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Quality Control Lab Analyst Jobs in Arlington, MA

Artis BioSolutions

QC Analyst 1

Watertown, MA · On-site

$26 - $35/hr

The Quality Control - Analytics department supports a growing portfolio of cell and gene therapy ... This is a hands-on lab-based position requiring flexibility based on cell & gene therapy drug ...

Atrium

Quality Lab Technician

Boston, MA · On-site

$22 - $25/hr

Collect, analyze, and document test data accurately. * Prepare comprehensive laboratory reports ... Prior experience in a laboratory, quality control, or manufacturing inspection environment.

Replimune

Scientist I, Quality Control

Framingham, MA · On-site

$112K - $146K/yr

Responsible for change control, deviations and CAPA's related to QC Analytical operations including conducting OOS, OOT, and lab investigations. * Assist with audits and regulatory inspections, as ...

Rentschler

Quality Control Data Reviewer

Milford, MA · On-site

$90K - $110K/yr

Review and approval of cGMP analytical data comparing results to internal and customer ... Must be able to work safely in a lab environment * PPE as required Base Pay Range $90,000 - $110 ...

rentschler

Quality Control Data Reviewer

Milford, MA · On-site

$90K - $110K/yr

Review and approval of cGMP analytical data comparing results to internal and customer ... Must be able to work safely in a lab environment * PPE as required Base Pay Range $90,000 - $110 ...

Integrated Resources INC

QC Microbiologist

Andover, MA

$25.75 - $34/hr

Known lab errors investigation for root cause and impact Requirements for role will include ... cause analysis and impact analysis Experience with Trackwise/LIMS preferred Qualifications ...

Eversource Energy

Gas Quality Control Analyst

Somerville, MA · On-site

$26.25 - $35.25/hr

The QC Specialist has the authority to direct and stop, if necessary, work to ensure compliance ... Mental Aspects : * Work includes analyzing, planning, organizing, evaluating and documenting.

Eversource Energy

Gas Quality Control Analyst

Hyde Park, MA · On-site

$24.50 - $33/hr

The QC Specialist has the authority to direct and stop, if necessary, work to ensure compliance ... Mental Aspects : * Work includes analyzing, planning, organizing, evaluating and documenting.

Zifo

GxP Lab Computing Analyst

Framingham, MA · On-site

The Zifo Lab Computing Analyst provides both consulting, analytical and technical laboratory ... QC, Medical Devices, specialty chemicals and other research-based organizations. Our team ...

Pace

Sr. Quality Control Analyst

Waltham, MA · On-site

$105K - $120K/yr

Train and mentor team members on analytical methods, instrumentation, and best practices, as required * Collaborate across teams to improve efficiency and deliver high-quality results. * Promote a ...

Rentschler

Quality Control Data Reviewer

Milford, MA · Hybrid

$90K - $110K/yr

Review and approval of QC test analytics; in process, release, stability, validation Track ... Must be able to work safely in a lab environment * PPE as required _____ Base Pay Range $90,000 ...

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Showing results 21-40

All JobsQuality Control Lab Analyst JobsQuality Control Lab Analyst Jobs in Arlington, MA

Quality Control Lab Analyst information

See Arlington, MA salary details

$19

$31

$46

How much do quality control lab analyst jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for quality control lab analyst in Arlington, MA is $31.61, according to ZipRecruiter salary data. Most workers in this role earn between $26.15 and $35.10 per hour, depending on experience, location, and employer.

What is the difference between Quality Control Lab Analyst vs Quality Control Technician?

AspectQuality Control Lab AnalystQuality Control Technician
CredentialsTypically requires a degree in science or related field; certifications like ASQ or laboratory-specific training are commonOften requires a high school diploma or associate degree; some certifications may be preferred
Work EnvironmentLaboratory setting, performing tests and analyses on samplesManufacturing or production environment, performing inspections and sample collection
Industry UsageUsed across pharmaceutical, biotech, food, and chemical industriesCommon in manufacturing, food production, and pharmaceuticals

The main difference is that a Quality Control Lab Analyst typically conducts detailed laboratory testing and analysis, often requiring more specialized education and certifications. In contrast, a Quality Control Technician focuses on sample collection, inspection, and basic testing in production environments. Both roles are essential for quality assurance but differ in scope and responsibilities.

What are popular job titles related to Quality Control Lab Analyst jobs in Arlington, MA?

