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- Tasks: Lead quality and regulatory strategies for medical devices and pharmaceuticals.
- Company: Proclinical is a dynamic company focused on healthcare compliance and quality improvement.
- Benefits: Enjoy a culture of continuous improvement and professional growth opportunities.
- Why this job: Join us to make a real impact in the healthcare industry while developing your expertise.
- Qualifications: In-depth knowledge of UK regulations; additional qualifications in regulatory affairs are a plus.
- Other info: Be part of a team that values quality-first approaches and proactive problem-solving.
The predicted salary is between 43200 - 72000 £ per year.
Proclinical is seeking a Quality and Regulatory Lead to guide and implement regulatory and quality strategies. The successful candidate will work with pharmaceuticals, medical devices, and nutraceuticals regulatory frameworks, ensuring compliance and fostering a culture of continuous improvement.
Develop and execute UK regulatory and quality strategies aligned with business goals.
Promote a quality-first culture and continuous improvement.
Provide quality and compliance consultancy to senior management.
Anticipate regulatory changes to identify growth opportunities.
Manage UK regulatory activities, including product registration and compliance.
Ensure MHRA inspection readiness and manage audits.
Lead the quality plan for local product portfolios.
Oversee quality management systems and ensure data integrity.
Address product quality issues and manage local recalls.
Problem-solving skills in regulatory issues.
In-depth knowledge of UK regulations for drugs, medical devices, and nutraceuticals.
additional qualifications in regulatory affairs are beneficial.
Quality Director Medical Devices employer: Proclinical Staffing
Contact Detail:
Proclinical Staffing Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Director Medical Devices
✨Tip Number 1
Familiarize yourself with the latest UK regulations for medical devices and pharmaceuticals. Understanding the nuances of these regulations will not only help you in interviews but also demonstrate your commitment to compliance and quality.
✨Tip Number 2
Network with professionals in the quality and regulatory field. Attend industry conferences or webinars to connect with others who are already in similar roles. This can provide valuable insights and potentially lead to referrals.
✨Tip Number 3
Stay updated on recent changes in regulatory frameworks and quality management systems. Being able to discuss recent developments during your conversations with us will show that you are proactive and knowledgeable.
✨Tip Number 4
Prepare to discuss specific examples of how you've fostered a quality-first culture in previous roles. Highlighting your problem-solving skills and experience with audits will set you apart as a candidate who can lead our quality initiatives effectively.
We think you need these skills to ace Quality Director Medical Devices
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Quality Director position. Understand the key responsibilities and required qualifications, especially regarding regulatory frameworks and quality management systems.
Highlight Relevant Experience: In your CV and cover letter, emphasize your experience with pharmaceuticals, medical devices, and nutraceuticals. Provide specific examples of how you've implemented quality strategies or managed compliance in previous roles.
Showcase Problem-Solving Skills: Demonstrate your problem-solving abilities in regulatory issues. Include examples where you successfully navigated complex regulatory challenges or improved quality processes.
Tailor Your Application: Customize your application materials to reflect the company's focus on a quality-first culture and continuous improvement. Use language from the job description to align your application with their values and goals.
How to prepare for a job interview at Proclinical Staffing
✨Show Your Regulatory Expertise
Make sure to highlight your in-depth knowledge of UK regulations for drugs, medical devices, and nutraceuticals. Be prepared to discuss specific regulatory frameworks you've worked with and how you've ensured compliance in previous roles.
✨Demonstrate Problem-Solving Skills
Prepare examples of how you've successfully navigated regulatory challenges in the past. Discuss your approach to problem-solving and how you anticipate regulatory changes to identify growth opportunities.
✨Promote a Quality-First Culture
Be ready to talk about how you've fostered a culture of continuous improvement in your previous positions. Share specific initiatives you've led that promoted quality and compliance within your teams.
✨Prepare for Audit Scenarios
Since managing audits and ensuring MHRA inspection readiness is crucial, think of scenarios where you've successfully managed audits or inspections. Discuss your strategies for maintaining data integrity and addressing product quality issues.
