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Associate Quality Control Analyst Jobs in Hanover, MA

Emergent Biosolutions

Analyst II, QC Raw Materials

Canton, MA · On-site

$25.50 - $34/hr

Represents QC in vendor relations, including contract support and working with vendors during ... Follows good laboratory practices and procedures in analyzing situations or data from which answers ...

Emergent Biosolutions

Analyst II, QC Raw Materials

Canton, MA · On-site

$25.50 - $34/hr

Represents QC in vendor relations, including contract support and working with vendors during ... Follows good laboratory practices and procedures in analyzing situations or data from which answers ...

Medium

Associate Director, Quality Control

Waltham, MA · On-site

$160 - $200/hr

We are seeking an experienced Associate Director of Quality Control (QC) to lead QC operations ... Minimum 10 years of industry experience in biologics analytical development and QC. * Deep ...

Rust-Oleum

Mgr/Quality Control

Attleboro, MA

Analyze quality control test results and provide feedback and interpretation to production ... Ability to supervise/manage diverse group of associates and managers. * Significant experience with ...

Kop-Coat, Inc.

Mgr/Quality Control

Attleboro, MA

Analyze quality control test results and provide feedback and interpretation to production ... Ability to supervise/manage diverse group of associates and managers. * Significant experience with ...

Tremco Construction

Mgr/Quality Control

Attleboro, MA · On-site

Analyze quality control test results and provide feedback and interpretation to production ... Ability to supervise/manage diverse group of associates and managers. * Significant experience with ...

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All JobsAssociate Quality Control Analyst JobsAssociate Quality Control Analyst Jobs in Hanover, MA

Associate Quality Control Analyst information

See Hanover, MA salary details

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

As of Sep 5, 2026, the average hourly pay for associate quality control analyst in Hanover, MA is $29.13, according to ZipRecruiter salary data. Most workers in this role earn between $24.09 and $32.36 per hour, depending on experience, location, and employer.

What does an associate quality control analyst do?

An Associate Quality Control Analyst is responsible for testing and inspecting products, materials, or processes to ensure they meet established quality standards. They perform routine laboratory tests, document results, and identify any deviations from specifications. These analysts often work in industries like pharmaceuticals, manufacturing, or food production, supporting senior analysts and quality managers. Their role is crucial in maintaining product safety, consistency, and regulatory compliance.

What are the key skills and qualifications needed to thrive as an associate quality control analyst?

To thrive as an Associate Quality Control Analyst, you need a solid background in biology, chemistry, or a related scientific field, often with a relevant bachelor's degree. Familiarity with laboratory equipment, quality management systems (such as LIMS), and regulatory guidelines like GMP is typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills for identifying and resolving quality issues. These skills and qualifications ensure accuracy, compliance, and consistent product quality in laboratory and manufacturing environments.

What are some common challenges faced by associate quality control analysts during routine testing, and how can they be addressed?

Associate Quality Control Analysts often encounter challenges such as tight deadlines, managing multiple sample types, and handling complex analytical instruments. Staying organized and maintaining clear documentation helps manage workflow efficiently. Regular calibration and maintenance of laboratory equipment, along with ongoing training, are essential to minimize errors and ensure accurate results. Collaborating closely with senior analysts and cross-functional teams can also help troubleshoot unexpected issues and streamline processes.

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

AspectAssociate Quality Control AnalystQuality Control Technician
CredentialsBachelor's degree in life sciences or related field; certifications like CQE are commonHigh school diploma or associate degree; technical certifications may be preferred
Work EnvironmentLaboratories, manufacturing facilities, quality assurance departmentsManufacturing sites, laboratories, production lines
Job ResponsibilitiesData analysis, documentation, reviewing quality processes, supporting auditsPerforming tests, inspecting products, recording test results

While both roles support quality assurance, the Associate Quality Control Analyst typically focuses on data analysis and documentation, whereas the Quality Control Technician primarily conducts tests and inspections. The analyst role often requires a higher level of education and analytical skills, making it suitable for those interested in quality systems and compliance.

