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Compliance Manager (m/w) - Luzern - Global Medical Device

Posted on Apr 24, 2020 by NES IT

Luzern, Switzerland
Engineering
Immediate Start
Annual Salary
Full-Time
Compliance Manager (m/w) - Luzern - Global Medical Device Company

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.

Within our range of clients we support big and small players in the industry who are leading organisations that manufacture products for the local and global markets. Their upcoming and current projects require a professional at their site in Luzern and they've reached to us for our support. In order to strengthen their team we are looking for a Compliance professional to join them.

Responsibilities:
  • Coordination of qualification and validation activities
  • Maintenance of and compliance with specific validation master plans
  • Coordination of the required risk analyses
  • Proactive support in the preparation of qualification the building infrastructure and related documents
  • Compliance with registration requirements and conditions for medicinal products and medical devices
Requirements:
  • Scientific university/technical degree in engineering, chemistry, biology, microbiology, pharmacy
  • Several years of professional experience in the field of pharma products or medical device manufacturing as well as several years of experience in validation/qualification activities and document management
  • Sound knowledge of cGMP, ISO 13485 requirements, risk analysis and data integrity
  • Expertise in quality management and statistical methods
  • Flair for technical and constructional connections with experience in project management
  • Very good knowledge of German, English is an advantage
  • Secure handling of MS Office
What to expect:
  • Detailed conversation and introduction to all roles and clients 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
Notes: The responsibilities may differ depending on our clients' needs

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 at (see below)

Keywords: medical device, quality engineering, global projects, management, MDR, MDD, medical devices, project management, PM, EMEA, FMEA, Risk, Risk management, Engineering, FDA

Established in 1978, NES Global Talent provides a complete range of contract and permanent talent solutions to the Oil and Gas, Power, Construction and Infrastructure, Life Sciences, Manufacturing and IT sectors worldwide. With more than 40 offices in 28 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. Offering far more than a traditional recruitment service, we fully support our contractors while they are on assignment with everything from securing visas and work permits, to providing market leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.

Reference: 882784445

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