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- Tasks: Lead regulatory compliance and Post Market Surveillance for medical devices.
- Company: Join a fast-growing global medical device organisation with a supportive culture.
- Benefits: Hybrid work, high-impact role, and opportunities for professional growth.
- Why this job: Make a real difference in patient safety and product innovation.
- Qualifications: Degree in Science, Medical, or Engineering and 3+ years in Regulatory Affairs.
- Other info: Collaborative team environment with ownership and visibility in your role.
The predicted salary is between 40000 - 50000 £ per year.
Join a growing global medical devices business and take ownership of regulatory compliance across key markets. We’re looking for an experienced Regulatory Affairs professional to lead Post Market Surveillance (PMS) activities and support global regulatory submissions across EU, UK, US, and international markets.
Key Responsibilities:
- Lead Post Market Surveillance (PMS): PMS Plans, PSUR, PMCF documentation
- Prepare and maintain Technical Files / Technical Documentation (EU MDR)
- Support Regulatory Submissions: MHRA, FDA, GUDID, FURLS
- Ensure compliance with EU MDR, UK MDR, FDA, ISO 13485, ISO 14971
- Partner cross-functionally on New Product Development (NPD)
- Support QMS, audits, vigilance, and complaints handling
- Review labelling, packaging, and IFUs for regulatory compliance
Requirements:
- Degree in Science, Medical, or Engineering discipline
- 3 years or more Regulatory Affairs experience (Medical Devices)
- Strong experience in Post Market Surveillance & Clinical Evaluation
- Proven ability with Technical Documentation / Dossiers
- Knowledge of global regulatory frameworks (EU, UK, US)
- Highly organised, detail-driven, and confident managing multiple priorities
Why GBUK?
- Global, fast-growing medical device organisation
- High-impact role with ownership and visibility
- Collaborative, supportive team culture
- Opportunity to influence patient safety and product innovation
Apply now or get in touch to find out more.
Senior Regulatory and Post Market Affairs Associate in Glasgow employer: GBUK
Contact Detail:
GBUK Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Regulatory and Post Market Affairs Associate in Glasgow
✨Tip Number 1
Network like a pro! Reach out to professionals in the regulatory affairs field on LinkedIn or at industry events. A friendly chat can open doors and give you insights that job descriptions just can't.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of EU MDR, UK MDR, and FDA regulations. We want you to be the go-to person for compliance questions, so show off your expertise!
✨Tip Number 3
Practice your STAR technique for answering behavioural interview questions. We love hearing about your past experiences, so structure your answers to highlight your achievements in Post Market Surveillance and Technical Documentation.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows us you’re genuinely interested in joining our team at GBUK.
We think you need these skills to ace Senior Regulatory and Post Market Affairs Associate in Glasgow
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Regulatory and Post Market Affairs Associate role. Highlight your experience in regulatory compliance, especially with EU MDR and FDA submissions, as well as your skills in Post Market Surveillance.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for this role. Mention specific experiences that align with the key responsibilities, like leading PMS activities or preparing technical documentation.
Showcase Your Organisational Skills: Since this role requires managing multiple priorities, make sure to highlight your organisational skills. Share examples of how you've successfully juggled tasks in previous roles, particularly in a regulatory affairs context.
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates!
How to prepare for a job interview at GBUK
✨Know Your Regulations
Make sure you brush up on the key regulations like EU MDR, UK MDR, and FDA guidelines. Being able to discuss these confidently will show that you’re not just familiar with the requirements but also passionate about compliance.
✨Showcase Your Experience
Prepare specific examples from your past roles where you successfully led Post Market Surveillance activities or managed regulatory submissions. This will help demonstrate your hands-on experience and problem-solving skills in real-world scenarios.
✨Be Detail-Driven
Since this role requires a high level of organisation and attention to detail, be ready to discuss how you manage multiple priorities. Share tools or methods you use to stay organised, especially when preparing Technical Documentation or handling audits.
✨Engage with Cross-Functional Teams
Highlight your experience working with cross-functional teams, especially in New Product Development. Discuss how collaboration has led to successful outcomes in your previous roles, as this will resonate well with their team culture.