At a Glance
- Tasks: Transform clinical evidence into impactful documentation for innovative medical devices.
- Company: Smith+ is a forward-thinking tech company dedicated to improving lives.
- Benefits: Generous bonuses, flexible vacation, health plans, and employee discounts.
- Other info: Enjoy a hybrid working model and excellent career development opportunities.
- Why this job: Join a mission-driven team shaping the future of healthcare with your expertise.
- Qualifications: Experience in medical writing and understanding of clinical evaluation processes.
The predicted salary is between 63000 - 77000 £ per year.
Life. Unlimited. At Smith+… we design and manufacture technology that takes the limits off living. Are you passionate about turning clinical evidence into meaningful impact? This is an opportunity to play a critical role in ensuring innovative medical devices continue to meet the highest standards of safety, performance and regulatory compliance.
In this role, you will bring together scientific expertise, medical writing and regulatory understanding to create robust clinical evidence documentation that underpins the continued CE registration of Smith+… products. You will immerse yourself in clinical data, literature and post market insights, translating complex information into clear, high quality documentation that demonstrates product safety and performance.
Working closely with cross functional partners, you will act as a trusted subject matter expert, supporting audits, submissions and strategic business decisions that determine whether products can be placed on the market and how they evolve over time.
What will you need to be successful?
- Strong experience in medical or scientific writing, with the ability to critically appraise and synthesise clinical evidence in line with EU MDR and other related guidance.
- A solid understanding of clinical evaluation processes, literature review methodologies and benefit risk assessment within medical devices or a closely related regulated environment.
- The confidence to act as a subject matter expert, engaging with cross functional teams and supporting regulatory interactions, audits and submissions.
- A proactive and organised approach, with the ability to manage complex documentation, deadlines and priorities independently while working as part of a collaborative team.
You. Unlimited. We believe in creating the greatest good for society. Our strongest investments are in our people and patients we serve.
Inclusion and Belonging: Committed to Welcoming, Celebrating and Thriving on Inclusion and Belonging.
Your Future: Generous annual bonus and pension schemes, Save As You Earn share options.
Work/Life Balance: Flexible vacation and time off, paid holidays and paid volunteering hours, so we can give back to our communities!
Your Wellbeing: Private health and dental plans, healthcare cash plans, income protection, life assurance and much more.
Flexibility: Hybrid working model (for most professional roles).
Training: Hands-on, team-customised, mentorship.
Extra Perks: Discounts on gyms and fitness clubs, salary sacrifice bicycle and car schemes and many other employee discounts.
Senior Specialist, Evidence Evaluation United Kingdom employer: Meeveem Limited
Meeveem Limited is an exceptional employer that values its employees by fostering a collaborative and innovative work culture in the heart of Yorkshire. With a strong focus on professional development, employees are encouraged to grow their skills and advance their careers while enjoying competitive benefits and a supportive environment that prioritises work-life balance. Joining Meeveem means being part of a dynamic team dedicated to making a meaningful impact in the cardiovascular and endovascular sectors.
