Arbetsbeskrivning

Job description

Are you an experienced Toxicology and Biocompatibility specialist looking to drive innovation and patient safety in the MedTech industry?

We are continuously seeking to connect with passionate and meticulous experts who are interested in joining our clients working with medtech products. If you thrive on ensuring the safety of ground-breaking medical devices and possess a deep understanding of global regulatory compliance, we encourage you to submit a spontaneous application.

Randstad Life Sciences is specialized in competences within Life Science. As a consultant you get a competitive salary, benefits and collective agreements. Your consultant manager ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.

Responsibilities

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.

Qualifications

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.

About the company

Randstad

At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential.

With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward.