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Assistant Biomedical Engineering Fresh Graduate Jobs in Milwaukee, WI

Validation Engineer

Hartland, WI · On-site

$73K - $110K/yr

Perform engineering studies to determine if projects are feasible. * Assist with measurement system ... Masters of Science in Chemistry, Biology, Biotechnology, Chemical Manufacturing, Biomedical ...

Perform engineering studies to determine if projects are feasible. * Assist with measurement system ... Masters of Science in Chemistry, Biology, Biotechnology, Chemical Manufacturing, Biomedical ...

Validation Engineer

Hartland, WI · On-site

$73K - $110K/yr

Perform engineering studies to determine if projects are feasible. Assist with measurement system ... Manufacturing, Biomedical Engineering, or Engineering. Six Sigma certification. 3 years of ...

Validation Engineer

Hartland, WI · On-site

$73K - $110K/yr

Perform engineering studies to determine if projects are feasible. * Assist with measurement system ... Masters of Science in Chemistry, Biology, Biotechnology, Chemical Manufacturing, Biomedical ...

We are looking for a student who is enrolled in civil engineering, undergraduate or graduate ... ESSENTIAL DUTIES Assist with daily tasks that might involve: Assist engineering staff with building ...

Dental assistant

Milwaukee, WI · On-site

$18 - $23/hr

Open for fresh graduates. Bilingual, Trainable, Personable Title Dental assistant We are seeking a ... Whether you're a recent graduate or an experienced dental assistant, we welcome your application.

Dental assistant

Milwaukee, WI · On-site

$18 - $23/hr

Open for fresh graduates. Bilingual, Trainable, Personable Title Dental assistant We are seeking a ... Whether you're a recent graduate or an experienced dental assistant, we welcome your application.

Showing results 21-40

Assistant Biomedical Engineering Fresh Graduate information

See Milwaukee, WI salary details

$5

$19

$32

How much do assistant biomedical engineering fresh graduate jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for assistant biomedical engineering fresh graduate in Milwaukee, WI is $19.26, according to ZipRecruiter salary data. Most workers in this role earn between $14.90 and $21.06 per hour, depending on experience, location, and employer.

What does an assistant biomedical engineering fresh graduate do?

An Assistant Biomedical Engineering Fresh Graduate typically supports senior engineers in designing, developing, and testing medical devices and equipment. Their responsibilities may include assisting with research projects, analyzing data, preparing technical reports, and ensuring compliance with healthcare regulations. They often work closely with multidisciplinary teams in hospitals, research labs, or medical device companies to improve patient care through technology. This entry-level role provides valuable hands-on experience and opportunities to learn about the biomedical engineering field.

What typical projects or tasks might an assistant biomedical engineering fresh graduate be assigned in their first year?

As an Assistant Biomedical Engineering Fresh Graduate, you can expect to be involved in a variety of entry-level projects such as assisting with the maintenance and calibration of medical equipment, supporting the design and testing of new medical devices, and participating in quality assurance activities. You may also help senior engineers with data collection, documentation, and regulatory compliance tasks. Collaboration with clinical staff, technicians, and other engineers is common, providing valuable exposure to multidisciplinary teamwork and practical problem-solving.

What are the key skills and qualifications needed to thrive as an assistant biomedical engineering fresh graduate, and why are they important?

To thrive as an Assistant Biomedical Engineering Fresh Graduate, you need a solid understanding of engineering principles, biology, and medical device fundamentals, typically supported by a relevant bachelor's degree. Familiarity with CAD software, laboratory instruments, and industry standards such as ISO 13485 is often required. Strong problem-solving abilities, teamwork, and effective communication skills set candidates apart in this field. These skills and qualities are critical for developing safe, innovative healthcare solutions and for successful collaboration within multidisciplinary teams.

What is the difference between Assistant Biomedical Engineering Fresh Graduate vs Biomedical Equipment Technician?

AspectAssistant Biomedical Engineering Fresh GraduateBiomedical Equipment Technician
Required CredentialsBachelor's degree in Biomedical Engineering or related fieldAssociate's degree or certification in biomedical equipment technology
Work EnvironmentHospitals, research labs, medical device companiesMedical facilities, service centers, hospitals
Employer & Industry UsageUniversities, healthcare institutions, medical device firmsHospitals, clinics, biomedical service providers

The Assistant Biomedical Engineering Fresh Graduate typically holds a bachelor's degree and supports engineering projects, while the Biomedical Equipment Technician focuses on maintaining and repairing medical equipment, often requiring specialized certifications. Both roles operate in healthcare settings but differ in responsibilities and qualifications.

