Technical Associate

Overview

At QIAGEN, we are driven by a simple but powerful vision: making improvements in life possible.

We're dedicated to revolutionizing science and healthcare for the better. From our entrepreneurial roots to our current global presence, we've grown into a force for positive change. With thousands of employees across six continents, collaboration is our greatest strength. We're always striving to identify talented individuals to join our exceptional teams.

We have played a pivotal role in shaping modern science and healthcare, and we're just getting started. If you're someone who thrives on new challenges, values diversity and wants to make a tangible difference in people's lives, then QIAGEN is the place for you.

At QIAGEN, every day is an opportunity to make a real-life impact.

Join us, grow with us, and together, let's shape the future of biological discovery.

About the opportunity

This role offers the opportunity to contribute directly to QIAGEN's manufacturing operations by supporting the labeling of vialed materials and the assembly of diagnostic kits. The position plays a key role in ensuring products are prepared in compliance with regulatory requirements such as QSR, ISO, OSHA, IVDD, and MDD, as well as internal Standard Operating Procedures. Working in a fast-paced laboratory environment, the role supports high-quality manufacturing output through accurate execution of procedures, clear communication, and careful documentation.

This is a 6-week, short term assignment.

Your tasks include

• Performing labeling of vialed materials and assembly of kits in accordance with applicable regulations and SOPs.
• Comprehending and executing manufacturing processes as defined in SOPs and Manufacturing Master Records (MMRs).
• Completing hands-on production activities such as racking, counting, labeling, and packaging of materials.
• Communicating material needs to inventory personnel and reporting issues or discrepancies to supervisors.
• Carrying out daily cleaning and disinfection of laboratory areas and associated equipment.
• Completing production documentation accurately and efficiently, including material inspections and verification of materials used in manufacturing processes.

Your profile

• High School Diploma or equivalent, with 0-2 years of related work experience.
• Ability to use equipment, materials, and time efficiently in a manufacturing environment.
• Capability to write, complete, and maintain MMRs and other production-related documentation.
• Confidence in communicating issues, deviations, or problems to supervisors.
• Basic math skills and strong attention to detail.
• Proficiency in spoken and written English.
• Ability to lift up to 50 lbs and perform tasks requiring manual dexterity.
• Comfort working in a fast-paced environment with changing priorities and exposure to potentially biohazardous and/or chemically hazardous materials.

The typical pay rate for this role is $18/hour.

What we offer

• Bonus/Commission

• Local benefits

• Referral Program

• Volunteer Day

• Internal Academy (QIALearn)

• Employee Assistance Program

• Hybrid work (conditional to your role)

Our people are the heartbeat of everything we do. Passion drives us as we push boundaries to innovate and evolve. We inspire with our leadership and make an impact with our actions. We cultivate a collaborative, supportive environment where each individual and team can flourish. We champion accountability and encourage entrepreneurial thinking.

QIAGEN is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, or disability.