Associate Quality Control Analyst jobs near you

Associate Director, Quality Control

Beam Therapeutics

Cambridge, MA • On-site

Full-time

Posted 8 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 to lead the Beam Massachusetts Quality Control team in delivering compliant, scientifically sound, and timely GMP testing while maintaining a continuous state of laboratory and inspection readiness. This on-site role will provide site-based QC leadership for routine GMP testing operations supporting Beam's clinical and late-stage programs, and will help support the team's transition from a clinical-stage QC group to a late-stage, commercial QC operation.
The successful candidate will be responsible for leading a team performing release, stability, method qualification/validation, and method transfer testing while ensuring that analytical methods, laboratory equipment, LIMS/LES builds, method templates, reagents, reference standards, sample workflows, documentation, training, audit trails, and data systems remain ready for GMP use and regulatory inspection. Additionally, the Associate Director will own or oversee key QC quality systems, including deviations, laboratory investigations, change controls, CAPAs, effectiveness checks, and continuous improvement initiatives.
The position will also play a critical role in supporting commercial and BLA readiness by ensuring the Massachusetts QC laboratory is prepared to support regulatory inspections, routine clinical product testing, quality-system execution, and ongoing laboratory performance improvement. The role requires a strong leader who can balance daily testing execution, compliance rigor, scientific judgment, staff development, cross-functional influence, and long-term operational readiness.
Primary Responsibilities:
  • Lead the Massachusetts QC organization to ensure timely, compliant, and scientifically sound execution of GMP testing, including release, stability, method qualification/validation, and method transfer testing.
  • Provide direct leadership and oversight for QC staff performing routine GMP testing, data review, laboratory investigations, method troubleshooting, and inspection support.
  • Ensure the QC laboratory remains in a continuous state of inspection readiness, including readiness of methods, instruments, data systems, documentation, training records, audit trails, analyst qualifications, and SME preparation.
  • Own or oversee QC quality-system records and processes, including deviations, laboratory investigations, change controls, CAPAs, effectiveness checks, and continuous improvement actions.
  • Partner with Data Integrity and Quality Systems to ensure GMP data meet ALCOA+ principles and remain complete, consistent, accurate, attributable, legible, contemporaneous, original or true copy, and secure throughout the data lifecycle.
  • Maintain analytical method and laboratory readiness by ensuring appropriate control of analytical equipment, LIMS/LES builds, method templates, reagents, reference standards, sample workflows, and supporting documentation.
  • Ensure QC testing operations are appropriately planned and resourced to support clinical manufacturing, release timelines, stability commitments, method lifecycle activities, and commercial/BLA readiness.
  • Use quality metrics, recurring deviations, invalid assay trends, audit observations, capacity constraints, and inspection-readiness commitments to drive continuous improvement and reduce compliance risk.
  • Provide leadership for laboratory issue resolution, including escalation of testing delays, equipment constraints, data integrity risks, investigation trends, method performance issues, and quality-system bottlenecks.
  • Ensure team members are trained and qualified for GMP activities, including method execution, data review, deviation support, documentation practices, inspection interactions, and applicable data integrity expectations.
  • Coach and develop QC staff, including supporting individual development plans, technical growth, career development, succession planning, and readiness for expanded responsibilities.
  • Serve as a key QC interface with QA, Manufacturing, MS&T, Analytical Research & Development, Regulatory Affairs, Supply Chain, LabOps, CSV, CQV, IT, Quality Systems, and other cross-functional partners.
  • Support preparation for regulatory inspections, mock inspections, health authority interactions, and internal/external audits by ensuring QC records, SMEs, laboratory systems, and supporting evidence are inspection-ready.
  • Provide clear communication to site and functional leadership regarding QC operational status, quality-system commitments, inspection-readiness risks, resource needs, and critical path activities.

Qualifications:
  • Advanced degree, or equivalent experience, in Chemistry, Biochemistry, Molecular Biology, Cell Biology, Analytical Sciences, Pharmaceutical Sciences, or a related scientific discipline.
  • 8+ years of relevant industry experience in Quality Control within biologics, cell therapy, gene therapy, mRNA, or other complex therapeutic modalities.
  • Prior experience leading or managing a GMP Quality Control laboratory team responsible for routine testing, data review, investigations, method execution, and inspection readiness.
  • Strong understanding of GMP laboratory operations, including release testing, stability testing, in-process testing, method qualification/validation, method transfer, sample management, equipment readiness, and laboratory documentation.
  • Demonstrated experience with quality systems, including deviations, laboratory investigations, change controls, CAPAs, effectiveness checks, root cause analysis, and continuous improvement.
  • Working knowledge of data integrity expectations, including ALCOA+ principles, audit trail review, computerized system controls, electronic records, validated spreadsheets, data lifecycle management, and inspection expectations for GMP data.
  • Experience supporting regulatory inspections, mock inspections, internal audits, or inspection-readiness remediation activities in a GMP laboratory environment.
  • Demonstrated ability to lead cross-functional issue resolution involving QC, QA, Manufacturing, MS&T, Analytical Research & Development, Regulatory Affairs, Supply Chain, LabOps, CSV, CQV, IT, and Quality Systems.
  • Strong technical judgment and problem-solving skills, with the ability to assess risk, interpret laboratory data, identify trends, support investigations, and translate findings into practical corrective and preventive actions.
  • Proven ability to manage competing priorities across routine testing, quality-system commitments, method readiness, inspection readiness, and staff development.
  • Excellent written and verbal communication skills, including the ability to clearly communicate technical, operational, and compliance topics to senior leaders, cross-functional teams, auditors, and regulatory inspectors.
  • This is an on-site role at the Beam Therapeutics Quality Control laboratory in Cambridge, MA.

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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