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Contract Medical Device Testing Jobs in Nebraska

embecta

Molding Processor

Holdrege, NE

embecta is a global medical device company with a 100-year legacy in insulin delivery and diabetes ... Perform required inspections, mold approvals, rejections, setup ofgaugesand leak testing.

embecta

Molding Processor

Holdrege, NE · On-site

embecta is a global medical device company with a 100-year legacy in insulin delivery and diabetes ... Perform required inspections, mold approvals, rejections, setup of gauges and leak testing.

Irhythmtech

Territory Manager | Nebraska

Omaha, NE · On-site

The ideal candidate has a proven track record in medical device sales, is highly strategic, goal ... Lead the full sales cycle, from lead generation and needs assessment to contract close and ...

Irhythmtech

Territory Manager | Nebraska

Lincoln, NE · On-site

The ideal candidate has a proven track record in medical device sales, is highly strategic, goal ... Lead the full sales cycle, from lead generation and needs assessment to contract close and ...

Danaher

Software Engineer Internships

Lincoln, NE · On-site

Participating on an Agile Scrum team, collaborating across design, development, and testing ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

Danaher

Software Engineer Internships

Grand Island, NE · On-site

Participating on an Agile Scrum team, collaborating across design, development, and testing ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

Danaher

Software Engineer Internships

Omaha, NE · On-site

Participating on an Agile Scrum team, collaborating across design, development, and testing ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

Danaher

Software Engineer Internships

Bellevue, NE · On-site

Participating on an Agile Scrum team, collaborating across design, development, and testing ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

Danaher

Software Engineer Internships

Kearney, NE · On-site

Participating on an Agile Scrum team, collaborating across design, development, and testing ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

Danaher

Participating on an Agile Scrum team, collaborating across design, development, and testing ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

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Showing results 21-40

All JobsContract Medical Device Testing JobsContract Medical Device Testing Jobs in Nebraska

Contract Medical Device Testing information

What is the difference between Contract Medical Device Testing vs Medical Device Quality Assurance Specialist?

AspectContract Medical Device TestingMedical Device Quality Assurance Specialist
CredentialsTypically requires technical testing certifications, knowledge of testing standardsRequires quality management system certifications, ISO 13485 knowledge
Work EnvironmentLaboratories, testing facilities, controlled environmentsManufacturing sites, quality departments, regulatory offices
Employer & Industry UsageContract testing labs, CROs, medical device companiesMedical device manufacturers, regulatory agencies

Contract Medical Device Testing focuses on performing specific tests to ensure device safety and compliance, often in labs or testing facilities. Medical Device Quality Assurance Specialists oversee quality systems, compliance, and regulatory adherence within manufacturing or corporate settings. While both roles require knowledge of industry standards, testing professionals concentrate on technical testing, whereas QA specialists focus on quality management and regulatory processes.

What are popular job titles related to Contract Medical Device Testing jobs in Nebraska? For Contract Medical Device Testing jobs in Nebraska, the most frequently searched job titles are:
What job categories do people searching Contract Medical Device Testing jobs in Nebraska look for? The top searched job categories for Contract Medical Device Testing jobs in Nebraska are:
What cities in Nebraska are hiring for Contract Medical Device Testing jobs? Cities in Nebraska with the most Contract Medical Device Testing job openings:
Contract Medical Device Testing jobs near you
Infographic showing various Contract Medical Device Testing job openings in Nebraska as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 18% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Automation Engineer

Medivative Technologies

Kimball, NE • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 3 days ago

Job description

We are committed to providing reasonable accommodations for individuals with disabilities in our job application process. If you need assistance or an accommodation during the application or recruitment process due to a disability, you may contact us at KEIrecruiting@Kimballelectronics.com. We will treat all requests for accommodations discreetly.*Note: There is no Visa sponsorship being offered for this position.Kimball Solutions does not accept agency resumes. Please do not forward resumes to any recruiting alias or employee. Kimball Solutions is not responsible for any fees related to unsolicited resumes.

Learn more about our medical contract manufacturing here: Kimball Medical Solutions

Benefits:
Kimball Solutions provides 3 weeks of PTO starting your 1st year in addition to 10 paid holidays. Potential for annual profit sharing bonus based on company performance. Major health, dental, vision, and complementary insurances offered starting day 1. We offer a 50% match on your first 6% of 401k contribution with opportunity for an employer contribution annually.

Quick Summary

As Automation Engineer, you will ensure that all automated manufacturing processes have alignment with the validation strategies and quality procedures. You will assist in the development of vision and programming standards and source code reviews for automated equipment. You will provide guidance to suppliers on new equipment builds, analyze production equipment performance and develop plans to increase yield from underperforming inspections.

The ability to manage projects that may compete for your time while keeping accurate records of work is crucial for this role. In our business, it is critical you can demonstrate a solid understanding of the importance of quality and documentation. You will be working with Allen Bradley PLC's, Cognex Vision systems, and Fanuc Robots. Mastery of at least one of those systems is preferred.

Basic Background Requirements:

  • 2+ years of experience in Automated Manufacturing.
  • Validation experience, process and equipment qualification (IQ,OQ,PQ), Test Methods are a plus.
  • Compose professional documentation (Write protocols, work instructions, engineering studies, etc.).
  • Manage time and projects effectively while setting and meeting ambitious schedules.
  • Knowledgeable on regulatory requirements, FDA 21 CFR 820/GMP Medical Device Regulations.
  • Working knowledge of Minitab.
  • Knowledge of statistical techniques and sampling for process validation and process monitoring is desired.

Key Performance Objectives:

Short Term: (0 to 3 months)

  • Learn Kimball Quality system requirements
  • Train on processes required to validate processes in the Kimball quality system
  • Build relationships with others
  • Begin training on the manufacturing line and the technology in use on the Automated Equipment
  • Maintain customer specific system documentation in support of FDA regulatory requirements

Midterm: (3 to 6 months)

  • Begin to audit current validations and identify solutions
  • Develop an understanding of completing engineering changes on the Automated Equipment and maintaining the validated state of the equipment
  • Learn and adopt Kimball Electronics philosophies and culture

Long term: (6 to 12 months)

  • Identify process improvement areas and develop a plan to implement those improvements
  • Write and complete test method validation and equipment qualifications
  • Demonstrate understanding of and attend training to FDA 21 CFR 820/GMP Medical Device Regulations
Don't meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Kimball Solutions we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!We're proud to be an equal opportunity employer and consider qualified applicants without regard to race, color, religion, sex, national origin, ancestry, age, genetic information, sexual orientation, gender identity, marital or family status, veteran status, medical condition or disability or any other characteristic protected by applicable federal, state, or local law.We will consider for employment qualified candidates with arrest and conviction records, consistent with applicable law (including, for example, the San Francisco Fair Chance Ordinance for roles based in San Francisco).

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