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Senior Regulatory Affairs Specialist

Senior Regulatory Affairs Specialist

  • Location

    Basel, Switzerland

  • Sector:

    Regulatory Affairs

  • Job type:

    Permanent

  • Salary:

    140000

  • Contact:

    Cheikh Khoule

  • Contact email:

    cheikh.khoule@catalystcareers.com

  • Job ref:

    53235

  • Published:

    10 months ago

  • Expiry date:

    2020-09-07

  • Consultant:

    #

Vacancy Details

 

My client, a Global Medical devices company are looking for a Senior Regulatory Affairs Specialist based in Basel.

 

A great opportunity to join a fast-growing company with a great portfolio of products.

 

Senior Regulatory Affairs Specialist

Location: Basel

Salary: Up to 140,000 CHF

Duration: Permanent

 

Job function:

  • Supporting of international registration submissions
  • Ensuring that regulatory requirements for the approval of medical devices are met during the product development process

· Supporting in the preparation and execution of audits

  • Communicating of new regulatory approval requirements

· Participating in the respective product development teams

 

To be considered you need to have

  • Eligibility to work in Switzerland
  • 3+ years’ experience in global regulatory affairs experience
  • MDD experience - Mandatory
  • English fluent - Mandatory
  • MDR experience - Desirable
  • German fluent - Desirable

 

I will also look for an RA manager and QA/RA manager in different Germany

 

Looking but this isn’t the right position for you?

If you are interested in a new opportunity but your experience doesn't fit this role, please email your CV and the best time for a call to cheikh.khoule@catalystcareers.com to setup a confidential discussion about potential opportunities.

 

NOT OF INTEREST TO YOU BUT KNOW SOMEONE IT WOULD BE?

CLS offer a generous referral scheme reward, whereby anyone who refers us to a successfully placed candidate is entitled to up to £250 worth of vouchers.

 

Catalyst Life Sciences

CLS are a global recruitment company operating in the Life Sciences space, with specialist consultants working within the technical and regulatory areas. This includes the following markets.

  • Pre-clinical Development & Safety
  • Clinical Development
  • Medical Affairs & Information
  • Regulatory Affairs
  • Pharmacovigilance/Drug Safety
  • Quality & Validation
  • Finance

 

My Linked In Profile

 

linkedin.com/in/cheikh-khoule

 

I personally specialise in recruiting QA, RA and validation professionals for roles across DACH so please do get in touch should you be considering new roles or looking to fill ones at your current company!

 

KEYWORDS

 

RA / regulatory / MDD / MDR / devices / 13485 / submission / regulatory / FDA / CFR / 21