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Supplier Quality Auditor in Virtual, North Carolina at Stryker Corporation

Date Posted: 4/13/2019

Job Snapshot

Job Description

Lead supplier evaluations in the Global Supplier Quality Audit program to support the evaluation, selection, approval, and monitoring of suppliers and manufacturing partners.  The role is responsible for the coordination and implementation of on-site and documentation audits, related observations, NCs, CAPAs and communication of evaluation results to key stakeholders.  Provide cross-functional supplier auditing services to Stryker’s R&D, Acquisition, Manufacturing, Materials, Purchasing, and Operations stakeholders worldwide.     The top three performance objectives for this role are: (1) drive continuous improvement within the Stryker supply base, (2) ensure compliance and conformance, and (3) ensure effective and efficient Quality Management Systems are established, documented, implemented, and maintained.   

Who we want

Analytical problem solvers. People who go beyond just fixing to identify root causes, evaluate optimal solutions, and recommend comprehensive upgrades to prevent future issues.

Dedicated achievers. Relentless about quality, people who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.

Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, information, use cases, and industry analyses to develop best practices.

What will you do

Complete risk-based audits of suppliers per Stryker’s required cycle times to ensure conformance and compliance.

Provide compliant records for FDA, ISO, Corporate, Internal, 2nd party, and Operations audits.

Ensure supplier Quality Management Systems comply with applicable FDA and ISO regulations and requirements.

Identify and write findings during evaluations and drive timely closure of NCs through the CAPA system.

Ensure components, sub-assemblies, and devices meet all print specifications and applicable regulations.

Who we want

1-2 years of relevant experience in Quality, Management, or Engineering

Bachelor of Science in engineering, or engineering related discipline required

Experience in medical device industry preferred

Experience working onsite developing suppliers preferred

Experience conducting supplier audits and internal audits preferred

Work From Home: Yes

Travel Percentage: Up to 75%

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.

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