**PLEASE NOTE** ACTUAL JOB TITLE** CAPA FACILITATOR**
**Position is remote anywhere in the US**
**Max Bill Rate $65, Superior Candidates Max Bill Rate $75

CAPA Facilitator

Job Description
Philips is a global leader in health technology, committed to improving billions of lives worldwide and striving to make the world healthier and more sustainable through innovation. Driven by the vision of a better tomorrow.
But it s not just what we do, it s who we are. We are 80,000, wonderfully unique individuals, with two things in common. An unwavering sense of purpose and a relentless determination to deliver on our customers needs. It s what inspires us to create meaningful solutions the kind that make a real difference when it matters most.
The world and our customers needs are changing faster than ever before and while we are proud of what we do already, we know we can do more. That s why we need you, to help us tackle increasingly complex challenges posed by ever evolving health and well-being needs.

In this role, you have the opportunity to make life better
Looking at the challenges the world is facing today Philips purpose has never been more relevant. So whatever your role, if you share our passion for helping others, you ll be working towards creating a better and fairer future for all.
You will support the Corrective and Preventive Action (CAPA) process from issue identification to closure and ensuring adequate execution of process and the quality of CAPA record content.

You are responsible for
Supporting CAPA activities: assessing complex investigations and corrective actions, reviewing test and other complex performance data, leading complex root cause analysis and quality problem solving
Facilitate product and process CAPA investigations from issue identification through implementation of solution and effectiveness monitoring
Support CAPA Owner in all aspects of CAPA activity which includes gaining the commitment of cross functional resources, scheduling CAPA team meetings, and ensuring CAPA deliverables per project timelines
Support CAPA Owners in the presentation of CAPAs during audits and CAPA Review Board meetings
Mentor cross functional teams with the implementation of appropriate root cause analysis techniques
Mentor the analyze of quality monitoring data sources and apply statistical techniques to identify existing and potential causes of non-conformances

You are a part of
Our Quality & Regulatory organization, supporting Image Guided Therapy Systems.

To succeed in this role, you ll need a customer-first attitude and the following
B.Sc in Engineering or other relevant academic field as statistics, quality management, etc., advanced degrees an advantage
5+ years experience in quality roles in medical device or other regulated industry
Working knowledge of appropriate global regulations, requirements, and standards such as 21 CFR Parts 803, 806, and 820, ISO 13485, and ISO 9001, and ISO 14971
Good understanding of statistical methods, quality tools, problem solving tools and methodologies (i.e. 8D, DMAIC, SPC, FMEA, Control Plan, LEAN) an advantage
Experience as team facilitator / team coach
Work experience in complex organizations with Manufacturing, R&D and Engineering environments
Strong communication and interpersonal skills, ability to coach teams in matrix environment cross-functional teams
Ability to resolve complex issues in creative ways and influence stakeholders accordingly
Multi-tasking and decision-making capabilities
Self-starter, motivated, action-oriented
Experience working in global corporate environment
Fluent English