Quality Engineer II

Posted 12 Days Ago
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Versailles, OH, USA
In-Office
Junior
Healthtech
The Role
Support and improve medical device quality through QMS maintenance, regulatory compliance (FDA/ISO/etc.), design control, FMEA, testing/validation, process improvements, cross-functional problem-solving, and mentoring junior engineers.
Summary Generated by Built In

JOB SUMMARY:

Identifies, investigates, plans, and conducts activities to improve or ensure quality through design and manufacturing of medical devices and components. Cross-functionally collaborates with R+D engineering, manufacturing, technical service, and supply chain to manage quality, compliance and cost of medical devices and components.


ESSENTIAL/PRIMARY DUTIES:

  • Ensures that products and product changes comply with all specified regulatory agencies (FDA, ISO, UL, CSA, etc.).
  • Assists in developing, maintaining, and improving the Quality Management System (QMS) to ensure compliance to all specified regulatory agencies.
  • Drives product quality improvements internally and externally by working with design, manufacturing, and supply chain.
  • Identifies testing and validation opportunities, contributes to product and process improvements.
  • Works on moderately complex projects, generates alternatives, and conducts testing.
  • Applies new tools and identifies opportunities for improvements using six sigma methods.
  • Conducts the design and process failure mode and effects analysis (FMEA) process.
  • Participates in Design Control Process (including design input, design output, reviews, qualifications, validations, etc.).
  • Identifies and communicates risks, participates in issue resolution, mentors junior engineers.
  • Applies advanced engineering methods and tools to solve engineering problems.

SECONDARY DUTIES:

  • Provides leadership, coaching, and/or mentoring to the co-op group and level I engineers.
  • Supports internal and external QMS audits and/or investigations.
  • Understands engineering documentation such as engineering drawings, bill of materials, change orders, testing documents and DHF/DMR records.
  • Follows industry standards and regulations for quality, safety, and performance.

EDUCATION and/or EXPERIENCE:

Bachelor's degree in engineering or related field and 2+ years of relevant experience, or similar combination of both. Six Sigma Greenbelt certification is preferred.


COMPETENCY and/or SKILL: 

  • Fully understand basic engineering tools and methods
  • Mastery of software programs - Microsoft Word, PowerPoint, Excel, Project, Minitab
  • Strong written and verbal communication skills
  • Ability to contribute ideas for process changes and improvements
  • Ability to define and analyze complex problems
  • Ability to generate alternatives and take reasonable risks to solve technical problems

 

SUPERVISORY RESPONSIBILITIES:

  • Provides leadership, coaching, and/or mentoring to level I engineers and co-op's.
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




Skills Required

  • Bachelor's degree in engineering or related field
  • 2+ years of relevant quality/engineering experience
  • Knowledge of FDA, ISO, UL, CSA regulatory requirements
  • Experience with Quality Management Systems (QMS) and Design Control
  • Experience conducting FMEA (design and process)
  • Mastery of Microsoft Word, PowerPoint, Excel, Project, and Minitab
  • Experience with testing, validation, and process improvement methods
  • Strong written and verbal communication skills
  • Ability to read and understand engineering drawings, BOMs, DHF/DMR records
  • Six Sigma Greenbelt certification
  • Experience mentoring or coaching junior engineers/co-ops
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The Company
HQ: Versailles, OH
1,281 Employees
Year Founded: 1915

What We Do

Midmark Corporation is the only clinical environmental design company that enables a better care experience for the medical, dental and animal health markets. With nearly 2,000 teammates worldwide, Midmark focuses on harmonizing space, technology and workflows, creating a better experience for caregivers and patients at the point of care. Visit midmark.com/careers for information on current career opportunities.

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