Senior Quality Inspector

Stryker · Plainfield, United States · full time · On site · 6 days ago

Sign up to apply
Your first one is free
Posted October 07, 2026 · Read from Stryker
Why a CV for this job?

94% of employers say their filters drop qualified candidates whose CV does not match the ad's exact criteria (Harvard Business School, 2021).

  • They see what they asked for, first. Your experience that matches the ad leads, in the ad's own words, so someone skimming finds it in seconds.
  • It gets past the software. Many larger employers use software that ranks CVs by how closely they match the ad, often before anyone reads them.
  • In the language of the ad. An ad written in Spanish gets a CV in Spanish, even when yours is in Portuguese.
  • Your facts, nothing invented. Your own experience, reordered and reworded. What the ad wants and your CV does not show is listed for you to add, only if it is true. You check it before you send it.
See an example

Work Flexibility: Onsite

Position Summary

The Senior Quality Inspector role sits within Stryker's US Central Distribution Center, supporting reverse logistics. This individual contributor role is responsible for inspecting and dispositioning product returns coming through the center.

Why Join Stryker?

Stryker is one of the world's leading medical technology companies and is consistently ranked as one of the best places to work globally. Our total rewards package includes bonuses, healthcare, insurance benefits, retirement programmes, wellness programmes, and service and performance awards.

What You'll Do

  • Perform formal review of product packaging and associated labelling to ensure they meet company and regulatory standards.
  • Work from engineering drawings, prints and associated guidance documents to perform accurate checks and assessments of finished goods.
  • Follow and explain detailed instructions and job-related procedures, including regulatory procedures and policies.
  • Use electronic data entry systems and associated ERP platforms accurately and efficiently.
  • Prioritise work effectively and efficiently across competing demands.
  • Apply understanding and knowledge of Quality discipline procedures and concepts to daily tasks.

What You'll Need

  • 1+ years in medical device or other regulated industry experience preferred.
  • Prior experience with quality control and/or inspection.
  • ERP systems experience (SAP) preferred.
  • This is an individual contributor role requiring the use of professional judgement, with an expectation to work independently with minimal supervision.
  • Strong interpersonal skills, both written and verbal.

$26.60

Travel Percentage: 10%

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.

Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.

Employer
Stryker
Location
Plainfield, United States · On site
Contract
full time