Philips Quality Manufacturing Engineer 

United States, Pennsylvania 

572180563

In this role you will be responsible for:

• Supports creation and maintenance of integrated supply chain related quality plans including all stages of the life cycle of the product within the manufacturing and distribution processes.

• Performs independent technical assessment on non-conforming materials including adverse effect assessments as they relate to the manufacturing and distribution processes.

• Can lead quality related problem solving and root cause analysis during the manufacturing and distribution processes.

• Uses analytics and statistics to report on product quality key performance indicators and related quality management system quality metrics. Provides feedback to operations, supplier quality and/or product industrialization engineering teams.

• Frequently interacts with functional peer groups. Success cross-functional interaction requires the ability to gain cooperation of others while conducting presentations of technical information concerning specific projects or schedules.

• Follows processes and operational policies in selecting methods and techniques for obtaining solutions.

• Work on issues of diverse scope where analysis of situation or data requires evaluation of a variety of factors, including an understanding of current business trends.

You're the right fit if:

• A Bachelor’s degree in engineering or science or equivalent experience in the medical device industry

• 3+ years of related experience.

• Working knowledge of appropriate global regulations, requirements, and standards.

• ASQ certified Quality Engineer preferred.

• Have an understanding of quality philosophies, principles, systems, methods, tools, standards, organizational and team dynamics, customer expectations and satisfaction, supplier relations and performance, leadership, training, interpersonal relationships, improvement systems, and professional ethics.

• Have understanding of a quality system and its development, documentation, and implementation with respect to domestic and international standards or requirements.

• Be able to support the development and implementation of quality programs, including tracking, analyzing, reporting, and problem solving.

• Have an understanding of the audit process including types of audits, planning, preparation, execution, reporting results, and follow-up.

• Be able to support product and process quality in accordance with documented procedures and external statutory and regulatory requirements (which includes, but is not limited to: planning processes, material control, acceptance sampling, and measurement systems).

• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this .

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

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If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion .

US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.

Company relocation benefits will not be provided for this position. For this position, you will reside in or within commuting distance to Murrysville, PA. USA