Project Manager-Full Product Life Cycle-Devices-Zurich, CH

Location
Zürich
Salary
£78530 - £86383 per annum
Posted
Jul 31, 2017
Closes
Aug 30, 2017
Ref
TG/58625/1
Contact
Tamanna Gandecha
Jobseeker Type
Professional
Organization Type
Corporate
Contract Type
Employee
Hours
Full Time

Project Manager-Full Product Life Cycle-Devices-Zurich, Switzerland

An exciting role to work across the full product life cycle of a world leading medical device company has come in within the Zurich region in Switzerland. This is a great opportunity to work with innovative medical devices, working from research and development through to quality and regulatory affairs. Through this full life cycle role you will gain a varied role where you will gain invaluable expertise across a great deal of cross-function work. Apply today to find out more.

As the project manager in this role your responsibilities will include but will not be limited to:

  • Working across multiple departments coordinating the QA, RA and research and development department. With a primary focus on research and development.
  • Provide key support to stakeholders.
  • Drive forward innovation and development within the business.
  • Coordinate and advise the senior management on progression planning for the future.

The ideal candidate for this role will have worked for several years within the medical device industry, in a project management role; where you have focused your career within research and development. You will have good working knowledge of ISO 13485. You will have worked closely in the cross-function teams in the specific areas of regulatory affairs and quality assurance. You will speak fluent English, where fluency in German would be a bonus.

Apply now to find out more about this excellent project manager role and develop your career in a key strategic role.

Call me Tamanna Gandecha at NonStop Recruitment now for a confidential conversation. Contact me on t.gandecha@nonstop-recruitment.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.

KEY WORDS: research and development, project manager, project management, medical devices, regulatory affairs, quality assurance, ISO 13485, switzerland, nonstop recruitment, medical device jobs