Quality Engineer I

Posted Yesterday
Be an Early Applicant
Dayton, OH, USA
In-Office
54K-84K Annually
Junior
Hardware • Healthtech • Manufacturing
The Role
Performs quality engineering activities for regulated medical device manufacturing, including risk management, PFMEAs, root cause investigations, corrective actions, validation and test method support, process controls, nonconforming product disposition, audits, customer complaints, and continual improvement. Develops quality documentation, analyzes production and validation data, supports ISO 13485 compliance, and collaborates with manufacturing, customers, and technical stakeholders.
Summary Generated by Built In
Overview

Resonetics is a global leader in advanced engineering, prototyping, product development, and micro manufacturing, driving innovation in the medical device industry. With rapid expansion across all our locations, we continue to push the boundaries of technology while fostering a dynamic, employee-centered culture. Our commitment to excellence and continuous improvement makes Resonetics an exciting place for professionals passionate about shaping the future of micro-manufacturing and being part of something bigger.


We are looking for a Quality Engineer I to join our growing team in Kettering, OH. This role applies Quality Engineering and scientific method techniques and principles to daily tasks and activities; applies relevant regulations, standards, and industry best practices to assignments; plans and conducts projects and assignments with moderate to high technical responsibility, complexity or strategic input; receives summarized instructions from technical Quality leaders at various levels in addition to other functional stakeholders. 



Join Resonetics and be part of a team that’s redefining medical device manufacturing. If you’re passionate about innovation and thrive in a fast-paced environment, we’d love to hear from you.

Responsibilities
  • Demonstrates proficiency in applying various tools and methods to identify and realize new product or process introductions (ex. QMS, product related), and business improvements. 
  • Developing Risk documentation such as PFMEAs in compliance with the QMS and regulatory standards. Contributes to the application of various risk management and risk mitigation tools and practices. 
  • Leads and/or contributes to root cause investigations using various problem-solving techniques and tools. Develop Corrective Action plans and assess for effectiveness. 
  • Conducts and supports the development of test methods (TMV / Gage R&R studies) in equipment, process, and product qualifications/validations. 
  • Develops, implements and/or maintains process controls & quality control plans in proportion to risk using appropriate techniques and tools (ex. Statistical process controls, statistical inspection sampling). 
  • Supports all levels of manufacturing per ISO 13485. 
  • Participates in design/technical reviews as appropriate. 
  • May act as a subject matter expert (SME) in audits. 
  • Liaising with customers to resolve issues and Customer Complaints. 
  • Generating process deviations & Customer Change Notices. 
  • Assisting with troubleshooting of production and product development processes. 
  • Ensuring QMS procedures and appropriate regulations and industry standards are being utilized throughout product and process development, and manufacturing. 
  • Dispositioning nonconforming product. 
  • Identifying and working on continual improvement projects. 
  • Author protocols and reports or provides support in performing related qualification activities. Analyzing production and validation data. 
Required Qualifications

1-3+ years’ experience in a Quality Engineering role in regulated Manufacturing environment with preference for experience with Medical Device.  

Ability to create job-related documentation for quality purposes. 

Demonstrated technical writing and communication skills. 

Working knowledge of Statistical software and/or Minitab. 

Bachelor’s degree in engineering or scientific discipline, or equivalent experience. 

Preferred Qualifications

Familiarity with ISO Quality Systems, particularly ISO13485.  

Use of optical inspection equipment. This may be defined as a magnifier, microscope, and/or equipment used for measuring capacity. 

Physical Demands

Light office work only; position may include up to 10% domestic and international travel. 

Standing and walking for short periods of time. 

Ability to use a microscope, including manipulating small objects under a microscope. 

Compensation
  • The compensation for this role is competitive and will be based on experience and qualifications. The anticipated range is $54,000–$84,000.
  • Our company policy is that we are unable to provide visa sponsorship. Candidates must already be legally authorized to work in the United States without the need for sponsorship now or in the future.

Resonetics offers a comprehensive benefits package designed to support the health, well-being, and financial security of our employees and their families. Benefits include medical, dental, and vision insurance; a 401(k) retirement plan; paid time off (PTO); 10 paid holidays; Flexible Spending Accounts (FSA); life and Accidental Death & Dismemberment (AD&D) insurance; Short-Term Disability (STD) and Long-Term Disability (LTD) insurance; accident, critical illness, and hospital indemnity insurance. Eligibility and benefit offerings may vary based on employment status and applicable plan provisions.

Skills Required

  • 1-3+ years of experience in a Quality Engineering role in a regulated manufacturing environment
  • Bachelor’s degree in engineering or a scientific discipline, or equivalent experience
  • Ability to create job-related documentation for quality purposes
  • Demonstrated technical writing and communication skills
  • Working knowledge of statistical software and/or Minitab
  • Familiarity with ISO quality systems, particularly ISO 13485
  • Experience with medical device manufacturing
  • Use of optical inspection equipment, such as magnifiers, microscopes, or measuring equipment

Resonetics Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Resonetics and has not been reviewed or approved by Resonetics.

  • Healthcare Strength — Healthcare coverage is described as solid, with broad coverage and in some cases day-one eligibility. Medical coverage is viewed as a dependable pillar of the total rewards package.
  • Leave & Time Off Breadth — Paid time off is commonly provided and taking time away is often described as straightforward, though administration can vary by site. This breadth offers a practical counterweight to concerns about base pay for some roles.
  • Retirement Support — Retirement benefits, including 401(k) features with immediate vesting in some cases, are highlighted as part of a comprehensive package. These elements strengthen long-term financial security beyond base wages.

Resonetics Insights

Am I A Good Fit?
beta
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

The Company
HQ: Nashua, NH
2,600 Employees
Year Founded: 1987

What We Do

Resonetics is a medical device contract development and manufacturing organization serving MedTech partners. Founded in Nashua, New Hampshire, it provides advanced engineering, prototyping, product development, micromanufacturing, sensor technologies, and value-added manufacturing. Its integrated services support medical-device innovation from ideation through commercialization, helping customers develop precise, scalable solutions and accelerate time to market. Its processes are designed for the precision and reliability required by life-critical medical devices.

Similar Jobs

Tosoh SMD, Inc. Logo Tosoh SMD, Inc.

Engineer I-Quality

Semiconductor • Chemical • Manufacturing • Solar
In-Office
43123, Grove City, OH, USA
185 Employees

Integra LifeSciences Logo Integra LifeSciences

Senior Engineer

Healthtech • Manufacturing
In-Office
Cincinnati, OH, USA
3489 Employees
71K-98K Annually

Revel Logo Revel

Controller

Aerospace • Hardware • Robotics • Software
In-Office or Remote
4 Locations
70 Employees

Digible Logo Digible

Senior Manager, Product Design

AdTech • Agency • Artificial Intelligence • Digital Media • Marketing Tech • Social Media • PropTech
Remote or Hybrid
United States
145 Employees
160K-190K Annually

Similar Companies Hiring

Ford Energy Thumbnail
Automotive • Software • Energy • Utilities • Manufacturing • Renewable Energy
Glendale, Kentucky
55 Employees
Revel Thumbnail
Aerospace • Hardware • Robotics • Software
Marina Del Rey, California
70 Employees
Unusual Machines, Inc. Thumbnail
Hardware • Robotics
Orlando, FL
300 Employees

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account