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Quality Control Associate Jobs in Boston, MA (NOW HIRING)

Amrize

Quality Control Technician II

Saugus, MA

$19 - $24.50/hr

Provides QC support on various residential and commercial projects WHAT YOU'LL ACCOMPLISH ... Associate's degree Required Work Experience: 3-5 year Required Training/Certifications: State ...

Amrize

Quality Control Technician II

Saugus, MA

$19 - $24.50/hr

Provides QC support on various residential and commercial projects WHAT YOU'LL ACCOMPLISH ... Associate's degree Required Work Experience: 3-5 year Required Training/Certifications: State ...

Amrize

Quality Control Technician II

Saugus, MA · On-site

$19 - $24.50/hr

Provides QC support on various residential and commercial projects WHAT YOU'LL ACCOMPLISH ... Associate's degree Required Work Experience: 3-5 year Required Training/Certifications: State ...

Amrize

Quality Control Technician II 1

Wrentham, MA

$20.50 - $26.25/hr

We're seeking a Quality Control Technician II who's ready to put your skills to work on projects ... Associate's degree Required Work Experience: 3-5 year Required Training/Certifications: State ...

Kelly Services

QC Analytical Technician

Wilmington, MA · On-site

$25 - $27/hr

Kelly Science & Clinical is seeking a QC Analytical Lab Technician near Wilmington, MA. Contract ... Associate or Bachelor's degree in Chemistry or related science field preferred. * 0-3 years of ...

Amrize

Quality Control Technician II 1

Wrentham, MA

$20.50 - $26.25/hr

Provides QC support on various residential and commercial projects WHAT YOU'LL ACCOMPLISH ... Associate's degree Required Work Experience: 3-5 year Required Training/Certifications: State ...

Kelly Services

QC Analytical Technician

Wilmington, MA

$25 - $27/hr

Kelly Science & Clinical is seeking a QC Analytical Lab Technician near Wilmington, MA. Contract ... Associate or Bachelor's degree in Chemistry or related science field preferred. * 0-3 years of ...

Amrize

Quality Control Technician II 1

Wrentham, MA · On-site

$20.50 - $26.25/hr

Provides QC support on various residential and commercial projects WHAT YOU'LL ACCOMPLISH ... Associate's degree Required Work Experience: 3-5 year Required Training/Certifications: State ...

Amrize

Quality Control Technician II 1

Wrentham, MA

$20.50 - $26.25/hr

Provides QC support on various residential and commercial projects WHAT YOU'LL ACCOMPLISH ... Associate's degree Required Work Experience: 3-5 year Required Training/Certifications: State ...

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All JobsQuality Control Associate JobsQuality Control Associate Jobs in Boston, MA

Quality Control Associate information

See Boston, MA salary details

$12

$27

$41

How much do quality control associate jobs pay per hour?

As of Jul 16, 2026, the average hourly pay for quality control associate in Boston, MA is $27.66, according to ZipRecruiter salary data. Most workers in this role earn between $20.10 and $33.70 per hour, depending on experience, location, and employer.

What is a QC Associate job description?

A Quality Control (QC) Associate is responsible for inspecting and testing products or materials to ensure they meet quality standards and specifications. They document findings, identify defects, and collaborate with production teams to address issues, often using tools like measurement instruments and quality management systems. The role typically requires attention to detail, knowledge of quality procedures, and adherence to safety protocols.

What does a Quality Control Associate do?

A Quality Control Associate is responsible for ensuring that products meet established standards of quality, including reliability, usability, and performance. They conduct inspections, perform tests, and document their findings to identify defects or deviations from specifications. Quality Control Associates often work closely with production teams to address issues and help maintain compliance with industry regulations. Their role is critical in maintaining customer satisfaction and upholding the reputation of their company. They may work in a variety of industries, including pharmaceuticals, manufacturing, and food production.

What are the key skills and qualifications needed to thrive as a Quality Control Associate, and why are they important?

To thrive as a Quality Control Associate, you need a solid understanding of quality assurance principles, attention to detail, and often a background in science or manufacturing. Familiarity with inspection tools, laboratory equipment, and quality management systems (such as ISO standards) is typically required, and certifications like Six Sigma or ASQ may be advantageous. Strong analytical thinking, problem-solving abilities, and effective communication skills set exceptional candidates apart. These skills ensure that products consistently meet standards, reduce errors, and support overall operational excellence.

