At a Glance
- Tasks: Lead regulatory strategies for innovative FemTech products and ensure compliance across global markets.
- Company: Join Elvie, a pioneering FemTech company transforming maternal health with cutting-edge technology.
- Benefits: Enjoy a flexible 9-day fortnight, generous leave policies, and comprehensive healthcare plans.
- Other info: Work remotely in a diverse, inclusive environment that values your unique contributions.
- Why this job: Be part of a mission-driven team empowering women through radical innovation in health technology.
- Qualifications: Experience in medical device regulatory affairs and a relevant degree are essential.
The predicted salary is between 60000 - 75000 £ per year.
We’re Elvie – a pioneer in the FemTech industry, developing cutting-edge smart technology to transform previously overlooked categories like breast pumping and pelvic floor health. Our mission is to empower women through radical, female-first innovation, breaking taboos and challenging stigma along the way.
Elvie recently joined forces with Willow, a fellow leader in FemTech and maternal health based in the U.S. This powerful combination brings together two iconic brands, combining a market-leading product portfolio with teams of world-class engineers, designers, and commercial experts. Together, we're set to shape the future of maternal health on a global scale.
As we embark on this exciting new transitional chapter, this role will play a pivotal part in helping to define and deliver our vision across international markets.
Did you know? In some regions our amazing products are considered to be medical devices. This means we maintain our Medical Device quality management system in compliance with ISO 13485:2016, to support the development of our groundbreaking products.
About the role:
Elvie has a need for a detail-oriented, passionate and dynamic individual with a desire to be an integral part of our growing Quality and Regulatory team. You respect rules and regulations but are not afraid to do things differently and challenge ‘business as usual’. You are able to understand and interpret global regulations to support the strategic placement of our growing portfolio of both medical and non-medical products into world-wide markets. Provide guidance to the cross-functional teams to successfully support and drive products to market, from R&D and Product Development, through to Sales and Marketing.
You are organised and logical and can form a clear path through the noise when complex decisions need to be made. You are able to work autonomously and be the authoritative voice for Regulatory Affairs. You can develop plans of action and communicate them with confidence to all functions and levels within the business.
You will have experience working within the Medical Device industry, in a global regulatory focused role. You are excited by the prospect of defining the regulatory strategy and best practices in a rapidly growing and exciting business. Experience with multi category product portfolios (consumer electronics, childcare products, cosmetics, etc) is highly desirable.
Location: UK, Remote Employment type: Permanent (please note, you must have the right to work in the UK)
What you’ll be doing at Elvie:
- Partner with cross functional teams to develop global regulatory requirements and timelines that align with the business expansion and new product launches.
- Provide clear and unambiguous guidance on regulatory requirements for new market entry and design changes for medical devices, childcare products and consumer goods.
- Lead regulatory submissions to support new product launches including the development and maintenance of FDA 510(k)’s, Technical Files and Essential Requirements Checklists.
- Communicate with world-wide agencies, in-country representatives and regulatory bodies to support our products.
- Understand new or changing regulatory landscapes that could impact our products.
- Support the development and continual improvement of internal regulatory processes.
What we are looking for:
- A degree in a relevant engineering, design or science discipline (or equivalent qualification).
- Extensive experience in medical device regulatory affairs including direct experience working with EU Notified Bodies, EU Authorised Representatives, MHRA, US FDA, FCC and Health Canada. Experience in product placement in MDSAP countries would be an advantage.
- Ability to interpret worldwide regulations to ensure uninterrupted supply of our products to our customers.
- Experience ensuring a high level of compliance with MDR, ISO 13485, 21 CFR 820.
- Must be familiar with commonly used productivity & statistical software such as Microsoft Office, Google suite and eQMS solutions.
The benefits you’ll get:
We're on an exceptional journey. And we can offer you a genuinely purpose-led career with a culture built on trust, autonomy, and flexibility. In addition, we'll give you:
- 9-day fortnight working pattern - for our full time employees we work 9 days every fortnight with every other Friday as a non-working day for you to spend as you wish.
- Lots of flexibility: whether it’s working from home, doing the school run, or life admin. We believe trust and flexibility allows everyone to show up as their best selves.
- 25 days’ annual leave, plus bank holidays.
- Life leave days; getting married, moving house, menopause or just things that you can’t put a label on that matter to you.
