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Director Qa Testing Jobs in Boston, MA (NOW HIRING)

RPMGlobal

Director, Quality Assurance

Lexington, MA · On-site

$170 - $218/hr

The Role The Director of Quality Assurance will oversee GMP QA operations for internal ... testing records, and disposition onsite and CMO manufactured drug product to support clinical ...

Palco

QUALITY ASSURANCE TESTER II

Boston, MA · On-site

QUALITY ASSURANCE TESTER II We're Palco. We provide the management, support, and systems behind self-directed programs--the services that help people hire, pay, and manage their own caregivers with ...

Dyne Therapeutics

Director, QA GMP Operations

Waltham, MA · On-site

$188K - $230K/yr

The Director of QA GMP Operations is responsible for management of GMP quality within our external ... Change management to ensure proper evaluation of manufacturing and testing related changes by ...

Intellia Therapeutics

Director, QA for QC

Cambridge, MA · On-site

The Director, QA for QC is responsible for providing strategic and operational quality oversight of ... Ensure outsourced testing operations operate in compliance with applicable global regulations (FDA ...

Intellia Therapeutics

Director, QA for QC

Cambridge, MA · On-site

The Director, QA for QC is responsible for providing strategic and operational quality oversight of ... Ensure outsourced testing operations operate in compliance with applicable global regulations (FDA ...

SMART TECH SKILLS LLC

QA Analyst

Boston, MA · On-site

Key Responsibilities Quality Assurance & Testing * Develop, execute, and maintain test plans, test cases, and test scripts. * Perform functional, regression, integration, system, and user acceptance ...

New

Dyne Tx

Director, QA GMP Operations (Waltham)

Waltham, MA · On-site

$188K - $230K/yr

Role Summary The Director of QA GMPOperations is responsible for management of GMP quality within ... Change management to ensure proper evaluation of manufacturing and testing related changes by ...

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Director Qa Testing information

See Boston, MA salary details

$61.4K

$152.2K

$247.2K

How much do director qa testing jobs pay per year?

As of Aug 21, 2026, the average yearly pay for director qa testing in Boston, MA is $152,186.00, according to ZipRecruiter salary data. Most workers in this role earn between $111,900.00 and $183,600.00 per year, depending on experience, location, and employer.

What is a director QA testing?

A Director of QA Testing is a senior leadership role responsible for overseeing the quality assurance and testing processes within a company. They develop testing strategies, implement best practices, and lead teams to ensure software products meet quality standards. Their responsibilities include managing testing frameworks, coordinating with development teams, and ensuring compliance with regulatory requirements. They also analyze test data, drive process improvements, and align QA goals with business objectives. This role requires strong leadership, technical expertise, and a deep understanding of software testing methodologies.

What are the key skills and qualifications needed to thrive in the director QA testing position, and why are they important?

To thrive as a Director QA Testing, you need extensive experience in software quality assurance, strong leadership skills, and a deep understanding of testing methodologies and best practices, typically supported by a degree in computer science or a related field. Familiarity with industry-standard QA tools, automation frameworks, and certifications such as ISTQB are highly beneficial. Exceptional communication, problem-solving, and team management skills help you foster high performance and cross-functional collaboration. These abilities are crucial for ensuring software quality, meeting project deadlines, and driving organizational improvements.

What types of teams and stakeholders does a director QA testing typically interact with on a regular basis?

A Director QA Testing regularly collaborates with software development teams, product managers, project managers, and IT support to ensure testing processes align with project goals. They also communicate with executive leadership to report on quality metrics and quality improvement initiatives. This role often involves leading and mentoring QA engineers while coordinating test strategies with DevOps, security, and user experience teams. Effective collaboration across these groups is essential to deliver high-quality products, address issues promptly, and continuously enhance testing standards.

What are popular job titles related to Director Qa Testing jobs in Boston, MA?

For Director Qa Testing jobs in Boston, MA, the most frequently searched job titles are:

What job categories do people searching Director Qa Testing jobs in Boston, MA look for?

The top searched job categories for Director Qa Testing jobs in Boston, MA are:

Director Qa Testing jobs near you
Infographic showing various Director Qa Testing job openings in Boston, MA as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 11% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $152,186 per year, or $73.2 per hour.

Director, Quality Assurance

Agenus, Inc.

