CMM Programmer (Customs Quality Manufacturing Technician) - 23421BR - EN in Mahwah, NJ at Stryker Corporation

Date Posted: 3/11/2018

Job Snapshot

Job Description

Every day, our employees bring a passion to offer high quality medtech products and services that improve the lives of people around the world. That passion is the DNA of our company. We sum it up in the 11 words of our mission: “Together with our customers, we are driven to make healthcare better.” Our mission is at the heart of everything we do.

Taking great pride in developing and engaging our employees, Stryker was named to Fortune’s “Top 100 Companies to Work For” for and a Gallup Great Workplace in 2017. We are currently seeking a CMM Programmer for our Custom Products team in Mahwah, NJ.

Specific responsibilities of the CMM Programmer include, but are not limited to the following:
  • Perform dimensional and visual inspection to blueprint and guide sheets using standard gages, customized gages and comparators
  • Perform Document Review and Product Verification Inspection (PVI) in compliance to GMP requirements
  • Perform material and component Receiving Inspections
  • Inspect, calibrate and qualify gages
  • Perform Gage R&R support
  • Perform programming and operation of CMM, serve as lead CMM programmer
  • Maintain Clean-line maintenance and support for Specialty Instruments
  • Validation support on all equipment in cell
  • Verify First Article Inspection (FAI) data
  • Perform Oracle system transactions related to product inspections and release
  • Support supplier/vendor investigations related to Quality issues

Job Requirements

A minimum of a High School Diploma is required; relevant vocational or trade school training and/or apprenticeship program is highly preferred. A minimum of 5 years of product inspection experience in a GMP manufacturing environment is also required.

Ideal candidates will also possess the following skills/experience:
  • Experience with inspection of hand finishing, buffing, laser-marking, masking or blasting processes for Customized Implants and Specialty Instruments is preferred
  • Demonstrated ability to read and interpret implications on complex blueprints
  • Demonstrated CMM and/or OGP operation and CMM programming experience and proficiency
  • Demonstrated proficiency in the use of all standard inspection tools including calipers, micrometers, height gages, comparators and vision systems
  • Demonstrated ability to provide guidance for all aspects of Inspection and Receiving and provide review and generate Inspection Guide Sheets for new products
  • Demonstrated proficiency in Geometric Dimensioning and Tolerancing (GD&T)
  • Prefer demonstrated understanding of packaging or clean line process for instruments
  • Understanding of FDA CFR 820 and EN 13485 Regulations is preferred
  • Demonstrated communication and interpersonal skills, with the ability to work successfully in a team-based environment that heavily emphasizes quality, performance, cross training, customer service, and accountability
  • Experience collaborating with engineering teams and providing feedback and making recommendations to help achieve team goals in quality, cost and delivery
  • Self-motivated and driven, demonstrating the ability to manage and deliver projects while adhering to strict timelines
  • Demonstrated analytical and problem-solving skills including continuous improvement and lean methodologies
  • Proficient in Microsoft Excel, Access, Word and Outlook; proficient with Oracle requisitions
  • Ability to work weekday and weekend overtime hours as required to meet the demands of the team/business

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