profile

Laurent Collignon

System Engineer

Brussels, 1140, Belgium

Skills

Project Management

Prioritize workflow

About

- Four years of experience in clinical and medical research. Experience within the biotech industry including R&D environment. - Experience in supervising and managing projects. - Able to work within a small but quickly improving structure. - Strong interpersonal and communication skills. - Autonomous and proactive. I am open-minded, flexible and have a strong sense of service. - Abilities to organize and to prioritize workflow and to meet established time frames.

Education

ULB

Biomedical Engineering , Biomedical Engineering

June 2008 - June 2008

Experience

System Engineer

IBA , Louvain-La-Neuve

August 2010 - January 2012

Managing international and technical projects for Proton Therapy centers: - Lead and supervise in-house teams and international subcontractors to deliver products on time - Participate in the creation of the budget - Go on site to test and debug our product - Review and validate technical documents (requirements, test procedures,…) - Meet with customers to define the product they need - Demonstrate our products to new customers The goal is to develop and maintain a Patient Positioning Systems using any imaging technique such as fluoroscopy, CTs, MRIs and X-rays. It involves traveling abroad 30 % of the time.

Project Management
Technical specifications
Customer relationship
Software Engineer

Biomedical System , Brussels

August 2008 - August 2010

-Assist and lead the continued development and direction of the Imaging database, medical viewer and analysis applications. -Supervise international projects -Study Center Management and Client Communication. This includes: site qualification, site training and site support. -Meet with clients to develop the user requirements necessary for applications development in support of assigned projects. -Assist in discussions and presentations when necessary to support business development efforts. -Follow guidelines consistent with Good Clinical Practices and internal Standard Operating Procedures. -Write key documents for the set up of clinical trials -Create and assist in the validation documentation of the applications created. -Provide assistance in training clients and department personal on applications and systems use within the division and specific projects.

Programming: C++
Technical specifications
Customer relationship
Research Assistant (internship)

UCL , Louvain-La-Neuve

August 2007 - January 2008

-Python/Fortran/C++ programming to support and create custom application. -Validating CFD (Computational Fluid Dynamics) programs.

Python
C++
Fortran

Workplace personality

100+

Company Size

12

Day Length

25+

Team Size

Loud

Noise Level

Formal

Dress Code

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