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- Tasks: Provide technical support and manage quality systems in medical device manufacturing.
- Company: Join a leading multinational company with over 50 years of expertise in high precision equipment.
- Benefits: Enjoy flexible working, competitive salary, bonuses, and excellent benefits.
- Why this job: Be part of an expert team making a real impact in the medical sector.
- Qualifications: Proven experience in quality assurance and regulatory affairs within medical devices required.
- Other info: Opportunity to conduct audits and resolve quality issues in a dynamic environment.
The predicted salary is between 36000 - 60000 £ per year.
An excellent role on offer for an individual with quality assurance and regulatory experience within the medical sector looking to play a key role at an industry leading company.
Do you have quality assurance and regulatory affairs experience within the medical devices sector? Would you like to work for a world leading company? Established for over 50 years, this multi-national company specialise in the design and manufacture of high precision equipment used within a range of industries. They have gone from strength to strength in recent years and are now looking for a Quality Assurance & Regulatory Affairs Officer to join their expert team.
In this role you will be tasked with providing technical support and guidance for medical device manufacturing, engineering and distribution. This will require you to oversee all quality assurance, regulatory compliance and quality systems within the business. You will also be tasked with carrying out audits and resolving quality issues. This role would therefore suit an individual with proven quality assurance and regulatory experience within the medical sector who is looking for a new challenge and the chance to play a key role at an industry leading company.
The Role:
- Technical support and guidance for manufacturing
- Managing quality systems
- Conducting audits
- Managing all relevant documentation
Salary: DOE + Bonus + Flexible Working + Excellent Benefits
The Person:
- Proven quality assurance and regulatory experience
- Experience with medical devices
- Strong understanding of relevant quality and regulatory requirements
Quality Assurance & Regulatory Affairs Officer employer: TN United Kingdom
Contact Detail:
TN United Kingdom Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance & Regulatory Affairs Officer
✨Tip Number 1
Network with professionals in the medical devices sector. Attend industry conferences or webinars to meet people who work in quality assurance and regulatory affairs. This can help you gain insights into the role and potentially lead to referrals.
✨Tip Number 2
Familiarise yourself with the latest regulations and standards in the medical device industry. Being knowledgeable about ISO standards, FDA regulations, and CE marking can set you apart from other candidates.
✨Tip Number 3
Consider reaching out to current or former employees of the company. They can provide valuable information about the company culture and expectations for the Quality Assurance & Regulatory Affairs Officer role.
✨Tip Number 4
Prepare for potential interviews by practising common questions related to quality assurance and regulatory compliance. Be ready to discuss specific examples from your past experience that demonstrate your expertise in these areas.
We think you need these skills to ace Quality Assurance & Regulatory Affairs Officer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your quality assurance and regulatory experience, especially within the medical devices sector. Use specific examples to demonstrate your skills and achievements relevant to the role.
Craft a Compelling Cover Letter: Write a cover letter that clearly outlines your motivation for applying and how your background aligns with the job requirements. Mention your experience in managing quality systems and conducting audits, as these are key aspects of the role.
Highlight Relevant Skills: In your application, emphasise your understanding of quality and regulatory requirements. Include any certifications or training you have completed that are pertinent to the medical sector.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in quality assurance roles.
How to prepare for a job interview at TN United Kingdom
✨Know Your Regulations
Familiarise yourself with the key regulations and standards relevant to the medical devices sector, such as ISO 13485 and FDA guidelines. Being able to discuss these in detail will demonstrate your expertise and commitment to quality assurance.
✨Prepare for Technical Questions
Expect technical questions related to quality systems and regulatory compliance. Brush up on your knowledge of quality assurance processes, audit procedures, and how to resolve quality issues effectively.
✨Showcase Your Experience
Be ready to share specific examples from your previous roles that highlight your experience in quality assurance and regulatory affairs. Use the STAR method (Situation, Task, Action, Result) to structure your responses.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's quality systems and regulatory challenges. This shows your genuine interest in the role and helps you assess if the company aligns with your career goals.
