Offres d’emploi

InoKura is a company with more than 40 years of experience in conducting early phase clinical trials, especially Phase I and IIa clinical trials. Our mission is to safely assess new pharmaceutical compounds with our experience in this field. Clinical studies are driven by a collaborative approach that assembles the whole team’s skillset around each project.

InoKura is located in the University Hospital of Liège (Sart-Tilman).

For more information, visit our website : https://www.inokura.be/

As part of the InoKura team :

You will lead the QA system and team in place. In collaboration with the General Management, you will ensure that continuous improvement is made and that a high level of quality is maintained in terms of processes, documentation, monitoring, etc. in all the company’s departments.

Which responsibilities will be yours?

  • Leading and taking decisions for the QA Team
  • Implement a quality vision within the global team of InoKura
  • Management of the quality system of InoKura and ensure its implementation:
    • Writing procedures and/or assisting colleagues in writing procedures
    • Review and approval of procedures
    • Maintaining the SOP revision schedule
  • Management of equipment qualification, installation and maintenance
  • Management and participation in sponsor audits and regulatory inspections
  • Management and participation in InoKura’s internal and external
  • Ensure that CAPA incidents and deviations are documented and ensure the follow-up of the CAPA plan in due time
  • Ensure corrective and preventive actions are implemented and documented
  • Management of quality records and documentation
  • Set up and management of training and formation plans and
  • Maintains compliance with federal, state, local, and organizational laws, regulations, guidelines, and policies
  • Proactively take part in the Quality System continuous improvement by conducting performance evaluations that are timely and constructive.
  • Regularly report the quality system status to the General Management based on the quality plan
  • Carrying out field work with the various teams to learn about the changes to be made

Does all of this speak to you? Let’s take a look at the qualifications required :

  • You have a Master degree as minimum preferably in life sciences.
  • You have knowledge in Quality Management and GDP knowledge is a plus.
  • Previous experience in clinical trials is a plus but not
  • You’re fluent in French and have a good level in English (B2 level is expected)
  • Excellent interpersonal and communication
  • Demonstrated leadership
  • Excellent organizational skills and attention to
  • Excellent time management skills with a proven ability to meet
  • Strong analytical and problem-solving skills
  • You master the use of IT
  • You are dynamic and You love to be challenged
  • You are flexible and quality

If you like everything, here’s what we have to offer :

  • A 4/5 time or full time job that values experience
  • A flexible time shift
  • Internal or consultancy contract
  • A dynamic environment with renown partners that are at the forefront of pharmaceutical excellence
  • A human sized company that will help you sharpen your skills and take initiatives

Do you share our expectations? What are you waiting for?

Please send your CV and cover letter to rh@inokura.be

rh@inokura.be

Les études cliniques en cours chez InoKura

Études cliniques en cours