toxicologist.

This is not an advertisement for a single, immediate opening, but an invitation to connect with us for future potential employment and consulting opportunities as our client base expands and new projects are secured.

The length, scope, and exact responsibilities of assignments vary depending on the client and the specific role. Since this is a spontaneous application to cover future needs, we have not set a specific assignment length, but on average, assignments last for about 6 months.

Essential requirements:

• Education: A Master’s or Bachelor’s degree in Engineering, Chemistry, Life Science, or a closely related field.
• Expertise: Extensive experience in biocompatibility, toxicology, or a closely related field, specifically within the development of medical devices.
• Regulatory Knowledge: Strong knowledge of national and international regulatory requirements relevant to biocompatibility (e.g., ISO 10993 series).
• Communication: Excellent communication skills, fluent in both written and spoken English.

Highly desirable skills:

• Experience in supporting major regulatory submissions and filings (e.g., FDA, MDR/CE Mark).
• Familiarity with robust design control processes in a MedTech environment.
• Proven leadership skills demonstrated through mentoring or coaching colleagues.
• Experience in scientific or medical writing.