- Implementing the Computer System Validation process and writing of the corresponding SOPs- Training of the collaborators- Coordinating the validation of the Computer Systems of the company

- Implementing GDPR related SOPs- Training IPG/BIO.be collaborators - Review of Data Protection Agreements- Performing DPIAs, management of the record of processing activities, management of the subjects requests...- Link with the Data Protection Authorities

- Reorganization of the Immunochemistry laboratory (review of the processes, materiel and equipement management, SOPs....) - Project management : management of specific projects between IPG/BIO.be and clients (from work order, to implementing of the processes, reporting and follow-up)

1. Provide support for Global Regulatory Affairs Risk Management• Help in the process of periodic review of the RU and RR • Work /communicate with the other Compliance Units, other departments impacting GRA or other QRMs as appropriate2. Participate in audit/inspection management activities• Facilitate central process audit/inspection coordination in audit/inspection scoping, preparation, coordination and internal communication• Prepare/support the business for… Show more 1. Provide support for Global Regulatory Affairs Risk Management• Help in the process of periodic review of the RU and RR • Work /communicate with the other Compliance Units, other departments impacting GRA or other QRMs as appropriate2. Participate in audit/inspection management activities• Facilitate central process audit/inspection coordination in audit/inspection scoping, preparation, coordination and internal communication• Prepare/support the business for audits/inspections (preparation meetings, advise during audit or inspection and on audit/inspection report responses)• Collaborate in follow up and tracking of corrective and preventive action plans (CAPAs) 3. Help in the management of L1 and L2 activities• Identify L1 monitoring activities that might exist within GRA• Participate in the creation of agreed QC forms, checklists or tabs to support L1 activities4. Providing advice and guidance on applicable policies and procedures to GRA customers• Provide consultancy in line with specific projects that are running or RA SOP review cycle needs• Work with Training & SOP Team as appropriate Show less

Working as a scientist at MDxHealth SA in Liège. This international company is developing real time MSP tests for detection and treatment improvements for different types of cancer. MDxHealth has an ISO Certified Service lab in Liege and intends to offer its products in North-America through a CLIA Certified Service Lab.My job implied planning, prioritizing and setting experiments according to ISO certification and internal design controls in the context of MDx Prostate cancer confirm… Show more Working as a scientist at MDxHealth SA in Liège. This international company is developing real time MSP tests for detection and treatment improvements for different types of cancer. MDxHealth has an ISO Certified Service lab in Liege and intends to offer its products in North-America through a CLIA Certified Service Lab.My job implied planning, prioritizing and setting experiments according to ISO certification and internal design controls in the context of MDx Prostate cancer confirm test. I was also part of the service testing department ruled by a Quality Management System. As the biosecurity officer, I was also in charge of implementing security procedures for L1 and L2 laboratories, providing training to employees and dealing with paper work related to European, Belgian and Walloon regulations. Show less

During five years I worked as project leader for lung and cervical cancers projects. I had to organize and plan the work in Oncomethylome facilities in Liège. The job also consisted in setting up procedures for collecting/conservation of different types of samples (tissue, blood and sputum), putting new techniques in place and resolving problems linked to all part of these projects, collecting clinical data, transferring of technologies to laboratories located in Holland, Belgium and… Show more During five years I worked as project leader for lung and cervical cancers projects. I had to organize and plan the work in Oncomethylome facilities in Liège. The job also consisted in setting up procedures for collecting/conservation of different types of samples (tissue, blood and sputum), putting new techniques in place and resolving problems linked to all part of these projects, collecting clinical data, transferring of technologies to laboratories located in Holland, Belgium and USA. I also had to analyze, synthesize and communicate results internally but also to external collaborators. Show less

My work consisted in visiting and providing information to physicians and specialists about drugs against osteoporosis.

During four years, I worked, together with a team of bio-engineers, in characterizing Rhizomania, a viral disease affecting sugar beet crops, in Belgium. Biomolecular tools such as PCR, real-time PCR ( I-Cycler / probes and SYBR-green), sequencing, bio-informatic analysis, cell culture, cloning, RFLP, production of viral particles, in-vitro mutagenesis ELISA and RT-PCR were used to carry out this work.This job also consisted in communicating results to RW (reports and oral… Show more During four years, I worked, together with a team of bio-engineers, in characterizing Rhizomania, a viral disease affecting sugar beet crops, in Belgium. Biomolecular tools such as PCR, real-time PCR ( I-Cycler / probes and SYBR-green), sequencing, bio-informatic analysis, cell culture, cloning, RFLP, production of viral particles, in-vitro mutagenesis ELISA and RT-PCR were used to carry out this work.This job also consisted in communicating results to RW (reports and oral presentations), in submitting scientific papers and participating to international congress.I also had the opportunity to supervise several students during their master thesis. Show less

Selling airline tickets, check-in, weight and balance and gate service.