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Laboratory Technician & Study Director Assistant W/M

NAMSA Medanex Clinic -
Diest

Postuler rapidement

Détails de l'emploi

CDD
Il y a 3 jours

Qualifications

Microsoft Office
Bachelier
Smartsheet
IT
Collecte de données

Description complète du poste

NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976.

We are shaping the industry. NAMSA has been a key contributor to the development of the test methods that govern our industry. We have become the industry’s premier provider. We provide support for clients during every step of the product development lifecycle and beyond.

Come and work for an organization with the:

Vision to inspire innovative MedTech solutions that advance global healthcare, improve patient lives and accelerate Client success and the

Mission to deliver best-in-class global MedTech development solutions through our people, expertise and technology by adhering to our core

Values:

Act with integrity in everything we do.
Provide best-in-class customer experiences.
Develop superior talent and deliver expertise.
Respond with agility and provide timely results.
Embrace collaboration, diverse perspectives and ideas.

Job Description:

Primarily involved in various testing activities in accordance with SOPs, and utilizing applicable work instructions, standards or guidelines.
May be responsible for extractions, test article and control preparation, solution preparation.
Clean glassware and prepare reagents for use in laboratory testing.
Perform routine disposal of laboratory waste including disposal of test articles.
May be responsible for chain of custody, delivery of samples, filing and sample distribution/shipping.
Accurately collect and record raw data in logbooks and on worksheets.
Review raw materials and final finished media for conformance with applicable material specifications and SOPs.
Maintain clean workspace, testing supplies, and equipment.
May be responsible for checking laboratory equipment and respond to continuous monitoring alarms. If needed, the associate will respond in accordance with criteria outlined in Standard Operating Procedures.
Will be required to operate specified laboratory equipment.

Assists Study Directors with all aspects of preclinical animal studies
Assists in step up of animal studies, including planning, ordering, and preparing of materials and paperwork
Assists with data collection, documentation and analysis, data review (QC), database entry, and generating data
Assists with the reporting of study results
Assists with archiving of study records and materials
Handles logistical responsibilities as they relate to client materials inventory, specimen shipment, and documents, including the maintenance of accurate chain of custody documentation
Reviews related documents for consistency and regulatory compliance.
Interacts as needed with clients, auditors, inspectors, subcontractors, consultants, and other individuals or departments.
Provides clerical/administrative assistance to general facility management
Ensures compliance with Good Laboratory Practices (GLP) standards
Other duties as assigned.

Qualifications & Technical Competencies:

Your Laboratory Technician duties will be the following :

Preparing and performing routine blood (hematology, biochemistry, coagulation, ELISA, …)

and urine tests.

Lab and clinical data management (input, processing, reporting).

Managing laboratory and clinical equipment (validations, software updates, calibrations, maintenance, periodic quality checks).

Maintenance of the lab (orders and purchases, quality controls, maintaining inventory).

Compliance with GLP regulations.

Occasional participation in the weekend rotation.

Your Study Director Assistant duties will be the following :

Assist the preclinical Study Directors:

Set-up: planning, ordering, preparing materials and paperwork

Conduct, follow-up & data management: data collection, documentation and analysis, data review (QC), database entry and generating/tabulating data

Reporting of study results

Archiving of study records and materials

Logistical responsibilities: maintenance of client materials inventory, shipment of specimens, maintaining accurate chain of custody documentation, …

Comply with GLP regulations and ensure GLP standards are met.

Your qualifications:

Bachelor’s degree in a related field, e.g., agro- and biotechnology, (bio)chemistry, medical laboratory technology, veterinary technology or other relevant disciplines.

Experience with GLP or other quality systems is an asset but not a must.

You are dedicated to your tasks, precise and perfectionist, eager to learn, willing to invest time in your learning process and flexible in switching between tasks.

Team player with a hands-on mentality and proactive approach.

You are proficient in English.

Advanced IT skills, working with different tools such as MS Office, Smartsheet, Labware.

Why you should apply:

A 6-month fixed-term contract starting in October 2026 with the possibility to extend, depending on performance and business needs

A challenging and varied role in a globally expanding company

A highly professional team and an international working environment

An attractive remuneration package

Please upload your CV and Motivation letter (in English) via our NAMSA Careers website.

Don’t hesitate to contact us on +32 13 67 35 00 for further information.

Postuler rapidement

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