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GLP Immunoanalytical Scientist - Belgium   The scope of the role is focused on supporting regulatory bioanalysis across our portfolio. This role is heavily lab based.

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Functional titles : Lab Scientist ,  Lab Analyst
Project Types : Permanent position ,
FTE : 100 %
Min.Experience : 5 year
Start Date : ASAP
End Date : N/A
Posted on : 09 February 2017

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Position filled

Project Description

The role will include but is not limited to:

  • Lab based role focused on development, validation and application of bioanalytical methods either for PK, ADA or Biomarker analysis
  • Work closely with the project bioanalytical representatives to ensure  effective  knowledge transfer of bioanalytical methods to CRO partners.
  • Collaboration with colleagues to ensure methods are appropriately validated to support GLP studies
  • Troubleshooting and resolving technical issues associated to ligand binding assays as they arise
  • Actively contribute to ensuring GLP and GCP quality systems are compliant with regulatory requirements and robust scientific practice.
  • Actively promote transfer of scientific knowledge amongst peers and keep abreast of latest developments in regulatory bioanalysis including technologies and publications.



Project FTE 100%
Work from home:   Not Allowed
No. of Positions:   1


Organization Communicative Collaboration Curiosity Interest in knowledge Problem solving Attention to detail


Analytical methods Analytical Method Validation Bioanalysis Biomarkers Pharmacokinetics CRO Good Laboratory Practice (GLP) Analytical procedures Good Clinical Practice (GCP) Regulatory Compliance ELISA MSD Pharmacodynamics Antibodies Immunology Neurology Automation

Skills and Expertise

Use laboratory techniques Analytical skills Interact with CROs Work cross-functionally Develop strong internal relationships with stakeholders Interact with regulatory stakeholders


Bachelor Master

Field of study

Biomedical Sciences (Optional)
Immunology (Optional)
Biomedical Laboratory Techniques (Optional)


Professional Proficiency
Elementary Proficiency
Good to have

Desired Skills & Experience

  • BSc./MSc. in Life Sciences (e.g. Biomedical Sciences, Medical technology, Immunology or similar)
  • A minimum of 5 years’ experience working in the pharma or CRO industry supporting regulatory bioanalysis of NBE or biomarkers programs
  • Hands-on knowledge of a range of bioanalytical techniques and platforms including but not limited to ELISA, MSD and Gyros to support the analysis of Pharmacokinetic and Pharmacodynamics endpoints including Anti-Drug Antibodies and Biomarkers.
  • Experience in autonomous method development and validation and transfer of novel methods for PK, ADA and Biomarker support.
  • Ability to troubleshoot immunoanalytical methods to ensure methods are fit for purpose.
  • Experience in working with a wide range of internal stakeholders including Non-Clinical Safety, DMPK, Translational Medicine, Clinical Pharmacology, Clinical operations and Quality Assurance colleagues.
  • Well organized, capable of communicating clear instructions to partners and stakeholders alike
  • Good knowledge of the English language both written and spoken, working knowledge of French is a plus
  • Experience utilizing automation tools such as the Hamilton Starlet or other systems would be highly desired


What we offer

Permanent contract and fringe benefits.

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