招聘人数:1-2人
到岗时间:不限
年龄要求:不限
婚况要求:婚姻状况
In this role, you have the opportunity to
As the incumbent of this Quality & Regulatory (Q&R) role within Philips, your challenge will be to guide and support Business Groups, Markets and enabling functions to always do the right thing. This involves being a confident advisor on approval, regulatory compliance and quality management related topics, in order to achieve timely releases of innovative products that deliver high quality and outstanding reliability to the lives they will improve.
You are responsible for
Working in the medical industry brings much fulfillment, as well as unique challenges. As part of our HealthTech focused company, you will be responsible for successfully dealing with and managing Philips relationships with approval agencies such as the US Federal Drug Administration (FDA).
· Manage activities within the CAPA process. Manage workflow in the CAPA process.
· Support the CAPA process by facilitating CAPA training.
· Demonstrate effectiveness in task completion, decision-making, empowerment of others, exception management, training, problem solving and team leadership. Lead CAPA activities, and provide assistance in other Quality areas, as needed
· Maintain a high level of expertise in current regulatory root cause investigation requirements, and serve as a resource for compliance to these requirements
· Recognized as a CAPA expert
· Lead CAPA process improvement initiatives and implement according to scheduled timelines
· Participate and support internal and external inspections and assist with implementing solutions to audit findings
· Perform periodic trend analysis and corrective action effectiveness measures of all quality system events and identify opportunities for improvement.
· Facilitate weekly Corrective Board meetings
You are a part of
As a result of Philips renewed commitment to Quality, it has recently restructured its organization to ensure you and your department have clear interfaces with Philips Business Group and Market leadership, and can harness the expertise of five Centers of Excellence (COEs). These 5 COEs specialize in the following capabilities: Regulatory & Clinical Affairs, Supplier Quality, Quality Management System, Quality Assurance & Engineering, and Compliance & Audit. As part of this new structure, you are empowered to use your voice and expertise to have a positive impact on your team, our business, and health technologies that will improve the health, well-being and care for people around world.
To succeed in this role, you should have the following skills and experience
A person who is excited by the unique professional challenges that our Quality Transformation presents, has strong technical competencies, and demonstrates resilience challenging, often demanding situations. We are looking for a perfectionist- a fixer who continuously strives for excellence as a way of life; not just as a job. We’re looking for someone who can inspire others to adopt this mentality of prioritizing quality above all else in a relentless pursuit to improve the quality of life billions for the billions of people Philips brand touches each year.
· 3-5 years+ with CAPA
· Excellent communication skills
· Ability to resolve conflict, influence leaders
· Strong verbal and written communication skills.
· cross-functional team experience
· Drive and implement process improvement
· FDA, ISO and Quality systems is also required.
· Must be bilingual
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