At TÜV SÜD Group we are passionate about technology. Innovations impact our daily lives in countless ways, and we are dedicated to being a part of that progress. We test, we audit, we inspect, we advise. We never stop challenging ourselves for the safety of society and its people. We breathe technology, we strive for professional excellence, and we leave a mark. We take the future into our hands. We are TÜV SÜD Group.

Your Tasks

• Execute reprocessing validation studies, including cleaning validation (manual and automated), disinfection efficacy, drying time assessments, and simulated‑use lifecycle testing.
• Prepare test articles by performing soiling, inoculation, assembly/disassembly, and related preparation steps to ensure standardized test conditions.
• Operate and maintain laboratory equipment such as washer‑disinfectors, sterilizers, and drying systems in alignment with applicable standards (e.g., ISO 17664, ISO 15883, AAMI TIR12/TIR30).
• Document all laboratory work accurately and consistently in accordance with GLP and ISO 17025 requirements.
• Identify deviations, unexpected results, or equipment issues and communicate them promptly to Study Directors or the Biological Team Lead.
• Support equipment qualification, calibration, and general laboratory upkeep to maintain a safe and compliant workplace.
• Collaborate with cross‑functional teams to support study timelines and contribute to continuous improvement initiatives.

Your Qualifications

• High school diploma or equivalent.
• 0–3 years of laboratory experience (medical device, pharmaceutical, or microbiology preferred).
• Basic understanding of microbiology principles, contamination control, and aseptic technique.
• Ability to follow detailed procedures with accuracy, strong attention to detail, and comfort working in regulated environments.
• Proficiency in Microsoft Office and willingness to learn laboratory software and equipment systems.
• Experience working within GLP or ISO 17025 environments.
• Prior hands‑on experience with medical device testing or reprocessing technologies.
• Strong communication and teamwork skills, including the ability to work independently with guidance.

What We Offer

• A collaborative environment that promotes learning, development, and hands‑on technical growth.
• Opportunities to work with advanced testing equipment in a regulated laboratory setting.
• Global company resources supporting training, compliance, safety, and continuous improvement.

Additional Information

• The anticipated hourly base pay range for this full-time position is $21/hour - $26/hour. Actual base pay will be determined based on various factors, including years of relevant experience, training, qualifications, and internal equity. Additionally, we offer a comprehensive benefits package to employees, including a 401(k) plan with employer match, up to 12 weeks of paid parental leave for birthing parents and 2 weeks for other parents, health plans (medical, dental, and vision), life insurance and disability, and generous paid time off.
• Work model: On-site at our New Brighton Laboratory.
• We welcome applications from people of all backgrounds, experiences, and perspectives.

Equal Opportunity Employer - Disability and Veteran

TÜV SÜD America, Inc. is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, creed, religion, ancestry, marital status, genetics, national origin, sex, sexual orientation, gender identity and expression, age, physical or mental disability, veteran status and those laws, directives, and regulations of Federal, State, and Local governing bodies or agencies. We participate in the E-Verify Employment Verification Program.