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- Tasks: Ensure quality and compliance in medical devices through audits and documentation.
- Company: Leading medical device company based in Liverpool with a strong reputation.
- Benefits: Full-time role with competitive salary and opportunities for professional growth.
- Why this job: Join a vital industry and make a difference in healthcare quality and safety.
- Qualifications: Bachelor's degree and 2-3 years' experience in Quality Assurance or Regulatory Affairs.
- Other info: Dynamic work environment with a focus on innovation and compliance.
The predicted salary is between 36000 - 60000 £ per year.
A leading company in medical devices based in Liverpool is seeking a proactive Quality & Regulatory Affairs Officer. The successful candidate will maintain QMS documentation, conduct internal audits, and ensure compliance with UK and international regulations.
Ideal applicants will have a Bachelor's degree and 2-3 years' experience in Quality Assurance or Regulatory Affairs within the medical devices sector. Exceptional communication and technical writing skills are required for this full-time role.
QA & Regulatory Affairs Specialist – Medical Devices employer: SRG
Contact Detail:
SRG Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QA & Regulatory Affairs Specialist – Medical Devices
✨Tip Number 1
Network like a pro! Reach out to professionals in the medical devices sector on LinkedIn. Join relevant groups and engage in discussions to get your name out there and learn about potential job openings.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of QMS documentation and regulatory compliance. We recommend practising common interview questions related to Quality Assurance and having examples ready to showcase your experience.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, send a thank-you email to express your appreciation and reiterate your interest in the role. It shows professionalism and keeps you on their radar.
✨Tip Number 4
Apply through our website for the best chance at landing that QA & Regulatory Affairs Specialist role. We make it easy for you to showcase your skills and experience directly to employers looking for talent like yours!
We think you need these skills to ace QA & Regulatory Affairs Specialist – Medical Devices
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in Quality Assurance and Regulatory Affairs, especially within the medical devices sector. We want to see how your skills match up with what we're looking for!
Show Off Your Communication Skills: Since exceptional communication is key for this role, include examples of how you've effectively communicated complex information in your previous jobs. We love seeing those technical writing skills in action!
Be Proactive in Your Cover Letter: Use your cover letter to demonstrate your proactive approach. Share specific instances where you took initiative in maintaining QMS documentation or conducting audits. We appreciate candidates who take charge!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy!
How to prepare for a job interview at SRG
✨Know Your Regulations
Familiarise yourself with UK and international regulations related to medical devices. Be prepared to discuss how these regulations impact Quality Management Systems (QMS) and your previous experiences in ensuring compliance.
✨Showcase Your Auditing Skills
Since conducting internal audits is a key part of the role, think of specific examples where you've successfully performed audits. Highlight any improvements you made as a result, demonstrating your proactive approach.
✨Communicate Clearly
Exceptional communication skills are a must. Practice articulating complex regulatory concepts in simple terms. This will show that you can effectively communicate with both technical and non-technical stakeholders.
✨Prepare Your Technical Writing Samples
Bring along samples of your technical writing, such as QMS documentation or reports. Be ready to discuss your writing process and how you ensure clarity and compliance in your documents.