Lexington, MA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 19 days ago

Job description

We are a dedicated group of scientists, physicians, and businesspeople working together toward one goal: to discover and develop therapies that can unleash the power of the body's immune system to treat and potentially cure cancer. We are passionate about the work we do every day at Agenus to deliver on the promise of immuno-oncology. If you're looking for an inspired environment, passionate colleagues, and a culture that nurtures learning, innovation and team success, we invite you to join us.
The Role
The Director of Quality Assurance will oversee GMP QA operations for internal manufacturing and external manufacturing at CDMOs to support both Agenus and MiNK businesses. The operational role includes oversight of quality management systems & compliance, procedures, lot disposition, quality agreements, vendor management, complaints/excursions, audits, validation projects and contribute to regulatory submissions. This role will also support clinical compliance to GCPs and Inspection Readiness in collaboration with Agenus Clinical Development leadership.
This role is required to be onsite in Lexington, MA.
In the role you will:
  • Support batch record and SOP/Method development, review quality systems and associated executed batch records and testing records, and disposition onsite and CMO manufactured drug product to support clinical demand.
  • Establish, maintain and develop quality procedures to support in-house operations.
  • Review stability protocols and results, excursions, complaints and ensure timely response.
  • Lead the development, implementation, and continuous improvement of our GMP, GCP, and GLP quality systems to support clinical and commercial programs.
  • Oversee FDA, EMA, and other global regulatory inspections, ensuring readiness and successful outcomes. Lead inspection readiness activities, host regulatory inspections, and ensure timely resolution of inspection observations and commitments.
  • Partner with Manufacturing, Quality Control, Clinical Operations, Regulatory Affairs, and R&D teams to ensure quality is integrated into every stage of product development.
  • Direct vendor and contract manufacturing organization (CMO) quality oversight, including audits, quality agreements, vendor change and performance monitoring. Oversee supplier qualification activities, negotiate and maintain Quality Agreements, and ensure ongoing compliance with external manufacturing and testing partners.
  • Drive risk management initiatives, CAPA programs, and deviation investigations to ensure timely resolution and prevention of recurrence. Oversee execution of Quality Systems including Change Control, Deviations, CAPA, Risk Assessments, Complaint Investigations, Out of Specification Investigations and Product Disposition activities.
  • Support validation activities including equipment qualification, process validation, analytical method validation, technology transfer, and associated quality oversight.
  • Support Quality contributions to IND, BLA, and other global regulatory submissions as needed.
  • Lead, mentor, and inspire a high-performing team, fostering professional growth and a culture of accountability.
  • Stay ahead of evolving regulatory requirements and industry best practices, translating them into actionable strategies for the company.

Qualifications: About You
  • Bachelor's degree in a scientific discipline required; advanced degree preferred.
  • 10+ years of progressive Quality Assurance experience within the biotechnology or pharmaceutical industry, including leadership responsibilities.
  • Experience supporting biologics, cell therapy, and/or advanced therapy medicinal products (ATMPs) preferred.
  • Strong working knowledge of GMP regulations with demonstrated knowledge of FDA, EMA, ICH, and applicable global GMP, GCP, and GLP regulations.
  • Strong working knowledge of GMP manufacturing operations supporting biologics and/or cell therapy products.
  • Experience managing quality oversight of Contract Manufacturing Organizations (CMOs), contract testing laboratories, and external vendors, including supplier qualification, audits, and Quality Agreements.
  • Demonstrated experience leading or supporting FDA and international regulatory inspections and maintaining inspection readiness.
  • Experience supporting equipment qualification, process validation, analytical method validation, and technology transfer activities preferred.
  • Experience supporting quality activities across the product lifecycle, from early development through commercialization.
  • Demonstrated experience with CAPA, deviation investigations, change control, risk management, and continuous improvement initiatives.
  • Excellent written, verbal, and interpersonal communication skills with the ability to influence cross-functional teams and senior leadership.
  • Demonstrated ability to lead cross-functional teams, build collaborative partnerships across Manufacturing, Quality Control. Clinical Operations, Regulatory Affairs, and R&D, and drive quality initiatives in a fast-paced environment.
  • Strong organizational skills with the ability to prioritize multiple projects while maintaining attention to detail.
  • Ability to work independently, exercise sound judgment, and thrive in a dynamic, evolving biotechnology environment.

The targeted salary range for this position is $170,000 - $218,000 per year. Agenus is making a good faith effort to be transparent and accurate around our hiring ranges. The salary offered is commensurate with Agenus's compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, critical needs of the role, and internal equity.
#LI-JW1 #LI-Onsite
Learn More About Agenus
Explore our innovative pipeline and connect with us on LinkedIn
Why You'll Love Working at Agenus
We're proud to offer a comprehensive and inclusive benefits program designed to support your well-being, growth, and life outside of work:
  • Medical, Dental & Vision Coverage - Competitive options for both US & UK employees
  • Flexible Spending Accounts - For healthcare and dependent care expenses (US)
  • Flexible Vacation Plan - We believe time away leads to better thinking and innovation.
  • Care.com Memberships - Support for family care (US)
  • Education Assistance Program - Invest in your learning and development (US)
  • 401(k) Match
  • Employee Stock Purchase Plan
  • Employee Assistance Program (EAP) - Resources for mental health, well-being, and life support
  • Reward & Recognition Program - Celebrate contributions that move the mission forward

What We Believe
  • Patients First. We're here to make a difference-for every cancer patient.
  • Bold & United. Big goals require strong teams.
  • Integrity Always. Respect and honesty guide everything we do.
  • Own It. We take responsibility-for results and how we achieve them.
  • Always Learning. Curiosity drives innovation.
  • Bring Your Best. Every day matters.

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