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ElevateBio

Specialist I, QC Logistics

Waltham, MA · On-site

$43 - $57/hr

The Role: The QC Specialist I, Logistics will support QC analytical activities outsourced to contract testing laboratories as well as QC logistics at ElevateBio. This role will require the ...

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How much do testing laboratories jobs pay per hour?

As of Jun 27, 2026, the average hourly pay for testing laboratories in the United States is $25.78, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $31.49 per hour, depending on experience, location, and employer.

What jobs in the US pay $300,000 a year?

In testing laboratories, senior roles such as Laboratory Directors, Quality Assurance Managers, or specialized senior scientists can reach or exceed $300,000 annually, especially with extensive experience, advanced certifications, and leadership responsibilities. These positions often require advanced degrees, industry expertise, and management skills, and may involve overseeing complex testing operations or regulatory compliance.

What job makes $10,000 a month without a degree?

In testing laboratories, roles such as senior laboratory technician or quality assurance manager can potentially earn around $10,000 per month with extensive experience and specialized skills. These positions often require certifications, technical expertise, and a strong understanding of testing procedures, but may not always require a formal degree.

What is the highest paying laboratory job?

In testing laboratories, senior roles such as Laboratory Directors or Quality Assurance Managers tend to have the highest salaries, often exceeding $100,000 annually. These positions typically require advanced degrees, extensive experience, and certifications like ISO or CLIA, depending on the laboratory type.

What is the difference between Testing Laboratories vs Quality Control Inspectors?

AspectTesting LaboratoriesQuality Control Inspectors
CredentialsOften require certifications like ISO/IEC 17025, technical degreesMay require high school diploma, technical training
Work EnvironmentLaboratory settings with specialized equipmentManufacturing or production sites, inspection areas
Industry UsageUsed across various industries for testing products and materialsFocus on inspecting products during or after production

Testing Laboratories perform detailed analysis and testing of materials and products in lab settings, ensuring compliance with standards. Quality Control Inspectors primarily examine products during manufacturing to identify defects. While both roles aim to ensure product quality, Testing Laboratories focus on testing and certification, whereas Quality Control Inspectors focus on inspection and defect detection during production.

Is lab technician a good career?

A lab technician is a valuable role in testing laboratories, involving tasks such as conducting experiments, analyzing samples, and maintaining equipment. The career typically requires technical skills, attention to detail, and often certification or training, with job prospects generally stable in healthcare, manufacturing, and research sectors.
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Infographic showing various Testing Laboratories job openings in the United States as of June 2026, with employment types broken down into 25% Full Time, 70% Part Time, and 5% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $53,613 per year, or $25.8 per hour.
Specialist I, QC Logistics

Specialist I, QC Logistics

ElevateBio

Waltham, MA • On-site

$43 - $57/hr

Full-time

Posted 10 days ago

Job description

ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.
The Role:
The QC Specialist I, Logistics will support QC analytical activities outsourced to contract testing laboratories as well as QC logistics at ElevateBio. This role will require the comprehension of assay protocols and review of data analysis and reports of executed testing. This role will support the review of investigation and deviation reports generated by the testing laboratories and may assist in the preparation of in-house reports associated with these events. This role will also require supporting the outsourced testing logistics such as sample submission documentation, scheduling shipments with supply chain, material pack out, and tracking samples once submitted. The QC Specialist I will assist in QC sample management, such as labeling and receipt, and inventory management within ElevateBio. The role will also require management of stability programs from writing stability protocols to trending stability data and completing final reports. The Specialist I will author and manage client documents such as, but not limited to, product sampling plans, specifications, and certificates of analysis. Additionally, this role will have regular communication with clients to support daily operations as described above.
Here's What You'll Do:
  • Review/analyze testing protocols generated by contract testing laboratories for cell and gene therapy GMP production lots including engineering and clinical material.
  • Analyze incoming data and transfer information into internal systems (e.g. LIMS and QMS).
  • Review deviations/investigations from outsourced laboratories.
  • Manage logistics of shipping activities between contract manufacturing organization, investigators, and contract testing laboratories for both routine testing and investigational work.
  • May perform optimization and troubleshooting experiments at Elevatebio laboratories.
  • Handle internal QC sample submission process which includes labeling and sample receipt.
  • Manage QC sample inventory.
  • Author and manage change controls associated with ElevateBio processes and client requested changes.
  • Writing stability protocols and managing stability testing and data review.
  • Routine client and internal cross functional communication.

Requirements:
  • Bachelor's degree in technical discipline (Biology/Chemistry/Microbiology/Engineering or related field) with a minimum of 3-5 years of experience in Quality Assurance, Quality Control, or a GMP related field within a biotechnology, biologics, or pharmaceutical manufacturing facility.
  • Experience with typical gene and cell therapy test methodologies (PCR, Flow Cytometry, ELISA/ELISpot, HPLC and cell-based assays).
  • Ability to communicate and work independently with scientific/technical personnel.
  • Strong knowledge of GMP, SOPs, and quality system processes.
  • Experience writing quality event records such as deviations, change controls, and corrective actions.
  • Excellent organizational skills.
  • Experience in cell and gene therapy manufacturing environment is a plus
  • Experience performing laboratory investigations

The budgeted range for this position is $43/hour - $57/hour. This range is a good faith estimate of the expected hourly range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law.
ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

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