project manager (mdr) in zuchwil

job type
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job details

zuchwil, solothurn
job category
Life Sciences
job type
reference number
058 201 55 50

job description

Randstad Professionals is currently looking for a Project leader/ project manager who will be assigned an interesting challenge for a major client based in the canton of Solothurn . This contract is an unique opportunity to join a major global group focusing on the Healthcare/ vaccines Manufacturing sector. The initial assignment will start in December 2019 and will last until August 2020. Our client is a major name in the Pharmaceutical arena. 


Assignment details:

Start Date:   December 2019

Requisition End Date:   31/07/2020




1. Overall responsibilities 

the project manager s responsible for the project management role for the update of the technical documentation of existing electromechanical medical devices according to MDR.


2. Position duties and responsibilities 

  • Project controlling of the Power Tool MDR Project 

  • Performs the required project management activities for the MDR project (e.g. report project status to management, coordinate project activities, update project timeline, organize meetings, support Lead Sustaining Engineering to define work packages and project plan) 

  • Works together with regulatory, quality, technical engineering, external suppliers and manufacturing to achieve the project goals 

  • Knowledge and compliance with laws and policies that apply to the job and ensure a high level of professionalism, ethics and compliance at all time 


3. Your Profile


  • Master/ bachelor’s degree in mechanical/ mechatronics/ electrical/ design quality engineering or management 

  • At least 3 years of experience in project management of cross functional projects 

  • At least 2 years of experience in the medical device industry or regulated industry 

  • Business fluent English and good German (minimum B2 level) 

  • MS Office (Work, Excel, Outlook) knowledge is required. 

  • Communication skills 

  • Creative/problem-solving skills 


• Minimum 2 years as Project manager in a regulated environment 

• Experience with Medical device Regulation will top your profile   (EMA / MDR) 


If you are interested to learn more about this great opportunity, don’t hesitate to get in touch with me. Feel free to send me your CV at following email

I am looking forward to receiving your applications


Olivier Worch


Randstad Professionals Basel