Philips Quality Engineer III in Ontario, California

• Provide quality engineering leadership in support of manufacturing process validation and new product transfer to production.

• Active participation with Operations, Product Development, Engineering, Purchasing, Production and Regulatory/Quality Assurance teams for quality engineering projects.

• Participate in life cycle management cross-functional teams to qualify changes or new processes.

• Maintain and monitor master validation plan to lead validation or qualification tasks for the equipments or processes.

• Develop inspection and test plans, test methods, work instructions and procedures for improvements and compliance.

• Participate in lean manufacturing or improvement projects.

• Review and approve product and process change control documentation (ECN).

• Develop, review or approve process and equipment validations/qualifications (IQ, OQ and PQ).

• Develop and communicate quality engineering or project reports to the management and cross-functional teams.

• Work with multiple departments to perform product or process failure investigation and root cause analysis. Recognize problems and recommend solutions to resolve the problems.

• Participate in internal and external (suppliers) audits.

In this role, you have the opportunity to

POHC (Philips Oral Healthcare Ontario) will be a world-class manufacturing and distribution site for H&W by utilizing our unique expertise to deliver meaningful and innovative healthcare products to customers worldwide. We will be a place where people, who share our passion, want to work.

You are responsible for

  • Ensures that appropriate validations and quality plans are developed and implemented for new products, new processes and for ongoing manufacturing.

  • Monitor processes: trend analysis, assess impact and follow-up to drive improvements.

  • Perform process audits and internal audits for regulated products to assess the effectiveness of the QMS linked to production controls.

  • Review change notices and assess which processes need validation/re-validation after changes, and verify processes and plans/records.

  • Participate in cross-functional project teams to deliver IQ/OQ and PPQ per project timeline.

  • Manage specific quality and compliance projects as needed.

  • Learn and practice Philips Excellence tools and implement lean program in quality engineering processes.

  • Provide quality engineering leadership in support of manufacturing process validation and new product transfer to production.

  • Active participation withOperations, Product Development, Engineering, Purchasing, Production and Regulatory/Quality Assurance teams for quality engineering projects.

  • Participate in life cycle management cross-functional teams to qualify changes or new processes.

  • Maintain and monitor master validation plan to lead validation or qualification tasks for the equipment or processes.

  • Develop inspection and test plans, test methods, work instructions and procedures for improvements and compliance.

  • Participate in lean manufacturing or improvement projects.

  • Review and approve product and process change control documentation (ECN).

  • Develop, review or approve process and equipment validations/qualifications (IQ, OQ and PQ).

  • Develop and communicate quality engineering or project reports to the management and cross-functional teams.

  • Work with multiple departments to perform product or process failure investigation and root cause analysis. Recognize problems and recommend solutions to resolve the problems.

  • Participate in internal and external (suppliers) audits.

You are a part of

At POHC Ontario, we improve lives worldwide through state of the art manufacturing and distribution of innovative healthcare products.

To succeed in this role, you should have the following skills and experience

  • Bachelor’s degree or Master’s degree

  • 5 years of quality engineering exp.

  • Prefer medical device knowledge (FDA)

  • Experience with IQ,QQ,PQ

In return, we offer you

The ability to work in a fast moving consumer good medical space with like minded individuals.

Why should you join Philips?

Working at Philips is more than a job. It’s a calling to create a healthier society through meaningful work, focused on improving 3 billion lives a year by delivering innovative solutions across the health continuum at http://www.philips.com/b-dam/corporate/corporateblog/2016/PhilipsChronicDisease_5.jpg . Our people experience a variety of unexpected moments when their lives and careers come together in meaningful ways. Learn more by watching this video .

To find out more about what it’s like working for Philips at a personal level, visit the Working at Philips page at http://www.philips.com/a-w/careers/healthtech/working-at-philips/working-at-philips.html on our career website, where you can read stories from our employee blog at http://www.usa.philips.com/a-w/our-people/life-at-philips.html . Once there, you can also learn about our recruitment process at http://www.philips.com/a-w/careers/healthtech.html , or find answers to some of the frequently asked questions at http://www.philips.com/a-w/careers/healthtech/faq.html .

Philips is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex (including pregnancy), sexual orientation, gender identity, national origin, genetic information, creed, citizenship, disability, protected veteran or marital status.

As an equal opportunity employer, Philips is committed to a diverse workforce. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants that require accommodation in the job application process may contact 888-367-7223, option 5, for assistance.