Dr. Guy D. Foe Owono

 Act as Safety Officer pursuant to § 30 Medical Devices Act  Participate with other senior managers to establish strategic plans and objectives.  Develop quality standards for company products.  Interact with executive level and implement the company's policies, programs, and guidelines.  Provide process training for all employees including senior managers and executive level as required.

 Directed the activities of the V&V group and Reliability team involved in 24/7 operation.  Directed overall product testing, reliability testing and process quality continuous improvement initiatives realizing 25% increase in department efficiency and achieving ultimate objective of ONE defect call per month.  Organized and provided daily briefing to the General Manager of Philips Healthcare and her executive staff on progress made during V&V and reliability testing.

 Directed overall product testing, reliability testing and process quality continuous improvement initiatives realizing 25% increase in department efficiency and achieving ultimate objective of ONE defect call per month.

 Participated as a project team member in cross-functional project team activities.  Generated, maintained and implemented V&V documents for all products under my supervision.  Performed periodic bug scrub and communicated feedback to R&D staff regarding test findings.

 Conducted research on scattering problems in Nuclear Medicine and evaluated the use of a 3D fuzzy-segmentation method for volume quantification in Nuclear Medicine (SPECT, PET, MCD)  Evaluated the use of Transmission-Emission Computed Tomography for improved volume quantification using both dual and triple detector SPECT systems in SPECT  Provided trainings to Physician staffs on the effectiveness of various scatter & attenuation correction methods