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Open nowPosted 2 days ago

Regulatory Affairs Specialist (ZZP)

EURES job mobility portal612,521 open roles

Where
Noordoost-Noord-Brabant, Netherlands
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Your applicationOpen nowRegulatory Affairs Specialist (ZZP)EURES job mobility portal · Noordoost-Noord-Brabant, Netherlands
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Early applications get read.

10.7% of postings close within 7 days. Measured by our own scanner across the market. EURES job mobility portal postings stay open a median of 9 days.

Share of postings closed within
  1. 2.0%1 day
  2. 4.4%3 days
  3. 10.7%7 days
  4. 16.1%14 days
  5. 34.1%30 days
This job: posted 2 days ago

EURES job mobility portal median: 9 days open

The posting

Getnoticed logo Interim Regulatory Affairs Specialist (ZZP) Remove as favorite Favorite Favorite Getnoticed logo Language EN FR ES Getnoticed logo Own your expertise At Nutreco, passionate and curious experts with diverse backgrounds unite to Feed the Future. Interim Regulatory Affairs Specialist (ZZP) Quality Trouw Nutrition Remove as favorite Favorite Favorite - Boxmeer - Part time - Quality Apply to this job Interim Regulatory Affairs Specialist (ZZP) Job Description - Duration : Initial assignment of 3 months - Hours : 24-32 hours per week - Contract Type : Interim assignment for an independent professional (ZZP) - Location : Boxmeer (hybrid), with office presence expected approximately once per week Own the detail that helps products reach customers around the world. As an Interim Regulatory Affairs Specialist, you will independently coordinate product registration and regulatory documentation activities across our export business. Partnering with stakeholders across multiple countries, you will help ensure the timely completion of registration, renewal and documentation requirements in export markets throughout the Middle East and Africa. Our Export business supports customers across the Middle East and Africa with animal nutrition products manufactured through a network of Nutreco companies and external production partners. Operating across multiple countries means navigating different registration requirements and compliance expectations. As part of the Quality & Regulatory Affairs team, you will work in an international business-to-business environment where attention to detail and stakeholder management are key to success. What you'll do - Coordinate and manage product registration, renewal and re-registration activities across export markets. - Prepare, review and maintain regulatory dossiers and supporting documentation. - Coordinate regulatory documentation requests from customers, authoritie...

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