Junior QA Coordinator

Louvain-La-Neuve, Belgium

Is it time we got YOU on board? We’re proud to employ the best in the business so if you think you’re a good fit get in touch! 

CluePoints is an innovative, fast-growing company and the premier provider of Risk-Based Monitoring and Data Quality Oversight solutions to clinical research organizations. Our products enable both risk planning and operational risk monitoring and utilize advanced statistical algorithms to determine the quality of clinical trial data both during and following study execution. CluePoints is looking for exceptional individuals to help us ride the wave of growth we are seeing.

Here at CluePoints, we do things differently. We understand that a fun environment can be highly motivating and productive. When smart people work on problems, and they enjoy coming to work each day, they accomplish great things together.

If you recognize yourself in this profile and are not afraid of taking on challenges… Apply today! We are already waiting for your CV and cover letter in English.

Junior QA Coordinator

Key Responsibilities:

As QA Coordinator,  you will be responsible to:

  • Advise on quality requirements and compliance to applicable regulations
  • Ensure quality, completeness and maintenance of the Quality Management System
  • Provide input in validation and qualification activities (including risk analysis and compliance)
  • Manage internal audits/supplier audits and customer audits
  • Handle Deviations
  • Participate in the periodic review process
  • Participate in QMS performance evaluation

Skills needed:

  • Excellent English written and verbal communication skills
  • Strong interest in IT environment
  • Good interpersonal skills (communication, organizational and time management skills)
  • Team player, ability to work independently
  • Communicative, assertive, diplomatic and strive for a win-win situation
  • Ability to solve problems and to motivate others
  • Able to utilize pragmatic approach and have an eye for detail
  • Analytical, set priorities quickly, and have the sense of planning and organization

Qualifications needed:

  • Master in a health or scientific related field, Engineering or equivalent experience
  • Minimum of 1-year experience within a pharmaceutical or regulated environment or equivalent
  • Experience in the clinical research environment is a big plus
  • Experience with Computer System Validation, and regulatory requirements/guidance such as CFR 21, Eudralex, SOC2...)

Top Reasons to work with us:

  • A challenging and rewarding job in an ambitious and fast-paced technology scale-up that has received many national and international awards including “Scale-Up of the year 2019”!
  • An opportunity to work in an internationally focused, fast-growing, multi-disciplinary company and so be part of this Belgian success-story!
  • On top of that, we offer a competitive salary including a company car, within a Geek & Start-up atmosphere, some perks such as: free drinks, cookies and fruits - if you want to go the healthy road
  • A flat hierarchy
  • Last but not least: work with a great team (everyone says this, but we're serious—we're pretty great 😊)  

How to Apply

Please simply click the button on this page!

The role will be permanently based at our Belgium office. We will strictly only consider applications from candidates that are residents and/or hold valid work permit for the location they apply for.