Elemed is Europe’s leading MedTech technical recruiter. We serve within the Medical device, diagnostic and combination device arena, working with Managers up to VP of Quality and Regulatory. Our team helps medical device experts of today become leaders of tomorrow.
At Elemed, we recruit exceptional people that solve regulatory and compliance problems, so patients can have access to safe, innovative and life-changing Medical Devices.
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status
Head of Regulatory Affairs
Job Title: Head of Regulatory Affairs
Location: Zurich, Switzerland or home based (up to 1hr from Zurich.)
A growing Swiss medical device consultancy is developing a new Regulatory Affairs business unit and is offering a unique opportunity for an experienced Regulatory professional to use their skills in a new way. This is a permanent position, offering stability, the opportunity to build something, and a role blending all the classic regulatory skills in a new context.
As Head of Regulatory Affairs your mission will be to set and implement the growth strategy for your own regulatory affairs business unit. The role’s responsibilities covers 3 core areas:
Define the business unit’s annual goals in line with the company’s overall vision
Develop the hiring strategy for your new team along with associated milestones and timelines
Hire, train and lead a team of regulatory consultants and empower them to reach their goals
Report on and represent your business unit in leadership meetings and discussions with the CEO on KPIs, pipeline and overall business unit performance.
Build and manage a pipeline of projects by proactively networking within the industry, in person and virtually, delivering webinars and attending relevant industry events
Develop & implement strategies for new customer acquisition
Identify potential opportunities for the introduction of new solutions to support the client’s need
Supporting “hands on” regulatory projects for customers on activities spanning the full lifecycle of a medical device: CE marking, New product introductions, regulatory strategy, PMS, and more
Supporting with MDR/IVDR strategy and implementation
Providing solutions and ad hoc consulting subject to the client’s needs
Why does Elemed love this opportunity?
This is a chance to build something and make your mark!
No two days will be the same! This role offers alot of variety and creativity.
You’ll be part of board meetings and have your voice and ideas heard by the CEO
You will play a lead role in all projects related to regulatory affairs and have direct customer interaction.
This role also offers a great salary and benefit package where you will benefit from a profit share of the business unit!
As the Head of Regulatory Affairs you should have:
7+ years experience in regulatory affairs, medical devices or diagnostics
Commercial mindset & problem solving approach
Fluent German & English
Be part of the future legacy of a growing business! If you are interested in this position, please contact Elena at firstname.lastname@example.org for a confidential career discussion.
ELEMED EUROPE Ms Elena Kyriacou Heinrichstrasse 267 ? 267a 8005 Zürich +41215391933