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18,000+ live jobsClinical Chemist (Consultant)
On-site in Groningen·Part-time·Added 5 days ago (last checked 21 Oct)
Our summary
- Work mode
- On-site, Groningen
- Contract
- Part-time
- Languages
- Dutch



This job advert was originally written in Dutch.
Requirements
What we're looking for
An experienced clinical chemist or a similarly qualified professional within clinical laboratory diagnostics, with extensive expertise in the fields of clinical chemistry, hematology, coagulation studies, serology, and urinalysis.
Experience with ISO 15189, laboratory accreditation, and quality systems.
Experience with method validation and the interpretation of clinical laboratory results.
Appropriate professional education, qualifications, and/or registration that align with the scope of the position.
Experience with clinical studies or within the pharmaceutical industry is a plus.
The role
Clinical Chemist (Consultant)
Location: Groningen, Netherlands
Type of collaboration: On a consultancy basis, with more intensive involvement during the startup phase of the laboratory.
What you'll do
Providing scientific and medical supervision of laboratory research and monitoring quality.
Guiding method validation and the introduction of new assays.
Reviewing and approving important laboratory procedures and documentation.
Supporting ISO 15189 accreditation and audits, and advising on compliance with relevant laws and regulations.
Providing scientific advice on protocols, complex laboratory results, and answering client questions.
Advising on laboratory strategy, technology, and future testing capabilities.
Collaborating with the Laboratory Manager to ensure compliance with relevant scientific and quality standards
About the role
In Groningen, QPS NL is setting up a new Central Safety Laboratory to support clinical studies with high-quality clinical laboratory diagnostics. For this purpose, we are looking for an experienced clinical chemist who will provide scientific and technical supervision for the setup and further development of the laboratory. This is an advisory role (not a position focused on daily operational management). In this role, you will work closely with our Lab Manager, who is responsible for the daily operations of the laboratory.
Expected duration
In this advisory role, we expect the commitment to vary per phase:
Startup phase: approximately 10-15 hours per week
During the first operational phase: +/- 8 hours per week
Once the laboratory is fully operational: +/- 4 hours per month
Interested?
Interested?
Are you interested in contributing your expertise to the development of a new Central Safety Laboratory, while maintaining flexible consultancy involvement? Then we would love to get in touch with you!
Ready to apply?
Ready to apply? Send your CV to HRM.NL@qps.com or apply via our careers page at www.qps.com.
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