Regulatory Affairs Team Lead-Global Medical Devices-Hamburg

Regulatory Affairs Team Lead-Global Medical Devices-Hamburg, Germany

NonStop Medical Devices are currently recruiting for an excellent opportunity to train and develop an international team within the regulatory affairs department. If you are looking for a senior team lead and strategic role, then ensure you apply today to find out more.

As the head of regulatory affairs in this role your responsibilities will include but will not be limited to:

• Preparing strategy for new product development.
• Managing the project teams for international submission inclusive of Europe, China and the US. The team will be around six strong to start with.
• Working across different departments to ensure successful regulatory submission, inclusive of R&D and marketing.
• Key representative for the company at global events.
• Responsible for the successful regulatory and quality registration process.

The ideal candidate for this role will have:

• A strong background within regulatory affairs for the medical device industry.
• Currently has or has led teams, thus can exemplify key leadership skills.
• Understanding the administrative and disciplinary aspect of managing a team.
• Working knowledge of ISO 13485.
• Fluency in both English and German.

Ensure you apply now to find out more about this new and exciting leadership role within regulatory affairs.

Call me Tamanna Gandecha at NonStop Recruitment now for a confidential conversation. Contact me on regulatory@nonstop-devices.com or +41 435 0808 16, please send your CV in word format OR if this does not sound like the opportunity for you, but you are a regulatory affairs professional within the medical device industry, please feel free to get in touch, to see other opportunities we may have within this field.

NonStop is one of the largest and fastest growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences across Europe. Please visit our website for a full list of the niche markets we cover.

What I offer: As a specialist Headhunter within regulatory affairs for the medical device industry I can offer: market knowledge and a personal service, therefore not just finding you suitable roles but in addition to this offering accurate and honest advice about salaries, work conditions and department reputations for positions across Switzerland.

KEY WORDS: regulatory affairs, regulatory affairs manager, head of regulatory affairs, quality assurance, IVD, diagnostics, switzerland, zurich, nonstop recruitment, ISO 13485, nonstop medical devices