Quality Inspector I
In this role, you have the opportunity to
Perform visual, dimensional, in-process, and final inspections as defined by SOP and Engineering Drawings. Utilize good technical and analytical skills, have a strong understanding of inspection techniques to assure quality standards are maintained. Be flexible to move between Quality Control and other areas to support QC activities and have the opportunity to work in a team environment to efficiently maintain a high level of quality standards, productivity, and meet our customer demands.
You are responsible for
- Utilize Inspection Standard Operating Procedures and Engineering Drawings to perform quality inspections on consumable products, subassemblies, and raw material.
- Complete AQL sampling or 100% inspection.
- Utilize various measuring equipment and collect data to determine component acceptance.
- Generate Nonconforming Reports to record and control nonconforming material.
- Review LHRs for Good Documentation Practices and admin errors.
- Complete Keystone Line Auditing and In-Process Teammate Audits in accordance with SOP.
- Interface with Engineering, Quality, and Production Teammates to communicate quality standards and address issues in a timely manner.
- Participate in quality audits, including FDA, BSI, etc.
- Locate failures and recognize set-up problems.
- Perform Final Audit of pre-sterile products and documentation.
- Perform Sterile Load Release to FGI, reviewing vendor provided data.
- Perform Verification of proper Sterile Load Configurations.
- Perform on-line operational tests and inspections to insure production quality standards are maintained as associated with Keystone QC testing.
- Assist or train other Teammates.
- Successfully work in and promote a team oriented
- Required to work in cleanroom environment while performing consumable product Inspections.
You are a part of
Our inspection team and will be flexible to move between In-Process Inspection and Final Inspection areas to support QC activities and the opportunity to work in a team environment to efficiently maintain quality standards and meet our customer demands.
To succeed in this role, you should have the following skills and experience
- High School diploma or equivalent
- Minimum 1+ years in Quality Control or Quality Assurance in electrical, mechanical, or aviation inspection or medical device manufacturing experience
- Experience with AQL Sampling using C=0 Sampling Plan
- Knowledge and use of precision testing equipment and tools
- Ability to lift and work with parts or sub-assemblies weighing up to 50lbs
- Computer abilities with web based systems
- Cleanroom Environment Experience (Preferred)
- Government Regulated Environment experience such as FDA or ISO (Preferred)
In return, we offer you
At Philips, we strive to make the world healthier and more sustainable through innovation, and our goal is to improve the lives of 3 billion people a year by 2025. This position offers the opportunity to impact worldwide regulatory compliance and directly improve the customer and patient experience.
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. Our people experience a variety of unexpected moments when their lives and careers come together in meaningful ways.
To find out more about what it’s like working for Philips at a personal level, visit the Working at Philips page on our career website, where you can read stories from our employee blog. Once there, you can also learn about our recruitment process, or find answers to some of the frequently asked questions.
It is the policy of Philips to provide equal employment and advancement opportunities to all colleagues and applicants for employment without regard to age, color, citizenship, disability or perceived disability, ethnicity, gender, gender identity or expression, genetic information, marital or domestic partner status, military or veteran status, national origin, pregnancy/childbirth, race, religion, sexual orientation, or any other category protected by federal, state and/or local laws. Philips is an equal employment opportunity and affirmative action employer Disability/Veteran.
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.
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