Hi All!
We are seeking a several Quality Investigations Specialists to join our Nuclear Medicine team here at Philips.
Pick your location. You can be based in San Jose, CA or Cleveland, OH or Fitchburg, WI.
I have included the job description below but feel free to send a resume and we can talk over the details further.
Have a great day!
Katie
katie.mcauliffe@philips.com
Quality Investigations Specialist
Candidate Responsibilities
1. Responsible to take assigned investigations from evaluation to closure in accordance with internal and external (FDA, Canadian and European) regulatory requirements.
2. Identify product complaints per regulatory definition.
3. Responsible for getting the basic facts related to a reported issue and follow up if necessary.
4. Complete investigations in a timely manner.
5. Present data in a clear and concise manner in accordance with Standard Operating Procedures into the complaint record.
6. Identify potential safety problems.
7.Provide manager all identified potential safety problems under investigation including aware date of the complaint to ensure timely submission of problem reports to government agencies, if required.
8. Prepare Safety Committee Presentations.
9. Investigate complex clinical and technical issues.
10. Utilizing nuclear medicine product knowledge, reproduce a reported problem and if necessary get the appropriate product specialist or Engineer involved to resolve the problem or provide root cause.
11. Research company documentation to reference in the complaint record and/or safety committee presentations.
12. Trend and Issue Report Generation
13. Travel 10- 15%.
Katie McAuliffe
Recruitment Sourcing Specialist
Philips
3000 Minuteman Road
Andover, MA
978-659-7542
katie.mcauliffe@philips.com
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