Quality Control Technician 2 - PTL

MerckJaffrey, NH
2d$19 - $30Onsite

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 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.

Requirements

  • 1+ years of laboratory or cGMP manufacturing experience.
  • High school diploma or GED.

Nice To Haves

  • Associate’s degree in any discipline.
  • 2+ years of 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.

Responsibilities

  • 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.

Benefits

  • Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites.
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