MilliporeSigma
Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.
Your Role We are seeking an Intermediate Physical Test Lab Quality Control Technician to support the full operation of testing biopharmaceutical filtration devices. This role focuses on maintaining the highest standards of safety, quality, and productivity while performing routine and intermediate-level testing activities. The technician will assist with test process setup, perform basic troubleshooting to ensure smooth operations, and utilize Laboratory Information Management Systems (LIMS) to support accurate data tracking and reporting.
Duties Include
Safely perform product testing in compliance with SOPs, GMP, and quality and safety standards.
Set up, operate, and monitor laboratory test equipment, including pressurized vessels, steam systems, and test stands.
Complete accurate paper and electronic documentation in accordance with GMP requirements.
Perform basic troubleshooting, equipment set‑ups, and support test execution under close supervision.
Review, verify, and accurately enter test and process data into the Laboratory Information Management System (LIMS).
Support laboratory operations, projects, protocols, qualifications, and validation activities alongside senior technicians.
Participate in Out‑of‑Specification (OOS) investigations and proactively identify safety, quality, and productivity concerns.
Maintain a clean, organized workspace and contribute to sustainability and continuous improvement efforts.
Physical Attributes
Exposure to machinery and equipment, chemical reagents, biological materials at Biosafety Levels 1 and 2, in a laboratory environment.
100% standing and/or sitting for the duration of shift, up to 12 hours.
Frequent lifting of 20–30 lbs. necessary; maximum lifting – 40–50 lbs.
Bend and twist as needed.
Grasp, manipulate and handle objects consistently and regularly; fine‑motor skills are required.
Minimum Qualifications
1+ year laboratory or cGMP manufacturing experience.
High school diploma or GED.
Preferred Qualifications
Associate’s degree in any discipline.
2+ years laboratory or cGMP manufacturing experience.
Basic knowledge of EHS, ISO, cGMP, and other manufacturing regulatory requirements.
Basic computer skills, familiarity with Microsoft Office applications.
Reliable and self‑motivated.
Read, follow and understand operating procedures and documentation.
Pay Range $19 – $30 per hour (based on location, level of experience, education, skill and other job‑related factors. Position may be eligible for sales or performance‑based bonuses.)
Benefits Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites.
What We Offer We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science & tech. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply Now Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
Seniority level
Entry level
Employment type
Full-time
Job function
Quality Assurance and Science
#J-18808-Ljbffr
This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.
Your Role We are seeking an Intermediate Physical Test Lab Quality Control Technician to support the full operation of testing biopharmaceutical filtration devices. This role focuses on maintaining the highest standards of safety, quality, and productivity while performing routine and intermediate-level testing activities. The technician will assist with test process setup, perform basic troubleshooting to ensure smooth operations, and utilize Laboratory Information Management Systems (LIMS) to support accurate data tracking and reporting.
Duties Include
Safely perform product testing in compliance with SOPs, GMP, and quality and safety standards.
Set up, operate, and monitor laboratory test equipment, including pressurized vessels, steam systems, and test stands.
Complete accurate paper and electronic documentation in accordance with GMP requirements.
Perform basic troubleshooting, equipment set‑ups, and support test execution under close supervision.
Review, verify, and accurately enter test and process data into the Laboratory Information Management System (LIMS).
Support laboratory operations, projects, protocols, qualifications, and validation activities alongside senior technicians.
Participate in Out‑of‑Specification (OOS) investigations and proactively identify safety, quality, and productivity concerns.
Maintain a clean, organized workspace and contribute to sustainability and continuous improvement efforts.
Physical Attributes
Exposure to machinery and equipment, chemical reagents, biological materials at Biosafety Levels 1 and 2, in a laboratory environment.
100% standing and/or sitting for the duration of shift, up to 12 hours.
Frequent lifting of 20–30 lbs. necessary; maximum lifting – 40–50 lbs.
Bend and twist as needed.
Grasp, manipulate and handle objects consistently and regularly; fine‑motor skills are required.
Minimum Qualifications
1+ year laboratory or cGMP manufacturing experience.
High school diploma or GED.
Preferred Qualifications
Associate’s degree in any discipline.
2+ years laboratory or cGMP manufacturing experience.
Basic knowledge of EHS, ISO, cGMP, and other manufacturing regulatory requirements.
Basic computer skills, familiarity with Microsoft Office applications.
Reliable and self‑motivated.
Read, follow and understand operating procedures and documentation.
Pay Range $19 – $30 per hour (based on location, level of experience, education, skill and other job‑related factors. Position may be eligible for sales or performance‑based bonuses.)
Benefits Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites.
What We Offer We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science & tech. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply Now Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
Seniority level
Entry level
Employment type
Full-time
Job function
Quality Assurance and Science
#J-18808-Ljbffr