R&D Engineer
Rapidemic
| Company | Rapidemic |
| Category | Engineering |
| Location | Leiden, South Holland, Netherlands |
| Remote | — |
| Employment | Not stated |
| Level | Not stated |
| Salary | Not stated by the employer |
| First seen | 2 Aug 2026 (the employer did not state a posting date) |
| Last verified | 10 Aug 2026 |
| Source | The employer's own careers page (company_site) |
Description
Rapidemic is seeking a Junior R&D Engineer
to join our Engineering team and contribute to the development of
next-generation in vitro diagnostic (IVD) devices. As an R&D Engineer you
will support the design, prototyping, characterization, and verification of
integrated diagnostic systems spanning fluidics, thermal management, optics,
electronics, and consumable components. This is a hands-on role suited to a
detail-oriented, early-career engineer who thrives in a fast-paced,
multidisciplinary environment and is eager to grow technical depth across
hardware development and design controls within a regulated medical device
setting (ISO 13485). You will work alongside experienced engineers, and scientists,
gaining direct exposure to the full development lifecycle from concept
exploration to design transfer. Job Title: R&D Biomedical Engineer
Level: Junior
Reports to: Head of Engineering
Type: Full-time position (40h/week).
Location: BioPartner 3, Leiden Bioscience Park, Zuid-Holland.
Modality: On-site. 1 day/week remote possible.
Contract: Temporary, 1 year contract with possible extension
Start Date: As soon as possible. Latest August 2026
Support
with the design and prototyping of IVD device subsystems and consumables,
including mechanical, fluidic, thermal, and electromechanical components.
Build,
assemble, and iterate on engineering prototypes in the lab; perform
hands-on testing using standard and custom lab equipment.
Plan
and execute design verification experiments, including writing test
protocols, collecting and analyzing data, and producing clear technical
reports.
Generate
and maintain CAD models, engineering drawings, and technical documentation
in line with internal design control procedures.
Support
failure analysis, root cause investigation, and design iterations based on
experimental and field feedback.
Work
cross-functionally with other teams to integrate subsystems into products.
Maintain
accurate records in the design history file (DHF) and contribute to risk
management activities (ISO 14971) under the guidance of senior engineers.
Help
maintain a safe, organized, and productive lab environment.
Participate
in project meetings, contribute ideas, and present findings.
Educational
Background:
B.S.
or M.S. degree in Mechanical, Biomedical, Chemical Engineering, Applied Physics,
or closely related disciplines.
0-2
years of relevant experience (internship, thesis project, and student
team work count); we welcome applications from recent graduates.
Required
Skills:
Solid
foundation in engineering fundamental; mechanics, heat transfer, fluid
dynamics, or basic electronics.
Hands-on
prototyping skills: experience with at least one CAD software
(SolidWorks, Fusion 360, or equivalent), 3D printing, basic machining,
soldering, or breadboarding.
Comfortable
with experimental work, defining test setups, executing measurements, and
interpreting data.
Strong
with data analysis and scientific data analysis tools (Python, MATLAB, or
equivalent) and standard office tools.
Strong
written and verbal communication in English; ability to produce clear,
structured technical documentation.
Curious,
methodical, and self-driven; able to work independently on well-scoped
tasks while collaborating effectively in a small team.Excellent
verbal and written communication in English.
Attention
to detail and a proactive attitude.
Preferred
Skills:
Experience
with medical device development, IVDs, or other regulated environments
(ISO 13485, IEC 62366, IEC 61010, IEC 60601, or IVDR/FDA frameworks).
Familiarity
with design controls, risk management (ISO 14971), and verification &
validation methodology.
Experience
with one or more of: microfluidics, low-volume liquid handling, thermal
control systems, or embedded electronics.
Knowledge
of statistics for engineering (DOE, GR&R, capability analysis);
coursework or certification (Six Sigma Green Belt) is a plus.
Familiarity
with molecular biology workflows at a conceptual level. Sufficient to
communicate effectively with assay team members.
Experience
with version-controlled documentation, PLM systems, or electronic QMS
tools.
Awareness/exposure to design for manufacturing (DFM) and design for assembly (DFA)
principles.
A
competitive salary.
An
incredible learning experience working in a growing start-up.
A
relaxed work atmosphere.
The
opportunity to explore and test your own ideas.
A
working experience in a European hub for life sciences innovation.
A
work experience in the diagnostics industry.
Please apply only if you can realistically be physically in Leiden and start before August 2026.If you believe you are the person we are looking for, then we look forward to receiving your applications before the 30th of May. Only applications submitted via this portal will be considered.