Medical Technologist - Molecular

☞ Medpace

View: 130

Update day: 29-11-2025

Location: Leuven Flemish Brabant

Category: R & D IT - Software

Industry: Pharmaceutical Manufacturing

Position: Mid-Senior level

Job type: Full-time

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Job content

Job Summary

The Medical Technologist Molecularat Medpace Reference Laboratories plays a pivotal role in research based drug development within the pharmaceutical industry. Due to our recent growth, we are in need of qualified and focused driven individuals, like yourself. You would have the unique opportunity to work on the laboratory side of the fast paced medical world by conducting tests on blood, urine, tissue and other samples. If you have an analytical mind set, and enjoy working in a laboratory setting, this could be the opportunity for you!

Responsibilities
  • Perform routine instrument maintenance and troubleshooting;
  • Expected to develop knowledge of federal regulations regarding clinical trials;
  • Expected to develop knowledge of pre-analytical variables affecting clinical laboratory testing;
  • Expected to develop knowledge of disease processes and correlation with clinical laboratory data;
  • Perform laboratory investigations;
  • Perform testing, documentation, and routine lab system operations;
  • Ensure validity of laboratory data reported, and
  • Working in rotation schedule: Monday - Friday and Tuesday – Saturday.

Qualifications
  • Bachelor or Master Science degree in molecular biology, genomics or equivalent and at least 1 year of laboratory experience;
  • MT(ASCP), MLS(ASCP), or CLS(NCA) certification (if applicable);
  • Familiarity with basic molecular biology techniques (PCR, RT-PCR);
  • Good theoretical and practical knowledge of Sanger sequencing and Next Generation sequencing techniques;
  • Good molecular practical experience including qPCR, Sanger Sequencing and Next generation Sequencing is a plus;
  • Laboratory experience of DNA/RNA sequencing, using Sanger sequencing and Next Generation Sequencing;
  • Excellent written and verbal communication skills and good command of both written and spoken of English;
  • Able to work in a team environment with effective interpersonal skills and able to work independently.

We kindly ask to send applications in English.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Today

The work we’ve done over the past 30 years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Awards:
  • Recognized by Forbes as one of America’s Best Mid-size Companies in 2021 and 2022
  • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next:

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
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Deadline: 13-01-2026

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