Senior Scientist

NOVADIP-BIOSCIENCES is an innovative biotech company, based in the Walloon Region (Mont-SaintGuibert), with a strong expertise in the development of novel regenerative medicines. This human-sized structure is a leader in first-in-class treatments for bone defects and bone diseases. If you are sharing our vision of developing life-improving and life-saving products and if you are looking for new challenges amongst a dynamic and innovative team, consider collaboration with our fast growing company.

In order to support the Quality Control department, NOVADIP-BIOSCIENCES is actively looking for a:

Senior Scientist

Your main responsibilities are:

  • Participation in determining the in vitro product characterization strategy of Novadip Biosciences experimental products: scientific approach leading to definition of the product mode of action and composition; definition and justification of the analytical strategy;
  • Identification of analytical methods supporting the development and/or release needs for experimental Novadip Biosciences products.
  • Carry out technological and regulatory surveillance (EMA, FDA, ICH),
  • Organize and carry out the development, qualification and validation of analytical methods for the characterization and quality control of Novadip Biosciences products.
  • Participate in the design of studies and protocols (development, qualification and validation).
  • Collaborate with other departments, according to the needs defined in the matrix organization, principally in the context of relationships between operations departments.
  • Participate in the revision, validation and approval of analytical results, put them in context through strong scientific knowledge;
  • Manage and respect timelines
  • In collaboration with QA department, respect, put in place and verify the internal rules and procedures as well as the GLP and GMP standards


  • Master or PhD in Medical Science or related biological field
  • Minimum 5 years of experience in a similar function, preferentially in pharmaceutical industry
  • Knowledge of GLP and GMP standards
  • Rigorous, perseverant, proactive and following to the end every subject- Excellent organizational and communication skills
  • Fluent in French and English
  • Strong scientific knowledge in the field of stem cells
  • Flexibility to operate in multitasks environment


  • A full-time permanent position (40h/week) in a growing team.
  • To work in a human-sized, dynamic, respectful and professional environment.
  • The opportunity to take part in a challenging scientific and business growth.
  • An attractive salary package in line with the position responsibilities and your experience.

Please use the button above email your CV together with an adapted cover letter to Your application and related information will remain strictly confidential.