For Quality Control Lab Analyst jobs in Arlington, MA, the most frequently searched job titles are:

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The top searched job categories for Quality Control Lab Analyst jobs in Arlington, MA are:

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Cities near Arlington, MA with the most Quality Control Lab Analyst job openings:

Quality Control Lab Analyst jobs near you

QC Analyst 1

Artis BioSolutions

Watertown, MA • On-site

$26 - $35/hr

Full-time

Re-posted 18 days ago

Job description

The Quality Control - Analytics department supports a growing portfolio of cell and gene therapy (CGT) products, including CAR-T, iPSC, AAV, LVV and synthetic DNA products. We are immediately recruiting for a highly motivated QC Analyst I to perform laboratory testing with distinct technical but complementary focus within a fast-paced GMP environment. You will contribute to the development, qualification and execution of analytical methods supporting GMP release and characterization testing. Additionally, you will work cross-functionally with Analytical / Process Development, Manufacturing, and Quality Assurance to ensure methods meet regulatory and compendial expectations while supporting patient safety. This is an outstanding opportunity for a candidate to work under the guidance of a supervisor and mentor, manage time effectively, complete assigned analytical tasks in a cross-functional collaborative environment supporting development and cGMP manufacturing of cell and gene therapies.  

This role focuses on the development and optimization of UHPLC-based biophysical analytical methods and/or PCR-based, and related molecular methods supporting CGT safety, identity, purity, strength and quality testing, including residual impurity and compendial applications such as Mycoplasma detection.   

Scope of Responsibilities 

  • Complete required read/understand courses, bench-work training and quality-controlled cGMP documentation requirements. 

  • Execute assigned analytical test methods, with cGMP compliance, to support cell therapy manufacturing, vector manufacturing, and fill finish. 

  • Support analytical assay development ensuring they are robust enough for qualification, transition to quality control and successful implementation.  

  • Perform general laboratory tasks, including maintenance and troubleshooting of equipment. 

  • Maintain accurate and reliable records, electronic lab notebook entries, and all other pertinent documentation. 

  • Comply with all environmental health and safety standards. 

  • This is a hands-on lab-based position requiring flexibility based on cell & gene therapy drug product manufacturing schedule.  

  • UHPLC-Based Methods (Purity and Residual Analysis) 

  • Develop, optimize, and troubleshoot UHPLC-based methods (e.g., reverse phase, ion-pair, size exclusion etc.) for purity analysis of small molecules, DNA, RNA, and related CGT residuals.  

  • Apply molecular biology and biophysical characterization techniques to support method development.  

  • Support technical transfer and method qualification activities. 

  • Generate and review technical protocols, reports and GMP documentation. Troubleshoot chromatographic performance issues (e.g., peak shouldering, tailing, resolution) and propose corrective strategies. 

  • PCR-Based Methods (qPCR / dPCR/ ddPCR) 

  • Develop and optimize PCR methods applicable to CGT drug substance/drug product testing. 

  • Support compendial and non-compendial molecular testing. 

  • Support method transfer, qualification and troubleshooting activities. 

  • Generate and review technical protocols, reports and GMP-compliant documentation 

  • Proteomic and/or Cell-based Methods   

  • Contribute to assay development activities using cell-based and/or proteomics-based approaches, e.g., cell culture-based cytotoxicity assays, flow cytometry, ELISA/plate-reader-based assays as applicable to CGT QC. 

Required Experiences 

  • Hands-on operation of UHPLC instrumentation (e.g., Agilent, Water's platform) in a regulated or research setting. 

  • Working knowledge of molecular biology and/or biophysical characterization techniques applicable to DNA, RNA, or plasmid characterization. 

  • Hands-on experience with PCR platforms and related molecular assays. 

  • Working knowledge of proteomic or cell-based techniques used in CGT QC. 

  • Familiarity with compendial methods is a plus. 

Minimum Qualification 

  • QC Analyst I: Bachelors with minimum of 2 years or Masters with minimum of 1 year of relevant work experience, preferably in a cGMP biotechnology manufacturing environment, ideally with hands-on experience in cell and/or gene therapy. 

  • Demonstrate working knowledge of cGMP requirements. 

  • Ability to manage and prioritize tasks and projects, with the guidance of management. 

  • Strong verbal and written communication skills. 

  • Strong leadership skills, with an excitement to both roll up your sleeves and be a thoughtful partner. 

  • Detail-oriented with strong problem solving and troubleshooting skills. 

  • Applicants must possess valid, unrestricted work authorization and be available to commence work immediately upon offer.  

To Apply 

Please submit your resume/CV along with a brief cover letter describing your relevant experience for one or more applicable areas indicated above. Your cover letter should specifically address: 

  • Your hands-on experience with relevant technique 

  • Any additional relevant experience 

  • Your familiarity with GMP and regulatory framework applicable to CGT analytical testing.  

Landmark Bio is an Equal Opportunity, Affirmative Action employer. Minorities, women, veterans, and individuals with disabilities are encouraged to apply.  

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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