring compliance with industry regulations.
- 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.
7+ years' experience in quality assurance or manufacturing operations, ideally within regulated industries (e.g., Life Sciences, Biotech, Medical Devices).
In-depth knowledge of quality standards and regulations (ISO, FDA, cGMP).
Proven track record in driving process improvements and ensuring regulatory compliance.
Director, Data Quality employer: EPM Scientific
Contact Detail:
EPM Scientific Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Director, Data 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 quality standards and regulations mentioned in the job description, such as ISO, FDA, and cGMP. Consider obtaining certifications or attending workshops that focus on these areas to demonstrate your commitment and expertise.
✨Tip Number 3
Prepare to discuss your previous experiences in leading quality teams and driving process improvements. Be ready to share specific examples of how you've successfully implemented quality management systems and aligned them with business goals in past roles.
✨Tip Number 4
Research StudySmarter's current quality initiatives and values. Understanding our company culture and how we approach quality management will help you tailor your conversations and show how you can contribute to our mission.
We think you need these skills to ace Director, Data Quality
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in quality assurance and manufacturing operations. Emphasise your leadership roles and any specific achievements related to regulatory compliance and process improvements.
Craft a Compelling Cover Letter: In your cover letter, clearly articulate your understanding of the role and how your background aligns with the company's needs. Mention your experience with quality management systems and your approach to fostering a culture of continuous improvement.
Highlight Relevant Experience: When detailing your work history, focus on your 7+ years of experience in regulated industries. Include specific examples of how you've managed audits, quality metrics, and compliance reporting to demonstrate your expertise.
Showcase Leadership Skills: Since this is a key leadership role, be sure to highlight your ability to lead high-performing teams. Discuss your strategies for aligning quality initiatives with business goals and driving operational excellence.
How to prepare for a job interview at EPM Scientific
✨Showcase Your Leadership Skills
As a Director of Site Quality, you'll be leading a team. Be prepared to discuss your leadership style and provide examples of how you've successfully managed teams in the past, particularly in quality assurance or regulated industries.
✨Demonstrate Regulatory Knowledge
Familiarise yourself with key regulations such as ISO, FDA, and cGMP. Be ready to discuss how you have ensured compliance in previous roles and how you would approach regulatory challenges in this position.
✨Highlight Process Improvement Experience
Prepare to share specific examples of process improvements you've implemented in your past roles. Discuss the impact these changes had on quality metrics and overall operational excellence.
✨Align Quality Initiatives with Business Goals
Understand the company's business objectives and think about how quality initiatives can support these goals. Be ready to discuss how you would partner with senior leadership to align quality strategies with broader business aims.
