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Associate Quality Control Analyst Jobs in Hanover, MA

Socket.dev

Head of Quality Control

Watertown, MA · On-site

$232 - $285/hr

Cross‑Modality Analytical & QC Strategy * Lead QC strategy across antibodies, RNA, and conjugate modalities. * Drive modality‑specific analytical approaches including glycan profiling, potency ...

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 ...

American Society for Quality

Sr. QC Manager

Waltham, MA · On-site

$150 - $170/hr

Analyze quality, yield, reliability, complaint, nonconformance, and production output data to ... Experience linking QC trends, nonconformances, complaint investigations, and manufacturing ...

Dyne Tx

Director, Quality Control

Waltham, MA · On-site

$190 - $230/hr

The Director, Quality Control leads global Quality Control activities, including oversight of ... Leads analytical troubleshooting efforts in collaboration with contract laboratories * Ensures ...

Dyne Therapeutics

Director, Quality Control

Waltham, MA · On-site

$190K - $230K/yr

The Director, Quality Control leads global Quality Control activities, including oversight of ... Leads analytical troubleshooting efforts in collaboration with contract laboratories * Ensures ...

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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 Aug 12, 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 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.

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.
Associate Quality Control Analyst jobs near you

Director, QC Analytical

Viridian Therapeutics, Inc.

Waltham, MA • On-site

$192K - $235K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 22 days ago

Job description

Description
At Viridian, we are focused on developing best-in-class medicines for people living with autoimmune and rare diseases. Leveraging our team's expertise in antibody discovery and engineering, we have created a robust pipeline of differentiated investigational therapeutic candidates for well-validated targets.
Reporting to the Executive Director of Quality Control, the Director of QC Analytical will lead teams responsible for critical QC Analytical functions, including Method performance, method transfer, specification, Reference standard/critical reagent management, supplier oversight management of key quality systems for respective areas. This role will partner closely with internal stakeholders and external organizations to develop, implement, and continually improve operational strategies while maintaining full compliance with applicable quality and regulatory requirements.
This role is based in our Waltham, MA headquarters. Our office-based employees are required to work in the office three (3) days a week.
Responsibilities (including, but not limited to):
  • Provide strategic leadership to the QC Analytical team, including oversight of external partners to support all stages of program development
  • Collaborate closely with CMC functions, including Analytical Development and Process Development, to ensure aligned QC support
  • Lead method lifecycle management for QC owned methods including transfers, validations, performance monitoring, and improvements
  • Provide strategic oversight for late phase reference standard implementation and ongoing lifecycle management
  • Provide oversight of specifications throughout product lifecycle
  • Analyze and present data, present to both internal and external stakeholders
  • Ensure QC deliverables are met and provide leadership/professional development for team
  • Oversee external partners (e.g., CMOs, CTLs) to ensure adherence to quality and regulatory expectations
  • Support regulatory submissions by authoring and reviewing relevant CMC sections
  • Prepare QC personnel for inspection readiness, support vendor audits, and serve as the QC subject matter expert during inspections
  • Oversee quality records within assigned areas, including robust management of OOS/OOT investigations and related deliverables

Requirements
Qualifications:
  • Require a BS, MS, or PhD in a life science discipline with a 12+ years of relevant industry experience
  • Strong background in analytical methods and data analysis, including compendial methods
  • Demonstrated leadership experience in QC operations and oversight of external CMOs/CTLs
  • Deep knowledge of cGMP, ICH, FDA, and EU regulations and guidance
  • Proven hands-on experience with analytical methods including but not limited to SEC, icIEF, CE-SDS, Peptide mapping, Potency and compendial methods as well as functional device testing
  • Strong people leadership skills, with experience coaching, developing, and managing staff at various levels
  • Comfortable in an adaptable small company environment with minimal direction and able to adjust workload based upon changing priorities
  • Strong commitment to ethical standards
  • Proficient with Microsoft Office suite (i.e., Word, PowerPoint, Excel, Outlook, SharePoint, etc.)
  • Ability to travel up to 5%
  • The salary range for this position is commensurate with experience

Viridian offers a comprehensive benefits package including:
• Competitive pay and stock options for all employees
• Medical, dental, and vision insurance
• 100% Paid Parental Leave
• Short- and long-term disability coverage
• Life, Travel and AD&D
• 401(k) Company Match with immediate company vest
• Employee Stock Purchase plan
• Generous vacation plan and paid company holiday shutdowns
• Various fertility, mental, financial, and proactive physical health programs
Viridian Therapeutics, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination, harassment, or retaliation of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by Federal, State, and Local laws. Viridian will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Viridian Therapeutics, Inc participates in E-Verify, the federal program for electronic verification of employment eligibility.

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