Quality Control Technician 3- PTL

The businesses of Merck KGaA, Darmstadt, Germany•Jaffrey, NH

23h•$19 - $30•Onsite

About The Position

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! 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 The Quality Control Technician 3 is an advanced-level laboratory professional responsible for supporting the physical testing of biopharmaceutical filtration devices. This role focuses on ensuring safety, quality, and productivity throughout testing operations. The technician performs advanced-level testing tasks, including preparing membranes and devices, conducting tests, and troubleshooting issues as needed. They use the Laboratory Information Management System (LIMS) to track and manage test data, and carry out all work in strict accordance with Standard Operating Procedures (SOPs), Quality and Safety Specifications, and Good Manufacturing Practices (GMP). Duties include: Follow procedures to perform required device testing independently. Safely set up and operate quality lab test equipment and monitor required inputs and outputs on equipment such as pressurized vessels, steam equipment, and various test stands and support equipment. Support quality lab operations and projects under the guidance of master and lead technicians. Accurately complete and review documentation per GMP standards. Initiate and participate in Out of Specification (OOS) investigations. Support execution of protocols, qualifications, and validations. Ensure a clean and orderly workspace. Proactive identification of safety, quality, and productivity concerns. Actively report hazardous conditions or hazardous behaviors observed in the work environment and the site. Participates in laboratory audits and tours, performs troubleshooting and advanced test set-ups, reviews and verifies test and process data with accurate entry into the Laboratory Information Management System, supports sustainability initiatives, and works effectively under limited supervision. B shift position Monday - Friday 2pm-10pm Physical Attributes Exposure to machinery, chemical reagents, and equipment in a laboratory environment. 100% Standing and/or sitting for duration of shift, up to 12 hours. Occasional lifting of 20 - 30 lbs. necessary/Max lifting – 40 to 50 lbs. Bend and twist as needed. Grasp, manipulate and handle objects consistently and regularly, Fine motor skills are required.

Requirements

3+ years of laboratory experience.
High school diploma or GED.

Nice To Haves

Strong knowledge of EHS, ISO, cGMP, and other laboratory and regulatory requirements.
Associate’s degree in a STEM field
3+ years’ experience in a cGMP laboratory environment.
1+ years of experience with Laboratory Information Management Systems.
Demonstrated computer skills, familiarity with Microsoft Office applications.
Reliable and self-motivated.
Read, follow and understand Test Methods, Test Specifications, and other technical documentation.
Certified trainer or equivalent.

Responsibilities

Follow procedures to perform required device testing independently.
Safely set up and operate quality lab test equipment and monitor required inputs and outputs on equipment such as pressurized vessels, steam equipment, and various test stands and support equipment.
Support quality lab operations and projects under the guidance of master and lead technicians.
Accurately complete and review documentation per GMP standards.
Initiate and participate in Out of Specification (OOS) investigations.
Support execution of protocols, qualifications, and validations.
Ensure a clean and orderly workspace.
Proactive identification of safety, quality, and productivity concerns. Actively report hazardous conditions or hazardous behaviors observed in the work environment and the site.
Participates in laboratory audits and tours, performs troubleshooting and advanced test set-ups, reviews and verifies test and process data with accurate entry into the Laboratory Information Management System, supports sustainability initiatives, and works effectively under limited supervision.