Test Technician

Actalent; Maple Grove (MN); On-site; USD 41,000 - 55,000; Full time

Benefits offered by this job

Medical insurance

401(k) plan

Life Insurance

Disability insurance

HSA

Transit benefits

Employee Assistance Program

Paid time off

Job summary

Actalent is seeking an R&D Test Technician in Maple Grove, MN, to support engineers by building, testing, and troubleshooting medical devices and fixtures. You’ll contribute to design verification, process validation, and product development within a regulated environment.

The role emphasizes hands-on testing, documentation accuracy, and collaboration with cross-functional teams, ensuring quality and compliance in prototype builds and test setups.

Qualifications

• 1-2 year technical degree or certification in mechanical, electrical, biomedical, or related engineering tech field.
• 3+ years in medical device R&D/testing/manufacturing support.
• Strong proficiency with hand tools and measurement devices; ability to troubleshoot.
• Experience performing documented testing in a regulated medical device environment.
• Ability to read and interpret drawings, schematics, and work instructions.
• Proficient with test equipment and data acquisition for validation.
• Capable of calibration and basic repair of fixtures/test setups.
• Attention to detail and accurate documentation for quality/regulatory.
• Clear communication and cross-functional teamwork.
• Comfort with electro-mechanical devices in a process-driven setting.

Responsibilities

• Build and assemble electro-mechanical medical devices and fixtures per drawings and work instructions.
• Set up and document test methods to support design verification and process validation.
• Test capital equipment and single-use devices, including in-water tests.
• Assemble, calibrate, and verify performance using hand tools and measurement devices.
• Troubleshoot issues, identify root causes, and implement corrective actions with engineers and QA.
• Read and interpret engineering drawings and test methods at required levels.
• Maintain test records, logs, calibration records, and other quality documentation.
• Contribute to test method refinement to improve clarity and efficiency.
• Assist with fixture assembly, repair, and maintenance to keep equipment functional.
• Collect and analyze test data with data acquisition tools; support improvements.
• Collaborate with R&D, engineering, QA, and manufacturing for product development.
• Work independently, prioritize tasks, and meet testing and build schedules.
• Maintain clean, safe work area per lab and site procedures.

Skills

Tech degree/cert

3+ years medical device exp

Hand tools & measurement tools

Read drawings & schematics

Troubleshooting

Data acquisition

Cross-functional collaboration

Documentation accuracy

Regulated environment

Effective communication

Education

2-year technical degree

Tools

Test equipment

Calibration tools

Scripting for automated tests

Job description

Job Title: R&D Test Technician Job Description
The R&D Test Technician will support the engineering team by performing hands-on build, assembly, testing, and troubleshooting of medical devices and associated fixtures. This role plays a key part in delivering high-quality prototype builds, executing precise tests, and maintaining reliable documentation to support design verification, process validation, and product development activities. The position suits an experienced, detail-oriented technician who thrives in a regulated medical device environment and collaborates effectively with engineers, quality professionals, and manufacturing teams. You will contribute directly to the development of a state-of-the‑art device designed to provide minimally invasive therapy for prostate cancer, which has received U.S. FDA Breakthrough Device Designation.

Responsibilities

• Build and assemble electro‑mechanical medical devices, prototypes, and associated fixtures according to engineering drawings, schematics, and work instructions.
• Set up, execute, and document test methods to support design verification, process validation, and ongoing product development activities.
• Perform hands‑on testing on capital equipment, including tests conducted under water, as well as on single‑use medical devices.
• Use hand tools, measurement tools, and test equipment to assemble, calibrate, and verify the performance of devices and fixtures.
• Troubleshoot mechanical and electro‑mechanical issues, identify root causes, and support implementation of corrective actions in collaboration with engineering and quality teams.
• Read and interpret engineering drawings, blueprints, schematics, test methods, and work instructions at or above an 8th‑grade reading level to ensure accurate build and test execution.
• Review and complete documentation accurately, including test records, build logs, calibration records, and other quality‑related documentation in compliance with regulated environment requirements.
• Support the development, review, and refinement of test methods and work instructions to improve clarity, repeatability, and efficiency.
• Assist with fixture assembly, repair, and maintenance to ensure test equipment remains functional, calibrated, and safe to use.
• Use data acquisition tools and test instrumentation to collect, monitor, and record test data, and support analysis of results.
• Collaborate with cross‑functional teams including R&D, engineering, quality, and manufacturing to support product development and continuous improvement.
• Work independently to prioritize tasks, follow schedules, and complete assigned testing and build activities on time.
• Maintain a clean, organized, and safe work area, following laboratory and facility procedures for handling equipment and materials.

Essential Skills

• 1 or 2‑year technical degree or certification in mechanical, electrical, biomedical, or related engineering technology field.
• 3+ years of experience working in medical device companies in an R&D, engineering, testing, or manufacturing support role.
• Strong proficiency with hand tools, measurement tools, fixture assembly, and mechanical troubleshooting.
• Experience performing documented testing in a regulated environment, preferably within medical devices.
• Ability to read and interpret engineering drawings, test methods, schematics, blueprints, and work instructions.
• Proficiency using test equipment and measurement devices for validation and verification activities.
• Ability to perform calibration and basic repair of fixtures and test setups as needed.
• Strong attention to detail, organization, and documentation accuracy to support regulatory and quality requirements.
• Effective communication skills and ability to work both independently and within cross‑functional teams.
• Comfort working with electro‑mechanical devices and systems in a structured, process‑driven environment.

Additional Skills & Qualifications

• Experience building electro‑mechanical devices or systems, including capital equipment and single‑use devices.
• Familiarity with tolerance stack‑ups and geometric dimensioning and tolerancing (GD&T).
• Exposure to basic machining or 3D printing processes for prototype or fixture fabrication.
• Experience with data acquisition tools and test instrumentation to support automated or semi‑automated testing.
• Familiarity with scripting or basic programming to support automated testing workflows.
• Experience with documentation review and validation activities related to test methods and work instructions.
• Ability to support troubleshooting and repair of test equipment and fixtures in a laboratory or R&D environment.

Work Environment

This role is 100% on‑site in a regulated medical device development environment. You will work primarily in laboratory and engineering spaces, performing testing on capital equipment, including tests conducted under water, as well as on single‑use medical devices. The position requires frequent use of hand tools, measurement tools, test equipment, and data acquisition systems, along with regular interaction with engineering, quality, and manufacturing teams. You will work independently for significant portions of the day, following written test methods and work instructions, and are expected to read and understand documentation at or above an 8th‑grade level. The environment emphasizes safety, cleanliness, and organization, with adherence to established procedures and quality system requirements. Dress will align with typical laboratory and engineering settings, including appropriate attire and any required personal protective equipment as defined by site procedures.

Job Type & Location

This is a Contract to Hire position based out of Maple Grove, MN.

Pay and Benefits

The pay range for this position is $30.00 - $40.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job‑related factors. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms.

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan Pre‑tax and Roth post‑tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long‑term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Application Deadline

This position is anticipated to close on Oct 12, 2026.

Equal Opportunity Statement

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

Accommodation Assistance

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [e-mail] for other accommodation options.

San Francisco Fair Chance Ordinance

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI)

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.