Company Description
About Avery Dennison
Avery Dennison Corporation (NYSE: AVY) is a global materials science and digital identification solutions company. We are Making Possible™ products and solutions that help advance the industries we serve, providing branding and information solutions that optimize labor and supply chain efficiency, reduce waste, advance sustainability, circularity and transparency, and better connect brands and consumers. We design and develop labeling and functional materials, radio-frequency identification (RFID) inlays and tags, software applications that connect the physical and digital, and offerings that enhance branded packaging and carry or display information that improves the customer experience. Serving industries worldwide — including home and personal care, apparel, general retail, e-commerce, logistics, food and grocery, pharmaceuticals and automotive — we employ approximately 35,000 employees in more than 50 countries. Our reported sales in 2024 were $8.8 billion. Learn more at www.averydennison.com.
Avery Dennison is an equal opportunity employer.
Please let us know if we can support you with reasonable accommodations throughout the application process by contacting our team via Requestaccomodation@eu.averydennison.com.
Job Description
Are you interested in working in a manufacturing company and learning more about product safety, regulatory compliance, and risk assessment in a changing and dynamic environment? Then apply now!
As Regulatory Coordinator within our Product Compliance Intern team, you will gain a deeper insight into the regulatory requirements of the customers we are serving. In addition, you could also choose to actively partake in our regulatory project related to safety, business, and socioeconomic assessment within the Label and Graphic Materials portfolio.
Your main tasks will be the following:
We would be looking for candidates seeking experience- and/or project-based internship. For project-based internships, this position can be tailored to support our regulatory assessment/ benchmarking. In this case, we would be interested in candidates who have experiences in medical, biomedical, pharmaceutical, toxicology, and related business degrees afterwards. The objective of your project is tailored to provide regulatory analyses on various layers of medical devices/pharma regulation and its interaction with healthcare industries/society.
The preferred start date is June 15th 2025, or earlier. The ideal candidate is available for 5 days a week for at least 6 months. The location of the position is our European Headquarters in Oegstgeest. The internship can be done hybrid with prior arrangement.
Qualifications
What kind of candidate are we looking for?
Additional Information
Our offer
Important: Only applications in English will be considered! Applicants need to be enrolled at a Dutch university for the whole duration of the internship.
Note: We do not accept unsolicited referrals or resumes from any source other than directly from candidates using their personal email addresses.
Read Full Description