What are some common challenges Quality Control Associates face when ensuring product consistency across different production batches?

Quality Control Associates often encounter challenges such as variations in raw material quality, changes in manufacturing processes, and tight production schedules that can lead to inconsistencies between batches. Addressing these issues requires keen attention to detail, effective communication with production teams, and a strong understanding of standard operating procedures. Staying proactive in identifying potential sources of variation and collaborating closely with other departments helps maintain high product standards and minimizes the risk of defects.

Which pays more, QA or QC?

Quality Assurance (QA) and Quality Control (QC) roles often have similar pay scales, but QA positions typically offer higher salaries due to their focus on process improvement and prevention. Factors such as industry, experience, certifications, and location can influence compensation for both roles.

What do quality control associates do?

Quality control associates inspect products, materials, or processes to ensure they meet quality standards and specifications. They perform tests, document findings, and may use tools like calipers or microscopes, often working in manufacturing or production environments to identify defects and ensure product consistency.

What is the difference between Quality Control Associate vs Quality Assurance Technician?

AspectQuality Control AssociateQuality Assurance Technician
CertificationsOften requires GMP, ISO, or industry-specific quality certificationsSimilar certifications, with focus on quality standards and compliance
Work EnvironmentLaboratory, manufacturing, or production settingsLaboratory, manufacturing, or quality compliance environments
Primary FocusInspecting products, testing samples, identifying defectsDeveloping and implementing quality systems, audits, and process improvements
Employer & Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, pharmaceuticals, food industry

While both roles focus on quality, the Quality Control Associate primarily inspects and tests products to identify defects, whereas the Quality Assurance Technician develops and maintains quality systems to prevent issues. Both roles are essential in ensuring product quality and compliance within manufacturing and production environments.

Is QC a high paying job?

The salary for a Quality Control Associate varies depending on industry, experience, and location, but it is generally considered an entry-level to mid-level position with moderate pay. Higher salaries are often associated with advanced certifications, specialized skills, or supervisory roles within quality control departments.
What are the most commonly searched types of Quality Control jobs in Boston, MA? The most popular types of Quality Control jobs in Boston, MA are:
What are popular job titles related to Quality Control Associate jobs in Boston, MA? For Quality Control Associate jobs in Boston, MA, the most frequently searched job titles are:
What job categories do people searching Quality Control Associate jobs in Boston, MA look for? The top searched job categories for Quality Control Associate jobs in Boston, MA are:
What cities near Boston, MA are hiring for Quality Control Associate jobs? Cities near Boston, MA with the most Quality Control Associate job openings:
Quality Control Associate jobs near you
Infographic showing various Quality Control Associate job openings in Boston, MA as of July 2026, with employment types broken down into 1% As Needed, 66% Full Time, 31% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $57,535 per year, or $27.7 per hour.
Associate Director, Quality Control Technical Services

