Medical Device Lab Technologist

Quality Control Technician

As a Quality Control Technician, you will play a pivotal role in supporting process and product quality testing. Your responsibilities will include preparing equipment, samples, and materials for analysis, as well as performing environmental monitoring in clean rooms. You will also partner with third-party testing laboratories and manage batch record reviews, non-conformance investigations, and data entry.

Responsibilities

+ Perform incoming, in-process, final, and finished product inspections.

+ Conduct measurement and verification activities using calibrated inspection equipment.

+ Review manufacturing documentation, supplier-provided data, and Certificates of Analysis.

+ Verify product labeling, packaging, and acceptance criteria.

+ Identify, document, and control nonconforming materials and products.

+ Maintain quarantine areas and segregate returned products to prevent unintended use.

+ Prepare samples, submit them for analysis, collect and analyze data, and interpret results.

+ Perform environmental monitoring of clean rooms.

+ Collect, prepare, and submit samples to various labs.

+ Verify and analyze test results.

+ Prepare and mix chemical formulations for production use.

+ Perform in-process quality control tasks and maintain equipment maintenance records.

+ Conduct daily pre-operational QC checks of passivation chemistry.

+ Perform package visual inspection, seal strength, and integrity testing.

+ Review sterilization certificates for full release.

+ Engage in QC investigations and corrective action plans (CAPAs).

Essential Skills

+ 4+ years of quality experience in a regulated industry (medical device, pharmaceutical, cosmetic, aerospace, food).

+ Ability to follow Standard Operating Procedures (SOPs) and demonstrate a quality mindset.

+ 1+ years of experience in investigation, technical reports, and analysis.

Additional

Skills & Qualifications

+ Associates or Bachelors degree in science.

+ Experience in the medical device industry.

+

Experience with third-party sterilization labs or contract testing labs.

+ 6+ months of sterilization/environmental monitoring experience in a regulated environment.

Work Environment

This position is fully on-site operating from 8:00 AM to 4:30 PM, Monday through Friday. The role is primarily focused on quality control functions (80%) with the remaining time dedicated to documentation tasks (20%).

Job Type & Location

This is a Permanent position based out of Saint Paul, MN.

Pay and Benefits

The pay range for this position is $52000.00 - $62400.00/yr.

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.

Benefits include medical, dental, vision and life insurance. Additionally they offer a 401K, with company match of up to 4%. They also have profit sharing

Workplace Type

This is a fully onsite position in Saint Paul,MN.

Final date to receive applications

This position is anticipated to close on Oct 19, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a Clearly Rated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all…