Quality Engineer III

Overview

The R + D Quality Engineer III leads and enforces product development quality initiatives through identifying, investigating, planning, and conducting activities aimed at ensuring robust and quality design and manufacturability of medical devices.

Responsibilities

• Plans, leads, and manages quality deliverables on new product development (NPD) projects in accordance with regulatory standards ISO9001 : 2015, ISO13485 : 2016, ISO14971, FDA, CSA, and EU MDR regulations.
• Leads all risk management processes and creates risk management documentation for (NPD) projects.
• Creates, reviews, and approves documentation related to the engineering Product Realization Process (PRP). Documentation includes, but is not limited to, change requests, engineering orders, product and component test specifications and design records.
• Facilitates the design and process failure mode and effects analysis (FMEA) process.
• Leads site-based quality department initiatives as a subject matter expert (SME).
• Applies domain expertise to the application and advancement of engineering methods and tools. Leads the application of six sigma techniques and drives continuous process improvement.
• Collaborates with cross-functional teams to align decisions with business goals.
• Mentors engineer I & II teammates, focusing on technical skills, collaboration skills, and cultural competencies.
• Applies advanced tools and methods to solve complex problems. Tackles technical challenges and contributes to troubleshooting effort.

Secondary Duties

Education and / or Experience

Bachelor's degree in engineering or related field and 4+ years of relevant experience, or equivalent combination of both. Certifications preferred : Certified Quality Engineer (CQE), Six Sigma Black Belt (DMAIC, DMADV), and Certified Reliability Engineer (CRE).

Competency and / or Skill

Supervisory Responsibilities

About Us

Founded in 1915, Midmark Corporation is the only company transforming healthcare experiences through innovative design within the medical, dental and animal health environments. With more than 2,200 teammates worldwide, Midmark focuses on harmonizing space, technology and workflows, creating a better experience for caregivers and patients at the point of care. The Midmark headquarters and innovation hub are located in Versailles, Ohio, which is also home to the Midmark Experience Center, Design Center, Technology Center and our largest manufacturing facility. Midmark maintains eleven additional locations in the United States, including four innovation hubs, and has subsidiaries in India and Italy.

EO / AA Employer Minorities / Females / Protected Veterans / Disabled

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