Cleanroom Technician

Cleanroom Technician

Medical Device | Long-Term Opportunity | Day Shift

The Cleanroom Technician supports process and product quality by preparing equipment, samples, and materials for testing, conducting environmental monitoring in clean rooms, and reviewing batch records from production. This role also partners with third-party testing laboratories to prepare devices for sterilization, interpret sterility data, and contribute to investigations of non-conformances. You play a key role in ensuring products meet strict quality and regulatory standards in a dynamic, small-company environment.

Responsibilities

• Perform environmental monitoring of clean rooms, including humidity and temperature checks and verification of pest control measures.
• Collect, prepare, and submit samples to various internal and external laboratories for further analysis.
• Verify and analyze test results to ensure they meet established specifications and quality system requirements.
• Prepare and mix chemical formulations for production and manufacturing use in accordance with SOPs.
• Execute in-process quality control tasks to monitor product and process performance during manufacturing.
• Maintain accurate maintenance records for all equipment used in quality control and production support.
• Perform daily pre-operational quality control checks of passivation chemistry to ensure proper performance.
• Conduct package visual inspections, seal strength testing, and integrity testing for sterile seals and pouching.
• Review sterilization certificates to determine readiness for full product release.
• Maintain accurate, complete, and organized records of all quality control activities and findings.
• Participate in quality control investigations and corrective and preventive actions (CAPAs) related to non-conformances.
• Verify that quality control measurements are accurate and document results with strong attention to detail.
• Ensure inspections are completed on time and aligned with production priorities and schedules.
• Review manufacturing records, including sterile processing data, test results, certifications, labeling, and paperwork to confirm compliance with specifications and quality system requirements.
• Perform batch record review for production lots to ensure completeness, accuracy, and adherence to procedures.
• Collaborate with third-party sterilization and contract testing laboratories by preparing devices for sterilization and entering sterility data into documentation systems.
• Support investigations by analyzing data from non-conformances and assisting in the development of investigation plans.
• Follow standard operating procedures consistently and escalate quality concerns when something appears out of scope.

Additional Skills & Qualifications

• Associates in Science is preferred, but not required.
• Prior cleanroom experience is a must
• Experience working with CAPA's and deviations is preferred.

Job Type & Location

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

Pay and Benefits

The pay range for this position is $56160.00 - $68640.00/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 11, 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 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.

If you would like to request a reasonable…