Verification and Compliance Ingénieur (m/f/d) — Coopers Group AG
- Lieu
- Zug
- Contrat
- contracting
- Publié
- il y a 6 jours
Vue d’ensemble du poste
In this role, you will be responsible for the independent regulatory verification and evaluation of third-party products (3rd party products) in relation to the applicable European (EU-MDR / EU- IVDR) and Swiss regulations (MedDO / IvDV).
- In this role, you will be responsible for the independent regulatory verification and evaluation of third-party products (3rd party products) in relation to the applicable European (EU-MDR / EU- IVDR) and Swiss regulations (MedDO / IvDV).
- Regulatory verification: Independent review and evaluation of technical documentation, declarations of conformity (DoC), CE certificates and markings of 3rd party medical devices and in vitro diagnostics, verification of the correct labeling with regard to CH-REP (Swiss Authorized Representative) and importer obligations according to MedDO/IvDO.
- Vendor & Partner Management: Communication with suppliers and partners to demand, review and clarify missing regulatory evidence and quality agreements.
- Life Sciences - Quality Management Contracting Full Time
- As soon as possible/latest start date 1.11.2026 - 6 months Compliance, IVD, Medtech
Responsabilités principales
- Regulatory verification: Independent review and evaluation of technical documentation, declarations of conformity (DoC), CE certificates and markings of 3rd party medical devices and in vitro diagnostics, verification of the correct labeling with regard to CH-REP (Swiss Authorized Representative) and importer obligations according to MedDO/IvDO.
- Vendor & Partner Management: Communication with suppliers and partners to demand, review and clarify missing regulatory evidence and quality agreements.
- PRRC Support: Creation of recommendations for the release or blocking of third-party products for the Swiss market.
- Operational support in the area of regulatory as required: e.g. supplier enquiries, document review (non-exhaustive list) Must Haves:
- Successfully completed studies in the field of medical technology, natural sciences, industrial engineering or a comparable qualification
- Fluent in German and English, both written and spoken
- Regulatory expertise: Demonstrable, several years (3+ years) of professional experience in Regulatory Affairs / Quality Management in the medtech or IVD sector In-depth knowledge
- Focus: Swiss In-vitro Diagnostics Ordinance (IvDV) Swiss Medical Devices Ordinance (MedDO)
- Experience with 3rd party processes: Hands-on experience in auditing, approving or verifying supplier and third-party documentation Job profile Life Sciences Quality Management Zug Contracting Full Time
- As soon as possible/latest start date 1.11.2026
Exigences principales
- Life Sciences - Quality Management Contracting Full Time
- As soon as possible/latest start date 1.11.2026 - 6 months Compliance, IVD, Medtech
Détails supplémentaires
- Operational support in the area of regulatory as required: e.g. supplier enquiries, document review (non-exhaustive list)
- Regulatory expertise: Demonstrable, several years (3+ years) of professional experience in Regulatory Affairs / Quality Management in the medtech or IVD sector In-depth knowledge
- Focus: Swiss In-vitro Diagnostics Ordinance (IvDV) Swiss Medical Devices Ordinance (MedDO)
- Experience with 3rd party processes: Hands-on experience in auditing, approving or verifying supplier and third-party documentation Quality Management Compliance, IVD, Medtech
Notes et contenu original
- Responsibilities:
- Must Haves:
- Regulatory expertise: Demonstrable, several years (3+ years) of professional experience in Regulatory Affairs / Quality Management in the medtech or IVD sector
- In-depth knowledge
- Focus: Swiss In-vitro Diagnostics Ordinance (IvDV)
- Swiss Medical Devices Ordinance (MedDO)
- Experience with 3rd party processes: Hands-on experience in auditing, approving or verifying supplier and third-party documentation
- Job profile
- Life Sciences
- Quality Management
Questions sur cette offre
Quel salaire propose Coopers Group AG pour ce poste ?
Coopers Group AG indique CHF 78 500 - 119 000 bruts par an pour ce poste à Zug. Il s'agit du salaire publié dans l'annonce d'origine (ou, si l'employeur ne précise pas de montant, d'une estimation réaliste pour le rôle et le secteur) — le calculateur de ce site le convertit en net réel une fois l'impôt frontalier et les cotisations sociales appliqués.
Est-ce un poste à temps plein, et quel type de contrat propose Coopers Group AG ?
Cette offre est un poste en temps plein. Le type de contrat affiché ici provient directement de l'annonce originale de l'employeur ; confirmez toujours les horaires exacts, le préavis et la durée d'essai avec Coopers Group AG pendant le processus de candidature, ces détails pouvant varier même au sein de la même catégorie de contrat.
Ai-je besoin d'un permis de frontalier pour un poste dans le canton de Zoug ?
Les résidents UE/AELE domiciliés dans la zone frontalière du pays voisin du canton de Zoug peuvent demander un permis G ; l'employeur suisse le dépose auprès de l'office cantonal des migrations après signature du contrat. Les règles de zone frontalière et les délais varient selon le pays voisin et le canton — confirmez les détails auprès de l'office des migrations du canton de Zoug ou avec les RH pendant la candidature.
Comment postuler à ce poste chez Coopers Group AG ?
Utilisez le bouton « Postuler maintenant » sur cette page — il renvoie directement à l'annonce originale de Coopers Group AG sur coopers.ch, votre candidature arrive donc directement dans le système de suivi des candidatures de l'employeur. Frontaliere Ticino ne collecte ni ne transmet lui-même les candidatures.