- 5=10 leave: 10 days’ additional leave on your 5th and 10th years of service.
- Generous parental leave policies; maternity & adoption (16 weeks at full pay, then 8 weeks paid at 75% followed by 15 weeks at SMP rate), paternity/partner (6 weeks at full pay to take at any point during the first year of your child’s life), shared parental leave.
- Healthcare plans, life insurance, and an employee assistance program for you and your family.
- A tax-efficient group pension scheme.
- Group income protection; protect your salary if you get sick.
- Generous employee and friends & family discounts on Elvie products.
- Wellbeing support from YuLife and access to SmartHealth app with unlimited GP appointments for you and your family.
What you can expect after you’ve applied:
A member of our team will reach out to you after they have reviewed your application. You must ensure your application is completed correctly. We do often receive a large number of applications for our roles, please don’t let visibility of this deter you from applying. We review and aim to respond to every application.
We would like to get to know you through your background, attitude, experience and understand your motivation to work with us. Our interview process varies depending on the position.
This is an exciting time to join Elvie. You’ll have a voice, make an impact, and have the opportunity to mould your role. So be ready to learn, have fun, and be inspired by our passionate, talented team - having a sense of humour helps too.
Belonging at Elvie
At Elvie, we value building broad, diverse and inclusive teams - because we believe everyone being able to show up authentically at work is key to our success. We encourage people from all backgrounds to apply and we don't discriminate based on race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, marital status, disability or age.
If you would like more information about the role (including salary) or need any support with your application please feel free to get in touch by email recruitment@elvie.com.
Manager/Sr. Manager- Regulatory & Clinical Affairs employer: Elvie
Elvie is an exceptional employer that champions a purpose-led culture, offering a unique 9-day fortnight working pattern and extensive flexibility to support work-life balance. With a strong commitment to employee growth, generous parental leave policies, and comprehensive wellbeing support, Elvie empowers its team to thrive in a dynamic FemTech environment, making a meaningful impact on women's health globally.
StudySmarter Expert Advice🤫
We think this is how you could land Manager/Sr. Manager- Regulatory & Clinical Affairs
✨Tip Number 1
Network like a pro! Reach out to people in the FemTech industry, especially those who work at Elvie or similar companies. A friendly chat can open doors and give you insider info that could help you stand out.
✨Tip Number 2
Prepare for your interview by knowing Elvie's products inside out. Show us you’re passionate about our mission and how you can contribute to our regulatory and clinical affairs. Bring your A-game!
✨Tip Number 3
Practice your answers to common interview questions, but keep it natural. We want to see your personality shine through, so don’t be afraid to let your enthusiasm for the role show!
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re serious about joining our amazing team at Elvie.
We think you need these skills to ace Manager/Sr. Manager- Regulatory & Clinical Affairs
Some tips for your application 🫡
Show Your Passion:When writing your application, let your enthusiasm for the FemTech industry shine through. We want to see that you’re not just qualified, but genuinely excited about empowering women and breaking taboos with innovative technology.
Tailor Your CV:Make sure your CV is tailored to highlight your experience in regulatory affairs, especially within the medical device sector. We love seeing how your background aligns with our mission and the specific requirements of the role.
Be Clear and Concise:In your cover letter, get straight to the point. We appreciate clarity, so outline your relevant experience and how it relates to the role without waffling. Remember, we’re looking for someone who can communicate effectively across teams!
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity. Plus, it shows you’re keen to join our team at Elvie!
How to prepare for a job interview at Elvie
✨Know Your Regulations
Familiarise yourself with the specific regulations relevant to the medical device industry, especially those pertaining to ISO 13485 and FDA guidelines. Being able to discuss these in detail will show your expertise and readiness for the role.
✨Showcase Your Experience
Prepare to share specific examples from your past roles that demonstrate your experience with regulatory submissions and compliance. Highlight any successful product launches you've been involved in, particularly in the FemTech or medical device sectors.
✨Understand Elvie's Mission
Research Elvie’s products and their impact on women's health. Be ready to discuss how your values align with their mission of empowering women through innovation. This will help you connect on a personal level during the interview.
✨Prepare Questions
Think of insightful questions to ask about the company culture, team dynamics, and future projects. This shows your genuine interest in the role and helps you assess if Elvie is the right fit for you.