STENTiT is a medical device startup based at the High Tech Campus in Eindhoven, Netherlands, with the aim is to help people suffering from cardiovascular issues. We develop a novel class of regenerative endovascular implants for the treatment of cardiovascular diseases. Our ultimate goal is to restore the affected blood vessel from the inside out to provide a lifelong solution.
Now we are looking for our pre-clinical researcher at our Eindhoven headquarters.
This is a unique opportunity for an ambitious, multi-talented individual who wants to see the inside of a fast-moving startup and shape the development of this first-of-a-kind medical device.
You will get insights into a unique company that has the vision to become one of the world's leading players in regenerative endovascular implants.
The Pre-Clinical Researcher will assist in the planning, execution, and analysis of pre-clinical studies for the development of the company’s resorbable stent, focusing on in vivo and ex vivo testing. In this entry-level role, you will support the Pre-Clinical Affairs Manager and the broader R&D team in conducting experiments and collecting data to evaluate the safety, efficacy, and performance of the product before it advances to clinical trials. You will gain hands-on experience in pre-clinical research, contributing to critical studies that support regulatory submissions and product development. This role requires a motivated and detail-oriented individual with a strong interest in pre-clinical research and a desire to grow within the medical device industry.
Tasks
Study Support & Execution
- Assist in the preparation and execution of in vivo and ex vivo pre-clinical studies, following established protocols and guidelines.
- Set up and maintain experimental equipment, ensuring all tools and materials are ready for use in studies.
- Collect, document, and manage data from in vivo and ex vivo studies, ensuring accuracy and reliability of results.
- Assist in the analysis and interpretation of pre-clinical data, preparing preliminary reports and summaries for review by senior researchers.
Laboratory Maintenance & Compliance
- Maintain the cleanliness and organization of the laboratory, ensuring all equipment is properly calibrated and functioning.
- Follow all safety protocols and GLP (Good Laboratory Practice) guidelines, ensuring that all pre-clinical activities comply with regulatory standards.
- Assist in maintaining laboratory inventory, including ordering supplies and managing stock levels to ensure continuous operation of research activities.
Documentation & Reporting
- Accurately document all experimental procedures, observations, and results in lab notebooks and digital systems.
- Contribute to the preparation of study reports, presentations, and regulatory documents by providing accurate data and insights from conducted studies.
- Participate in team meetings, presenting data and discussing study progress with the Pre-Clinical Affairs Manager and other team members.
Collaboration & Learning
- Work closely with the Pre-Clinical Affairs Manager and other senior researchers to gain a deeper understanding of pre-clinical research methodologies.
- Engage in continuous learning by staying updated on relevant scientific literature, attending workshops, and participating in training sessions.
- Contribute to cross-functional discussions by sharing insights and asking questions to deepen your understanding of the product development process.
Support for In-Vivo and Ex-Vivo Testing
- Assist in the execution of in vivo and ex vivo tests, including preparing biological samples, setting up experiments, and monitoring test progress.
- Ensure proper handling and care of biological specimens during testing procedures, adhering to ethical guidelines and best practices.
- Support the team in analyzing results from in vivo and ex vivo tests, contributing to the overall assessment of the stent’s performance.
Requirements
Educational Background
- Higher degree in Life Sciences, Biomedical Engineering, Biology, or a related field.
- Recent graduates with relevant academic or internship experience in pre-clinical research are encouraged to apply.
- Possession of Art. 9 certificate based on Article 9 of the Experiments on Animal Act in Dutch law is highly desirable.
Experience
- Some hands-on experience in a laboratory setting, preferably involving in vivo or ex vivo testing, either through internships, academic projects, or entry-level work.
- Basic understanding of pre-clinical research principles, including biocompatibility, toxicology, and biological testing methods.
- Experience with histology (performing stainings and interpretation of stained tissues) is highly desirable.
- Experience with intravascular imaging is an advantage.
Skills & Competencies
- Strong attention to detail with the ability to accurately document and manage experimental data.
- Good organizational and time-management skills, with the ability to handle multiple tasks and projects simultaneously.
- Effective communication skills, both written and verbal, with the ability to work well within a team environment.
- A proactive and curious mindset, with a desire to learn and grow within the field of pre-clinical research.
Technical Requirements
- Basic proficiency in using laboratory equipment and software for data collection and analysis.
- Familiarity with GLP (Good Laboratory Practice) and safety protocols in a research setting is an advantage.
- Comfortable using standard office software (e.g., Microsoft Office) and willing to learn laboratory information management systems (LIMS).
Additional Requirements
- Willingness to engage in hands-on laboratory work, including handling biological specimens and working with in vivo and ex vivo models.
- Ability to work in a fast-paced, dynamic start-up environment, with flexibility and adaptability to changing priorities.
- Strong interest in contributing to innovative medical device research and a commitment to advancing healthcare solutions.
- Excellent communication skills in Dutch and English.
Benefits
- Great opportunities for personal and professional growth in a committed, innovative and dynamic team.
- Challenging and varied tasks in an innovative environment with real impact.
- Experience entrepreneurship first hand.
- Rare opportunity to actively shape the development of a first-of-a-kind medical product to safe patient lives.
Sounds interesting? We look forward to meeting you. Submit your CV and all relevant working documents online now!