What cities near Milwaukee, WI are hiring for Assistant Biomedical Engineering Fresh Graduate jobs?

Cities near Milwaukee, WI with the most Assistant Biomedical Engineering Fresh Graduate job openings:

Infographic showing various Assistant Biomedical Engineering Fresh Graduate job openings in Milwaukee, WI as of June 2026, with employment types broken down into 6% Internship, 65% Full Time, and 29% Part Time. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $40,071 per year, or $19.3 per hour.

Validation Engineer

Medline

Hartland, WI • On-site

$73K - $110K/yr

Full-time

Medical, Life, Retirement, PTO

Re-posted yesterday


Medline Industries rating

7.5

Company rating: 7.5 out of 10

Based on 250 frontline employees who took The Breakroom Quiz

233rd of 544 rated manufacturers


Job description

Job Summary
Responsible for the validation of facility utilities, and equipment processes for cGMP products such as pharmaceuticals, medical devices, and cosmetic products to adhere to 21 CFR 211/210, 21 CFR 820, and other applicable regulatory requirements. Assist in authoring and executing protocols to demonstrate that manufacturing processes are executed with consistent quality and results within a controlled environment. Responsible for managing and or performing revalidation, engineering studies to evaluate new products or components, change control assessments, and coordination of computer and test method validations of applicable products.
Job Description
  • Validate new and revalidate as appropriate existing equipment used in OTC/Cosmetic and medical device manufacturing.
  • Perform engineering studies to determine if projects are feasible.
  • Assist with measurement system analysis including Gage R&R.
  • Support product/design transfer activities including validations and creation of updates to documentation needed to manufacture OTC cosmetic and medical devices.
  • Support Change Assessment activities including assessment and qualification of changes to existing product components and implementation of products into manufacturing lines.
  • Support root cause investigations for non-conformances related to manufacturing validations.
  • Develop, prepare and install equipment and revise test validation procedures/protocols to ensure that a product is manufactured in accordance with appropriate regulatory agency validation requirement and current industry practices.
  • Responsible for IQ/OQ and PQ phases and implementation of validated SOPs.
  • Coordinate projects directly with vendors and service providers to ensure that all validation and installation requirements are being satisfied during the execution of protocols.
  • Develop timelines for all projects and ensure that deadlines and goals are being met. Frequently update management and team on progress.
  • Proactively work with members of the division or project team to identify issues that might delay the project; make recommendations to improve time lines for project completion.
  • Compile and analyze validation data, prepare reports, and make recommendations for changes and/or improvements.
  • Maintain all of the documentation pertaining to qualification and validation of assigned projects and equipment/systems.

REQUIRED EXPERIENCE
Education
  • Bachelor of Science Degree in Biology, Chemistry, or Engineering.

Work Experience
  • At least 2 years of validation experience in a cGMP Device or Drug environment.
  • Experience with validations of controlled environments or equipment validations in a regulated environment.
  • Experience with validation documentation and related change control.
  • Strong ability to manage multiple priorities, self-starter attitude, good oral and writing skills and the ability to work independently and as a team in an efficient manner.

PREFERRED QUALIFICATIONS
  • Masters of Science in Chemistry, Biology, Biotechnology, Chemical Manufacturing, Biomedical Engineering, or Engineering.
  • Six Sigma certification.
  • 3 years of validation experience in a cGMP Device or Drug environment.
  • Process validation experience in a pharmaceutical or Medical Device manufacturing environment.
  • Experience with validation of various product types such as liquid products, solid dosage products, and multi-component products.
  • Experience in FDA regulated environment.
  • Experience with ISO 13485 and ISO 11607 standards.
  • Experience with Measurement System Analysis.
  • Experience with Minitab statistical analysis software.
  • Experience with root cause analysis.

Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.
The anticipated salary range for this position:
$73,000.00 - $110,000.00 Annual
The actual salary will vary based on applicant's location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold.
Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions, paid time off, as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. For a more comprehensive list of our benefits please click here.
We're dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here.
Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.

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About Medline

Sourced by ZipRecruiter

Medline Industries, LP is the leading nationwide supplier of medical, surgical and pharmaceutical products to hospitals, nursing homes, HME providers, surgery centers, physician offices and home care/hospice settings.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Winnetka, IL, US

Year founded

1966