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Working at Freudenberg: "We will wow your world!" This is our promise. As a global technology group, we not only make the world cleaner, healthier and more comfortable, but also offer our 51,000 employees a networked and diverse environment where everyone can thrive individually. Be surprised and experience your own wow moments.

At Freudenberg Medical, we make products that save and improve the lives of people every day, all around the world. We are a global provider for medical device design and manufacturing with more than 2,500 employees. Innovation is at the core of our company, and we are proud of our industry-leading quality, lean manufacturing, and focus on innovation in products and processing technologies. Freudenberg Medical is an exciting place to work with lots of opportunity to learn, develop, and grow your career. Come join us and together we can make a difference in the future of healthcare.

Some of your Benefitsarrow_right

401K Match

401K Match

401K Match
401K Match: Save for retirement with the company's help.
Diversity & Inclusion

Diversity & Inclusion

Diversity & Inclusion
Diversity & Inclusion: We focus on providing an inclusive environment and recognize our diversity contributes to our success.
Personal Development

Personal Development

Personal Development
Personal Development: We offer a variety of trainings to ensure you can develop in your career.
Sustainability & Social Commitment

Sustainability & Social Commitment

Sustainability & Social Commitment
Sustainability & Social Commitment: We support social and sustainable projects and encourage employee involvement.
Corporate Events

Corporate Events

Corporate Events
Corporate Events: We celebrate success as a team, because only together can we achieve our goals.
Pay Range: $70K to $85K, depending on experience
NO Visa sponsorship
location_on Baldwin Park, CA
WorkplaceOn-Site
trip_origin Freudenberg Medical LLC
You support our team as

Quality Engineer I

Responsibilitiesarrow_right

  • Performs all measures of quality planning for incoming and in-process inspections as well as final acceptance – Develop and support the generation of Flow charts, FMEAs and Control plans
  • Supports plant activities in process validation, process capability issues and customer issues, initiates corrective and preventive action, with an eye to increased capability, reduced inspection time/effort, customer satisfaction and supports Quality System implementation.
  • Transition products from development to manufacturing by composing and/or reviewing protocols and reports for the IQ/OQ/PQ process
  • Establish statistical standards of performance by providing support and expertise in Gage R&R, DOE, reliability strategy, and analytical problem-solving techniques.
  • Assures compliance to in-house and external specifications and standards, such as GMPs, GDPs, ANSI and ISO regulations.
  • Performs/leads with the investigation of root cause and determination of corrective and preventive actions relating to NCMRs and CAPAs Interfaces with manufacturing and engineering to resolve quality issues for new and existing product lines.
  • Works on continuous improvement projects from beginning to end. Characterizes the problem, identifies key process inputs, determines optimal operating window, implements controls to maintain output at desired level and quantifies the improvement in savings, avoidance, or value.

Qualificationsarrow_right

  • Bachelor of Science degree in Engineering or equivalent
  • 2 - years of experience as a Quality Engineer or quality focused internship
  • 2 + years of experience in a manufacturing environment of medical or health care products and knowledge of injection molding processes
  • Understanding or experience in performing and executing Gage R&R studies using Minitab
  • Demonstrated knowledge in Quality System Requirements/Good Manufacturing Practices.
  • Proficient with reading engineering drawings, written specifications, production documentation, using calibrated inspection equipment such as gauges, calipers, smart scope, multi-meters, manometers, pull test and other inspection equipment.
  • Proficiency in the use of PC and programs, particularly Excel and Word to create procedures, work instructions, forms etc., along with working knowledge of SolidWorks and AutoCAD software, 2D& 3D, Microsoft Project, and SAP
  • Understanding of continuous improvement methodologies including Lean/Six Sigma and validation.
  • Detail orientation; strong organizational skills and bias for action.
  • Strong team oriented professional with good interpersonal skills who is hands-on with a high energy approach to work
  • Ability to communicate ideas and information clearly, effectively, and frequently (oral and written).
  • Execute tasks in a timely manner without direct supervision.
  • Ability to travel as required (minimal).
  • Preferred Qualifications
  • Certified Quality Engineer (CQE) and or Certified Quality Auditor (CQA).
  • Lean/Six Sigma certification.
  • Injection molding manufacturing.
The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.

Additional Informationarrow_right

RecruiterRachel Peterson
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