Connecting

Regulatory Affairs Specialist/Manager (m/w) - global Medical Device company - Zug

Job title: Regulatory Affairs Specialist/Manager (m/w) - global Medical Device company - Zug
Contract Type: Permanent
Location: Switzerland, Liquid error: internal
Industry:
Salary: Competitive
Reference: BH-124676
Contact Name: Martin Ivanov
Phone Number: +41 (0)43 588 16 16
Job Published: 23 days ago

Job Description

Regulatory Affairs Specialist/Manager (m/w) - global Medical Device company - Zug

NES Global Talent in Switzerland focuses purely in the Life Science sector where we support the Pharma, Medical Device, Biotech industries and work on QA, Technical and Regulatory positions. With a database that consists of over 2000 Life Science involved talents based in Switzerland and a contact that covers 90% of the job seekers we advertise our clients through all recruitment rotes on a daily basis.

Currently we support one of our clients in the Medical Device industry and in order to strengthen their team, we are looking for an experienced professional to join them as a Regulatory Affairs Specialist/Manager. Their current and upcoming projects in Q4 2020 and Q1 2021 predict growth in the Regulatory department and they've reached to us for our support.

Responsibilities:
  • Regulatory Tender documentation
  • Environmental regulatory compliance experience (not mandatory, good to have)
  • Train sales & marketing employees on Regulatory Affairs (concept, idea, meaning, importance)
  • Support product/process development and the requirements in the relevant local market & industry

Required skills:
  • Regulatory commercial operations support experience
  • Product registration in EMEA
  • CE-Marking experience
  • Fluent English, good to have German or French

What to expect:
  • Detailed conversation, introduction and preparation for a successful application with an experienced consultant
  • Transparency and support throughout the application process
  • Negotiation with clients for better work/contract conditions
  • Follow up and update on market relevant opportunities
 
Experience in within the EU is needed. Please note we can only accept applications from candidates who hold valid European Union passport and are able to work in Europe without visa sponsorship.

For a confidential discussion about quality assurance vacancies, then send your CV to me, Martin Ivanov, Senior Recruitment Consultant for Switzerland.

Keywords: medical device, global projects, EMEA, project management, MDR, MDD, medical devices, CE-marking, CE marking, Regulatory Affairs, Regulations, FDA, QMS

Get similar jobs like these by email

By submitting your details you agree to our T&C's

Share this Job

NES Global Talent is proud to announce the strategic alignment between ourselves and the Fircroft Group to create NES Fircroft, one of the leading human capital solutions businesses for engineering and technical talent globally.