Associate Director, Quality Control Technical Services

Beam Therapeutics

Cambridge, MA • On-site

Full-time

Re-posted 5 days ago

Job description

Company Overview:
Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.
Position Overview:
We are seeking an Associate Director, Quality Control Technical Services to lead QC CMC strategy for our ex vivo cell therapy franchise, spanning late-stage development, initial commercial launch, and ongoing lifecycle management. This role will also play a critical leadership role in defining and executing the strategy for mRNA drug substance and critical materials platforming, supporting both current programs and future pipeline scalability.
The successful candidate will work cross-functionally with Analytical Research & Development, Bioprocess Development, Manufacturing Technical Services, Manufacturing Operations, Regulatory Affairs, and Quality Assurance to drive the transfer, qualification, validation, and lifecycle management of analytical methods for gene-edited cell therapy products and associated critical materials (e.g., mRNA). These efforts will ensure analytical readiness to support regulatory submissions, agency approvals, and commercial supply.
This role will be instrumental in defining the QC testing and technical transfer strategy for next-generation autologous cell therapy manufacturing, including the transfer of automated and validated analytical methods to Beam's internal manufacturing facility. A key focus will be the internalization of validated mRNA methods into the North Carolina Quality Control laboratory, strengthening in-house testing capabilities and long-term operational resilience.
In addition, this position will contribute directly to regulatory filings, including specifications, analytical method validation reports, and CMC documentation, and will serve as a QC technical subject matter expert across program teams to ensure compliant, robust, and phase-appropriate analytical strategies.
Primary Responsibilities:
  • Lead and influence QC CMC strategy in partnership with cross-functional CMC teams for master cell banks (MCBs), plasmids, and mRNA drug substance and critical materials, supporting both ex vivo and in vivo therapy programs across development and commercialization.
  • Define and execute the QC testing, method strategy, and technical execution to enable next-generation autologous cell therapy manufacturing processes, including analytical readiness for process validation, comparability, and technology transfer.
  • Own and coordinate analytical method transfer, qualification, and validation activities across internal and external QC laboratories, ensuring compliant, phase-appropriate, and inspection-ready execution.
  • Establish and maintain analytical control strategies by tracking and trending in-process, release, and stability data, collaborating with statisticians and program teams to define and justify specifications for MCBs, plasmids, mRNA, and autologous cell therapy products.
  • Define and oversee stability strategies and programs for MCBs, plasmids, mRNA, and ex vivo cell therapy products, ensuring alignment with regulatory expectations and lifecycle needs.
  • Lead analytical method lifecycle management for late-stage and commercial ex vivo portfolio, including method performance monitoring, remediation, comparability activities, and continuous improvement.
  • Drive the internalization of validated mRNA analytical methods into Beam's North Carolina Quality Control laboratory, strengthening internal capabilities and supporting long-term commercial supply.
  • Author and review Quality System documentation, including SOPs, Change Controls, and CAPAs, to support method implementation, lifecycle changes, and inspection readiness.
  • Partner with Regulatory Affairs-CMC to author, review, and coordinate CMC sections of regulatory submissions, including specifications, method validation reports, and responses to agency queries.
  • Ensure QC visibility and alignment on regulatory interactions, including tracking agency questions, commitments, post-approval requirements, and method introduction or change strategies.
  • Serve as a key QC technical interface across CMC, Quality, Regulatory, Manufacturing, Process Development, Analytical Research & Development, and external partners, providing clear guidance, alignment, and issue resolution to advance program milestones.

Qualifications:
  • Advanced degree (MS, Ph.D) in Chemistry, Biochemistry, Molecular Biology, or a related scientific discipline, with 8+ years of relevant industry experience in Quality Control, Analytical Development, or CMC within biologics, cell therapy, or gene therapy.
  • Extensive hands-on experience with ex vivo autologous cell therapies, including CD34+ cell-based products, across late-stage development, validation, and/or commercial readiness.
  • Demonstrated technical expertise in cell handling and testing methodologies, including functional and potency assays, flow cytometry, NGS-based assays, and separation sciences. Experience with analytical method automation, qualification, and validation is strongly preferred.
  • Proven understanding of analytical method lifecycle management, including method transfer, qualification, validation, performance monitoring, remediation, and comparability, particularly for late-stage and commercial products.
  • Strong working knowledge of US and EU regulatory expectations (e.g., FDA/CBER, EMA, ICH, USP) applicable to cell and gene therapy CMC, with the ability to apply guidance in a phase-appropriate and inspection-ready manner.
  • Direct experience supporting regulatory submissions (INDs, BLAs, amendments, post-approval changes) for cell and gene therapy products, including specifications, method validation reports, and responses to health authority questions.
  • Demonstrated ability to lead and influence cross-functional program teams, partnering effectively with CMC, Manufacturing, Analytical R&D, Quality Assurance, and Regulatory Affairs in a fast-paced, matrixed environment.
  • Strong communication and leadership skills, with a track record of clearly articulating technical strategies, aligning stakeholders, and driving decisions across functions and with external partners.
  • Documented success in driving complex, program-critical initiatives to completion on time and within budget, including managing dependencies, risks, and priorities across multiple workstreams.
  • Highly developed organizational, analytical, and problem-solving skills, with the ability to interpret complex datasets, assess risk, and translate data into actionable QC and CMC strategies.

The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.
Beam Pay Range
$185,000-$225,000 USD

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