New · posted Oct 16
LGC Group · Medical Devices
QC Technologist I
- Cumberland, ME
- On-site
- Full-time
- Associate & Specialist
Open until filled
The role
As a QC Technologist I at LGC, you will a key role in ensuring the success of our products and customers. You will follow standardized procedures and prepares samples for testing. Analyzes test results for accuracy, acceptability, and critical limits. This role relies on limited independent judgment to plan and accomplish goals. Performs a variety of tasks. A limited degree of creativity and latitude is required.
What you need
- Associates in Medical Laboratory Science or a Bachelor’s degree in Medical Technology (preferred) or related science degree (i.e. biology, chemistry, biochemistry)
- 1-3 years working experience in a clinical chemistry lab or equivalent setting
- Organization and multitasking skills
- Experienced in use of various software programs
- Previous working experience with mainstream clinical analyzers from Roche, Siemens, OrthoClinical, Beckman Coulter, or Abbott desired.
All your information will be kept confidential according to EEO guidelines.
What you'll do
Functional responsibilities include, but are not limited to, the following
- Operation of automated clinical analyzers
- Occasional data entry as well as assessment and interpretation of results
- Testing production and research & development samples and assessing testing results
Team responsibilities include, but are not limited to, the following
- Focus on customer service
- Problem solving, including ability to reprioritize and adjust workload as needed
- Working with Production and R&D personnel to ensure efficient use of reagents and analyzers
- Able to evaluate processes for inefficiencies and suggest improvements
- Attention to detail
- Able to work independently and as part of a team
Where you'll work
Cumberland, MEOn-siteOpen in Maps (opens in a new tab)
More jobs in Cumberland, ME
From the posting
About LGC Group
ABOUT LGC CLINICAL DIAGNOSTICS
LGC Clinical Diagnostics develops and manufactures a comprehensive portfolio of catalogue and custom-developed diagnostic quality solutions and component materials for the extended life sciences industry. We partner with IVD assay developers, pharmaceutical, CRO and academic institutions in commercialization activities across the entire diagnostic pipeline. Laboratorians and diagnostic professionals across disciplines of clinical chemistry, immunochemistry, serology, molecular diagnostics, and clinical genomics rely on LGC’s products to support accurate and reliable diagnostic results.
Our operating entities include Maine Standards Company, SeraCare Life Sciences, and Technopath Clinical Diagnostics, which are in vitro diagnostics (IVD) manufacturers of quality measurement tools (calibrators, controls, linearity, EQA/PT, biological materials), the Native Antigen Company, which is a manufacturer and supplier of viral antigens and LGC Proficiency Testing a global leader in PT schemes. We operate FDA-registered and ISO 13485-accredited facilities in Maine (USA), Massachusetts (USA), Maryland (USA), Tipperary (Ireland), ISO 9001-accredited facility in Oxford, UK, and Traverse City, Michigan US.
Each day, our world-class staff, scientific expertise, operational efficiency, and superior quality systems are ready to support the range of advanced technologies that collectively improve patient outcomes - from the widely adopted and established through to cutting-edge NGS and precision diagnostics.
About LGC
LGC, a major player in the global life science tools industry, supplies critical components in high-growth areas of human healthcare and applied markets. Its premium product lineup features essential tools for genomic analysis and quality assurance, known for their performance and quality.
Our values
- PASSION
- CURIOSITY
- INTEGRITY
- BRILLIANCE
- RESPECT
Equal opportunity, accessibility and legal noticesLGC Group's statements, word for word
Equal opportunities
LGC is committed to ensuring that every potential applicant and employee is appreciated for their distinct abilities, without any bias based on age, disability, race, ethnicity, gender, sexual orientation, gender identity, marital status, pregnancy, parenthood, religion, or beliefs. The evaluation and selection of candidates will always be conducted without taking these aspects into account.
For more information about LGC, please visit our website www.lgcgroup.com
Job intelligence
The context around this role
Live data · October 16, 2026
Salary intelligence
How the pay compares
Associate & Specialist roles in the US104 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| All US (middle half) | $49,375 | $60,000 | $76,625 |
Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, October 16, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Control
The general path across 290 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not LGC Group's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 16 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Lab testing and methods3
- Documentation and SOPs1
- Data and digital systems1
- Collaboration and leadership1
Company hiring pulse
LGC Group on Regulatory Jobs
- 2
- Open roles
- 2
- Distinct roles
- 2
- Locations
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QC Technologist I at LGC Group
Open until filled.