Regulatory Affairs Specialist

🔎 Title: Regulatory Affairs Specialist

📍 Location: Vaud, Switzerland, hybrid, 2-3 days on site per week

⏳ Contract: 12 months, full time

✉️ Contact: emma@elemed.eu

✅ Mandatory experience: CE marking of consumer electrical appliances (Low Voltage Directive and EMC Directive)

Do you want to own the regulatory work for a range of wellness appliances across EMEA, from the first test reports to the label on the box?

🔸 The company

This is an international consumer products company with a portfolio of well-established brands sold across many markets. Its regional office for EMEA is based in Vaud.

The business is growing its range across EMEA, and this role has been created to support that growth. Regional leadership is closely involved, so decisions are made quickly and your work is visible from day one.

You’ll join a small Quality and Regulatory team. Each regulatory specialist owns a product category, and the team also includes compliance and quality colleagues. Each specialist works directly with their own marketing and development teams, and the whole team regularly shares processes, knowledge and ways of working with each other.

🔹 The Opportunity

You’ll cover the full product lifecycle: working with development on compliance and testing, compiling technical documentation, maintaining CE marking and the EU Declarations of Conformity, and reviewing labelling and marketing materials with the marketing team.

Many regulatory roles in regional head offices are mostly administrative. In this one you’ll be involved from development through to market. The rest of your time goes on supporting other product categories, as well as notifications and registrations for EMEA.

🔸 Your responsibilities:

• Maintain regulatory documentation to keep the EMEA product portfolio compliant, including CE marking
• Compile and maintain technical documentation for timely approvals, registrations and ongoing market compliance
• Prepare and maintain EU Declarations of Conformity
• Own labelling review, including marketing materials, with support for other categories where needed

🔸 What you’ll bring:

• At least 2-3 years in regulatory affairs for consumer electrical appliances, ideally in the EMEA region
• Hands-on CE marking experience under the Low Voltage Directive and EMC Directive
• Knowledge of WEEE, REACH and RoHS, with CLP classification and labelling experience a big plus
• Working knowledge of ISO 13485 and/or ISO 9001
• Fluent English
• Packaging regulation (PPWR) knowledge is a bonus

✉️ If you are interested in this role, please send your application directly to emma@elemed.eu

Please note: Due to the high volume of applications we sometimes receive, our team might not be able to contact each applicant individually regarding the status of their application. If you do not hear from us after 10 days, please consider your application unsuccessful.