Medical device safety manager
Medical device safety manager

Medical device safety manager

Full-Time 36000 - 60000 Β£ / year (est.) No home office possible
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At a Glance

  • Tasks: Join a team ensuring the safety of medical devices and lead compliance initiatives.
  • Company: Be part of a global life sciences organisation making a difference in healthcare.
  • Benefits: Enjoy hybrid working options and opportunities for professional development.
  • Why this job: Make an impact in patient safety while collaborating with industry experts.
  • Qualifications: A degree in life sciences and experience in medical device safety are essential.
  • Other info: This is a 12-month contract role based in the UK.

The predicted salary is between 36000 - 60000 Β£ per year.

Job Description

Job Title: Medical Devices Clinical Safety Team Member

Contract Duration: 12 months (15/09/2025 – 14/09/2026)

Start Date: 15/09/2025

Location: Office-based, hybrid considered

Right to Work: Full UK RTW required (no sponsorship)

Overview:

We are seeking a highly experienced Medical Devices Clinical Safety professional to join a global life sciences organization. The ideal candidate will bring deep expertise in medical device (MD) and/or in-vitro diagnostic (IVD) safety within the pharmaceutical, biotech, or medical device industry.

Key Responsibilities:

  • Contribute as a core member of the Medical Devices Clinical Safety Team
  • Act as subject matter expert on MD/IVD safety and regulatory compliance
  • Lead or support development and implementation of MD safety processes
  • Provide consultation to safety teams and internal stakeholders
  • Participate in safety reviews, audits, CAPAs, and expert group forums
  • Contribute to training and mentoring of colleagues in MD safety
  • Stay current on industry standards, trends, and regulatory changes

Requirements:

  • University degree (preferably in life sciences) or equivalent professional experience
  • Extensive experience in MD or IVD safety
  • Familiarity with global MD safety regulations and standards
  • Strong knowledge of pharmacovigilance and clinical safety integration
  • Proven ability to work cross-functionally and influence stakeholders
  • Excellent communication, leadership, and collaboration skills

Preferred:

  • Experience with combination products or due diligence evaluations
  • Involvement in expert safety groups or training initiatives

Medical device safety, clinical safety, in-vitro diagnostics, IVD, pharmacovigilance, combination products, medical device regulations, risk management, CAPA, audit support, clinical safety specialist, medical device clinical safety lead, process improvement, safety signal detection, regulatory compliance, cross-functional collaboration, safety governance, SOP development, WI development, global safety standards, due diligence, safety team member, medical device expert, ISO 13485, FDA 21 CFR Part 820, GxP compliance, device vigilance, safety training, stakeholder engagement, technical documentation, lifecycle safety management, clinical investigations, safety risk assessment, hybrid working, life sciences, biotech, safety strategy, audit readiness, safety data analysis, global safety processes

Medical device safety manager employer: Unity Systems

Join a leading global life sciences organisation that prioritises employee growth and development, offering a collaborative work culture where your expertise in medical device safety will be valued. With opportunities for hybrid working and a commitment to staying at the forefront of industry standards, this role not only promises meaningful contributions to patient safety but also fosters a supportive environment for professional advancement.
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Contact Detail:

Unity Systems Recruiting Team

StudySmarter Expert Advice 🀫

We think this is how you could land Medical device safety manager

✨Tip Number 1

Network with professionals in the medical device safety field. Attend industry conferences, webinars, or local meetups to connect with others who work in this area. Building relationships can lead to valuable insights and potential job referrals.

✨Tip Number 2

Stay updated on the latest regulations and standards related to medical devices and in-vitro diagnostics. Subscribe to relevant journals or follow industry leaders on social media to ensure you’re aware of any changes that could impact your role.

✨Tip Number 3

Consider joining professional organisations or groups focused on medical device safety. These platforms often provide resources, training opportunities, and forums for discussion that can enhance your knowledge and visibility in the field.

✨Tip Number 4

Prepare for interviews by practising common questions related to medical device safety and regulatory compliance. Be ready to discuss specific examples from your experience that demonstrate your expertise and problem-solving skills in this area.

We think you need these skills to ace Medical device safety manager

Medical Device Safety Expertise
In-Vitro Diagnostic Safety Knowledge
Regulatory Compliance Understanding
Pharmacovigilance Skills
Clinical Safety Integration
Cross-Functional Collaboration
Stakeholder Engagement
Risk Management
CAPA (Corrective and Preventive Actions) Management
Audit Support
Safety Signal Detection
SOP Development
Technical Documentation Skills
Lifecycle Safety Management
Safety Data Analysis
ISO 13485 Familiarity
FDA 21 CFR Part 820 Knowledge
GxP Compliance Awareness
Training and Mentoring Abilities
Process Improvement

Some tips for your application 🫑

Tailor Your CV: Make sure your CV highlights your experience in medical device safety and regulatory compliance. Use specific examples that demonstrate your expertise in MD/IVD safety, pharmacovigilance, and cross-functional collaboration.

Craft a Compelling Cover Letter: In your cover letter, express your passion for medical device safety and how your background aligns with the role. Mention any relevant projects or achievements that showcase your ability to lead safety processes and mentor colleagues.

Highlight Relevant Skills: Clearly outline your skills related to safety governance, risk management, and regulatory compliance. Emphasise your familiarity with global MD safety regulations and standards, as well as your experience with audits and CAPAs.

Showcase Continuous Learning: Mention any recent training, certifications, or industry conferences you’ve attended that relate to medical device safety. This demonstrates your commitment to staying current on industry standards and trends.

How to prepare for a job interview at Unity Systems

✨Know Your Regulations

Familiarise yourself with global medical device safety regulations and standards. Being able to discuss these in detail will demonstrate your expertise and show that you are up-to-date with industry requirements.

✨Showcase Your Experience

Prepare specific examples from your past roles where you contributed to MD/IVD safety processes or led safety reviews. This will help illustrate your hands-on experience and problem-solving skills.

✨Emphasise Cross-Functional Collaboration

Highlight instances where you've successfully worked with different teams or stakeholders. This role requires strong collaboration, so showcasing your ability to influence and engage others will be key.

✨Stay Current on Trends

Research recent trends and changes in the medical device industry. Being able to discuss these topics during your interview will show your passion for the field and your commitment to continuous learning.

Medical device safety manager
Unity Systems
U
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