It’s a calling to create a healthier society through meaningful work, focused on improving 2.5 billion lives a year by delivering innovative solutions across the health continuum. We welcome you to a challenging, innovative environment with great opportunities for you to explore. Good in verbal and written communication skills in English, Dutch is a plus. Good organisational skills and able to take responsibility Quality-conscious, disciplined, accurate, honest and representative Knowledge and experience of quality management systems and regulatory affairs To succeed in this role, you should have the following skills and experienceĪ Bachelor’s (BSc) or Master’s (MSc) degree in electronic engineering Īt least 5 years of practical experience in the field of (Safety Compliance) Testing The QLAB is an independent laboratory and operates within its own Quality Management System. The QLAB plays a vital role in ensuring the patients’ safety by demonstrating compliance with the relevant safety standards. Support the Quality Manager on technical issues during audits Ī small, but dedicated team of Test Engineers. Is attentive for nonconforming work and reports this if applicable Set-up, test, maintain and troubleshoot test and measurement equipment, including software, for the purpose of testing and measuring assemblies and/or final systems and related items Operate test and measuring equipment analyze any potential failure in the measurement equipment keep a strict calibration regime Prepare and compile test reports according to internal requirements and international standards ĭevelops and adapts procedures and working instructions in accordance with the document control procedures, validates non-standard methods Independently plan and perform tests according to prescribed procedures Īnalyze and interpret test results balance observations with the test specification and international standards ĭecide on compliance (judge on pass/fail of each test against the performance criteria) Technical (with respect to safety compliance testing): Initiate changes, if applicable, for all instructions and templates relevant to the work of testing Provide feedback based upon the experiences gained and cooperate in corrective and preventive actions Give recommendations to continually improve the Management System of the QLAB You will interpret and report test results and report to the Manager Quality Laboratory. Limitations consist of (a) Identification of CME needs (b) Determination of educational objectives (c) Selection and presentation of content (d) Selection of all persons and organizations that will be in a position to control the content of the CME (e) Selection of educational methods (f) Evaluation of the activity.In this role, you have the opportunity toĮxecute objective and reproducible safety tests of the Quality Laboratory (QLAB). The AMA Standards for Commercial Support clearly prohibit any commercial interest from control of CME activities. The education programs provided by Philips are NOT eligible for AMA Category 1 CME credits through Philips. This activity may be available in multiple formats or from different sponsors. ARRT regulations state that an individual may not repeat a lecture presentation for credit if it was reported in the same biennium. However it is the responsibility of the REGISTRANT to assure the ASRT credits are acceptable for his or her purposes. Many of our courses are approved for CEU credit by the ASRT, which have been accepted by ARDMS and ICAEL, ICAVL. We have a wide variety of courses to accommodate your education needs, from core ultrasound courses to high level peer-to-peer courses.
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