RA/QA Specialist-Career Growth Opportunity-Medical Devices
Are you looking for an opportunity within regulatory affairs and quality assurance that will give you career growth prospects on an international scale, across class I through to class III medical devices. You will gain invaluable expertise from this regulatory affairs and quality assurance role that will not only lead to an enriching working life but will enhance your career prospects in the future. Apply now to find out more.
As the regulatory and quality specialist in this role your responsibilities will include but will not be limited to:
- You will be working on the full product life cycle, allowing you to be part of all the processes and develop your expertise from start to finish.
- Develop the QMS and audit system with the director of regulatory affairs and quality.
- Work on an international sclae, where you will develop key expertise in some of the most exciting and growing emerging markets.
The ideal candidate for this role will come from a quality and regulatory background within the medical device industry. You will have good working knowledge of ISO 13485 and have worked on an international scale. You are fluent in both English and German.
Take the first step today towards enriching your career within regulatory affairs and quality assurance today! Take your career to international heights.
Call me Tamanna Gandecha at NonStop Recruitment now for a confidential conversation. Contact me on firstname.lastname@example.org 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 associate, regulatory affairs specialist, regulatory affairs, quality assurance, quality assurance specialist, medical devices, registration, nonstop recruitment, medical device jobs, switzerland