From Strategy to international Approval.

You develop regulatory strategies for our electrical devices, coordinate international product registrations, and manage them throughout the entire product lifecycle.

Your role

You will support the implementation of regulatory requirements for our electrical equipment (ovens, milling machines, etc.) and share responsibility for creating and maintaining national and international technical documentation.
Together with Product Development, Sales, and Marketing, you will develop the regulatory approval strategy, successfully implement it, and reliably manage deadlines and timelines.
You will coordinate international product registrations—from new registrations and amendments to deregistration—in collaboration with subsidiaries, local partners, and regulatory authorities.
You will use your expertise to support other departments with complaints, Non-Conformities (NCs), and Corrective and Preventive Actions (CAPA).
You will monitor regulatory developments and assess the impact of changes on registrations.
You will work as part of project teams.

Your profile

Bachelor’s degree in medical technology, electrical engineering, electronics, mechanical engineering, or a comparable qualification
Several years of experience in regulatory affairs for electrical devices and medical devices is a plus
In-depth knowledge of regulatory requirements for electrical devices, machinery, and medical devices, as well as international approval requirements, is desired
A structured, independent work style and a passion for cross-functional collaboration
A pragmatic approach and a strong focus on finding solutions
Excellent German and English language skills, additional languages are a plus

What we offer

A global, purpose-driven company with 3,700 employees.
A culture of innovation and collaboration.
Learning and development tailored to your growth.
Attractive benefits.

For this full-time position (40 hours per week), the gross annual salary starts at 44,000 EUR and a variable bonus based on the company's earnings. Actual compensation will be determined based on professional qualifications, relevant work experience, and the skills required for the position. Salary classification is in accordance with the applicable working agreement for the rubber and plastics processing industry.

Information at a Glance

Work location: Naturns, Italy

Business Area: Quality & Regulatory

Workload: 100%

Contract type: Permanent

Experience level: Entry Level

Recruiter Contact Details: Oliver Moser, Oliver.Moser@ivoclar.com, +39 0473 670 109

Ready to Make an Impact?

Apply now and help us bring dental innovation to life.