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Open Positions

Shape the future of the healthcare industry
Do you want to help us shape the future of the healthcare industry? Check out our open positions and join us on our mission to turn this challenge into an opportunity with continuous patient monitoring.

Clinical Research & Operations Specialist (Dutch-Speaking)

Location:

Netherlands (Hybrid options available)

Start Date:

April 2024

Commitment:

4-5 days per week

Experience:

1-2 years

Field:

Clinical Research, Biomedical Sciences, Technical Medicine, Medicine, or related
Corsano Health is looking for an enthusiastic and proactive Clinical Research & Operations Specialist to start in April at our dynamic office at The Hague Tech. This is an exciting opportunity for someone eager to gain hands-on experience in the rapidly evolving Med-Tech industry. If you're passionate about managing clinical trials, supporting clients, writing grant proposals, and playing a key role in operational tasks, this is the perfect chance to make an impact!

Corsano Health is at the forefront of developing, producing, and selling medically certified wearables for continuous vital sign monitoring. Our flagship product, the Corsano Solution, is a CE-MDR-certified and FDA-cleared system designed to monitor vitals such as heart rate, blood pressure, respiratory rate, saturation, temperature, and activity.

 As a Clinical Research & Operations Specialist, you will be the first point of contact for our clients, building strong relationships and providing top-tier support. You’ll work closely with cross-functional teams, including developers, production staff, and clinical trial coordinators, to deliver optimal service to our clients. You will also play an important role in clinical tasks, such as supporting clinical trials, applying for research grants, and overseeing logistics, including inventory management, orders, and mail.

 At Corsano, we offer you a varied and engaging role within a fast-growing scale-up environment that blends innovation with healthcare. You will gain valuable experience in international clinical trials, collaborate with hospitals and research institutions, and have the opportunity to attend inspiring (online) events in the Med-Tech field.

Key Responsibilities:

• Oversee the management of clinical trials, ensuring compliance and efficiency.
• Prepare and submit grant proposals to secure research funding.
• Handle METC submissions and approval processes.
• Write and publish scientific articles sharing results from clinical trials.
• Act as a customer service representative, including meetings with potential clients, addressing inquiries, logistics, and troubleshooting.
• Explain the capabilities of the Corsano Bracelet to potential customers.
• Represent the company at conferences and industry meetings.

Who We're Looking For:

• Fluency in both Dutch and English (spoken and written).
• 1-2 years of work experience, preferably in clinical research, trials, or grant writing.
• Experience with grant proposal writing, or willingness to develop expertise in this area.
• Strong understanding of clinical trial operations and regulations, or an eagerness to learn.
• Experience in customer-facing roles, including client communication and problem-solving, or eager to learn.
• Strong organizational and writing skills, with a keen attention to detail.

Proactive and independent, with the ability to take initiative and manage multiple tasks effectively.

What We Offer:

• Opportunity to work on cutting-edge clinical research and gain international exposure.
• Collaboration with hospitals, research institutions, and industry experts.
• A dynamic, supportive team environment within a scale-up company that operates in healthcare.
• Access to inspiring (online) events in the Med-Tech field, providing learning and networking opportunities.

If you’re excited to make an impact in the Med-Tech world and advance your career in clinical research and operations through a fast-paced and rewarding role, we’d love to hear from you!

 

How to Apply:
Please apply by contacting Beatrice Gagliostri at
beatrice.gagliostri@corsano.com
. Send your CV (in English) by March 24th along with a brief explanation of your motivation in English.
Quality Assurance Engineer (QA)

Location:

 Corsano Health, Geneva or The Hague

Job Type:

 Full-Time

About Corsano Health:

 Corsano Health is at the forefront of developing, producing, and selling medically certified wearables for continuous vital sign monitoring. Our flagship product, the Corsano Solution, is a CE MDR certified and FDA Cleard system designed to monitor a.o. pulse rate, blood pressure, respiratory rate, SpO2, temperature and activity. We are committed to innovation and excellence in the medtech sector, and we are looking for a talented QARA Manager to join our dynamic team.

