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Internship Quality Engineer Medical Device Jobs in Ohio

Norman Noble Inc

Quality Engineer

Cleveland, OH · On-site

$69.80K - $90.20K/yr

Our state-of-the-art facilities support innovative solutions where we manufacture, finish and inspect medical device implants for customers worldwide. The Quality Engineer works with internal teams ...

Norman Noble Inc

Quality Engineer

Cleveland, OH · On-site

$69.80K - $90.20K/yr

Our state-of-the-art facilities support innovative solutions where we manufacture, finish and inspect medical device implants for customers worldwide. The Quality Engineer works with internal teams ...

Norman Noble Inc

Quality Engineer

Cleveland, OH · On-site

$69.80K - $90.20K/yr

Our state-of-the-art facilities support innovative solutions where we manufacture, finish and inspect medical device implants for customers worldwide. The Quality Engineer works with internal teams ...

Midmark

R+D Quality Engineer III

Versailles, OH

$66.70K - $86.10K/yr

JOB SUMMARY: The R + D Quality Engineer III leads and enforces product development quality ... Experience in the medical device industry and understanding of medical device quality systems and ...

Norman Noble, Inc.

Quality Engineer

Cleveland, OH · On-site

$69.80K - $90.20K/yr

Our state-of-the-art facilities support innovative solutions where we manufacture, finish and inspect medical device implants for customers worldwide. The Quality Engineer works with internal teams ...

Midmark Corporation

R+D Quality Engineer III

Versailles, OH · On-site

$66.70K - $86.10K/yr

JOB SUMMARY: The R + D Quality Engineer III leads and enforces product development quality ... Experience in the medical device industry and understanding of medical device quality systems and ...

Applied Medical Technology

Quality Engineer

Brecksville, OH · On-site

$68.40K - $88.30K/yr

Quality Engineer Department: Engineering Director of Regulatory Affairs Exempt Supervise the work ... Knowledge of commonly used concepts, practices, and procedures related to medical device ...

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Internship Quality Engineer Medical Device information

What are the key skills and qualifications needed to thrive as an Internship Quality Engineer in Medical Devices, and why are they important?

To thrive as an Internship Quality Engineer in Medical Devices, you need a basic understanding of quality assurance principles, regulatory standards (such as ISO 13485 or FDA regulations), and coursework in biomedical, mechanical, or related engineering fields. Familiarity with quality management systems (QMS), data analysis tools, and document control software is typically required. Strong attention to detail, analytical thinking, and effective communication help interns excel in identifying and addressing quality issues. These skills are crucial for ensuring product safety, regulatory compliance, and maintaining high standards in the medical device industry.

What types of projects and responsibilities can an Internship Quality Engineer expect in the medical device industry?

As an Internship Quality Engineer in the medical device field, you can expect to work on projects related to product inspections, documentation review, and process validation. You may assist in investigating non-conformances, supporting root cause analysis, and helping with risk assessments under the guidance of senior engineers. Interns often collaborate with cross-functional teams, including manufacturing, R&D, and regulatory affairs, to ensure products meet strict quality and compliance standards. This hands-on experience provides valuable insight into industry regulations and quality management systems, setting a strong foundation for future roles.

What does an Internship Quality Engineer do in the medical device industry?

An Internship Quality Engineer in the medical device industry assists in ensuring that products meet regulatory standards and company quality requirements. Their responsibilities typically include participating in product testing, documenting results, supporting root cause analysis for defects, and helping to improve manufacturing processes. Interns may also assist in reviewing quality documentation, conducting audits, and working with cross-functional teams to maintain compliance with standards like ISO 13485 and FDA regulations. This role provides valuable hands-on experience in quality assurance and regulatory affairs within the medical device sector.

What is the difference between Internship Quality Engineer Medical Device vs Quality Engineer Medical Device?

AspectInternship Quality Engineer Medical DeviceQuality Engineer Medical Device
QualificationsEnrolled in or recent graduate of relevant engineering or life sciences programBachelor's degree or higher in engineering, life sciences, or related field; certifications like CQE are common
Work EnvironmentInternship setting, supervised, entry-level tasksFull-time professional role, responsible for quality processes and compliance
ResponsibilitiesAssisting in quality audits, documentation, and process improvementLeading quality assurance activities, audits, and process optimization

The Internship Quality Engineer Medical Device role is an entry-level position designed for students or recent graduates gaining industry experience. In contrast, the Quality Engineer Medical Device is a full-time professional role with greater responsibilities in maintaining quality standards, compliance, and process improvements within the medical device industry.

What are the most commonly searched types of Quality Engineer Medical Device jobs in Ohio? The most popular types of Quality Engineer Medical Device jobs in Ohio are:
What cities in Ohio are hiring for Internship Quality Engineer Medical Device jobs? Cities in Ohio with the most Internship Quality Engineer Medical Device job openings:
Internship Quality Engineer Medical Device jobs near you
New Product Development Quality Engineer

New Product Development Quality Engineer

Norwood Medical

Dayton, OH • On-site

$69.90K - $90.30K/yr

Full-time

Posted 13 days ago

Norwood Medical rating

6.8

Company rating: 6.8 out of 10

Based on 21 frontline employees who took The Breakroom Quiz

Job description

Description
Norwood Medical is a premier manufacturer of high-precision medical components, specializing in advanced CNC machining for life-saving technologies. As we continue to expand our innovation pipeline, we are seeking a detail-oriented Quality Engineer to join our New Product Development (NPD) Team.
This is a critical role where engineering meets compliance. You will serve as the quality lead for new product launches, ensuring that every machined component-from prototype to full-scale production-meets the rigorous standards of the medical device industry.
Key Responsibilities:
  • Collaborate with design and manufacturing engineers to develop quality plans for new medical components.
  • Lead and participate in Design and Process FMEAs to identify and mitigate potential failure modes in CNC machining processes.
  • Oversee IQ/OQ/PQ activities for new equipment and validated processes.
  • Develop inspection methodologies for complex geometries, including the use of CMM, vision systems, and precision hand tools.
  • Ensure all project documentation complies with ISO 13485 and FDA 21 CFR Part 820 standards.
  • Work with raw material and coating suppliers to ensure incoming components meet technical specifications.
  • Utilize Six Sigma and Lean tools to optimize yields and reduce scrap during the transition from R&D to production.

Requirements
  • Bachelor's degree in mechanical engineering, industrial engineering, or a related technical field.
  • 3+ years of quality engineering experience within the medical device industry.
  • Strong understanding of GD&T (Geometric Dimensioning and Tolerancing) and its application in CNC machined parts.
  • Hands-on experience with ISO 13485 and the CAPA process.
  • Proficiency with statistical software (like Minitab) and experience with high-precision metrology equipment.
  • ASQ Certified Quality Engineer (CQE) or Six Sigma Green/Black Belt is a plus.

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