Job Description:

 Corsano Health is seeking a

hands-on QA Engineer

to Implement & maintain the Quality Management System (QMS) is compliant with 

ISO 13485

 and 

EU Medical Device Regulation (MDR)

 requirements. The QA Engineer will be responsible for maintaining and improving our Quality Management System (QMS) to ensure compliance with regulatory standards. You will work closely with cross-functional teams, including software developers and product managers, to manage quality processes and documentation for medical device development. This position reports to the COO.

Key Responsibilities:

1) Quality Management System (QMS):

• Maintain and improve the QMS in compliance with ISO 13485 standards and CE MDR requirements.
• Ensure all QMS-related documentation is up-to-date and properly controlled.
• Lead internal audits and support external audits.

2) Documentation Management:

• Follow up with developers and other teams to ensure timely completion of SRS (Software Requirements Specifications), SDS (Software Design Specifications), test reports, and other technical documents.
• Review, update, and manage technical files and design history files.
• Follow up and ensure timely completion of the Feedback Register to comply with Post-Market Surveillance (PMS)requirements, addressing customer feedback, incidents, and field performance data.Ensure traceability and version control of all documentation.
• Ensure traceability and version control of all documentation.

3) Process Improvement:

• Identify and implement process improvements to enhance efficiency and compliance.
• Provide training to the team on quality and regulatory processes.

4) Product Testing and Validation:

• Support verification and validation activities.
• Ensure test protocols and reports are properly documented and aligned with standards.

Qualifications:

• Bachelor’s degree in Engineering, in the field of life sciences / technical or medical devices; preferably knowledge of electronic devices (hardware, software and firmware).
• 3+ years of experience in quality assurance within the medical device industry.
• Strong knowledge of 

ISO 13485

and 

CE MDR

.

• Experience with software as a medical device (IEC 62304) is a strong advantage.
• Familiarity with FDA 21 CFR Part 820 is a plus.
• Hands-on experience in a startup or scale-up environment is highly desirable.
• Proficiency with document control systems and QMS software.
• Strong attention to detail and organizational skills.
• Excellent communication and collaboration skills.
• Fluency in English (written & spoken).

Benefits:

• Competitive Compensation: Attractive salary and performance-based incentives, aligned with company growth and leadership progression.
• Professional Development: Access to leadership training, industry conferences, and a network of seasoned mentors to support your growth.
• Innovative Work Environment: Join a cutting-edge, mission-driven company that fosters collaboration, creativity, and continuous improvement.

This is an exciting opportunity to join a fast-growing HealthTech company at a pivotal moment of expansion. As
QA
Engineer
, you will play a key role in ensuring regulatory compliance and maintaining the highest quality standards for innovative healthcare solutions. Your expertise will drive regulatory strategies, shape the Quality Management System, and help bring life-changing technologies to market. This role offers the chance to make a meaningful impact while advancing your career in a dynamic, mission-driven environment.

How to Apply:

 Interested candidates are invited to submit their resume and a cover letter detailing their relevant experience and why they are a great fit for this role to info@corsano.com. Please include "QA Engineer" in the subject line.

Corsano Health is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Data Scientist Intern
Corsano Health is looking for an enthusiastic and dynamic 
Data Scientist Intern
 for our Yes!Delft office in The Hague. Reporting to the Chief Medical Officer, the Data Scientist works with users to define existing or new processes as well as to recommend solutions and improvements. The candidate needs to have strong project management skills and the ability to work independently, creatively and analytically in a problem-solving environment.

The position can start as a part-time commitment. Initially expected working hours are 8 hours per week. Pay will be commensurate with attitude, experience and hustle.

Your Impact

• Work with users to define existing or new processes and recommend solutions and improvements. Serve as a liaison between users needs and the Strategic Improvement Department.
• Develop test plans and verify plans to accurately validate business requirements.
• Develop project work plans.
• Documen

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