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Associate Director Quality Control Jobs in Boston, MA

Editas Medicine

Director, Quality Control

Cambridge, MA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

As the Director, Quality Control, you will: * Lead phase appropriate CMC analytical development, qualification/validation, transfer and optimization through strong collaboration with key stakeholders ...

Editas Medicine

Director, Quality Control

Cambridge, MA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

As the Director, Quality Control, you will: * Lead phase appropriate CMC analytical development, qualification/validation, transfer and optimization through strong collaboration with key stakeholders ...

Viridian Therapeutics, Inc.

Director, QC Analytical

Waltham, MA · On-site

$192K - $235K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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 ...

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 Quality Control activities supporting the development, manufacture, testing, release, and lifecycle ...

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 Quality Control activities supporting the development, manufacture, testing, release, and lifecycle ...

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All JobsAssociate Quality Control JobsAssociate Director Quality Control JobsAssociate Director Quality Control Jobs in Boston, MA

Associate Director Quality Control information

See Boston, MA salary details

$33.7K

$136.5K

$231.9K

How much do associate director quality control jobs pay per year?

As of Aug 19, 2026, the average yearly pay for associate director quality control in Boston, MA is $136,453.00, according to ZipRecruiter salary data. Most workers in this role earn between $98,900.00 and $164,000.00 per year, depending on experience, location, and employer.

What is an associate director quality control?

An Associate Director of Quality Control is a senior management professional responsible for overseeing the quality control processes within an organization, often in industries like pharmaceuticals, biotechnology, or manufacturing. They lead teams that test and monitor product quality, ensure compliance with regulatory standards, and develop strategies to improve testing procedures. Their role involves managing budgets, mentoring staff, and collaborating with other departments to uphold product integrity. Associate Directors of Quality Control often report to higher-level executives and play a key role in maintaining customer trust and regulatory approval.

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

To thrive as an Associate Director of Quality Control, you need in-depth knowledge of quality management systems, regulatory compliance, and relevant scientific or technical expertise, typically supported by a degree in life sciences or engineering. Familiarity with laboratory information management systems (LIMS), quality assurance software, and certifications such as Six Sigma or ASQ are highly valuable. Leadership, problem-solving, and strong communication skills help drive team performance and foster cross-functional collaboration. These skills ensure rigorous product quality, regulatory adherence, and operational efficiency in quality-driven environments.

What are the main challenges an associate director quality control typically faces when managing a diverse QC team?

An Associate Director of Quality Control often manages teams with varied technical backgrounds, which can lead to challenges in aligning processes, maintaining consistent training standards, and ensuring clear communication across functions. Balancing the demands of regulatory compliance, tight production timelines, and continuous improvement initiatives is also a common challenge. Successful leaders in this role foster a culture of collaboration, prioritize ongoing training, and implement standardized procedures to help their teams deliver reliable results and support broader organizational goals.

What is the difference between Associate Director Quality Control vs Quality Control Manager?

AspectAssociate Director Quality ControlQuality Control Manager
CredentialsBachelor's/Master's in Life Sciences, Quality Certifications (e.g., CQE)Bachelor's/Master's in Life Sciences, Quality Certifications (e.g., CQE)
Work EnvironmentLeadership role in labs or manufacturing facilities, overseeing teamsSupervises QC teams, conducts testing, and ensures compliance
Industry UsageUsed in pharmaceutical, biotech, and biotech manufacturing companiesCommon in similar industries, often reporting to Associate Directors

The Associate Director Quality Control typically holds a higher strategic and leadership role, overseeing multiple teams and ensuring compliance at a broader level. The Quality Control Manager focuses more on daily testing, team supervision, and operational tasks. Both roles require similar credentials but differ in scope and responsibility.

What are popular job titles related to Associate Director Quality Control jobs in Boston, MA?

For Associate Director Quality Control jobs in Boston, MA, the most frequently searched job titles are:

What job categories do people searching Associate Director Quality Control jobs in Boston, MA look for?

The top searched job categories for Associate Director Quality Control jobs in Boston, MA are:

What cities near Boston, MA are hiring for Associate Director Quality Control jobs?

Cities near Boston, MA with the most Associate Director Quality Control job openings:

Associate Director Quality Control jobs near you
Infographic showing various Associate Director Quality Control job openings in Boston, MA as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 13% Part Time, 5% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $136,453 per year, or $65.6 per hour.

Director, Quality Control

Editas Medicine

Cambridge, MA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 3 days ago

Job description

At Editas Medicine, we are pioneering the possible. Our mission and commitment is to translate the power and potential of the CRISPR/Cas12a and CRISPR/Cas9 genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for a broad class of diseases.
Why Choose Editas?
At Editas Medicine, we're a team of courageous problem solvers, harnessing the power and potential of CRISPR gene editing to transform the future of medicine. Driven by a shared purpose to serve people living with serious diseases, we succeed together through collaboration, mutual respect, and innovation. If you want to be part of a team where your voice is heard and respected, where you can operate at the forefront of gene editing, and push the boundaries of what's possible in medicine, come join us and become an Editor!
Decoding The Role:
The Quality team is seeking a highly motivated and experienced technical and organizational leader in gRNA, mRNA, and Lipid Nanoparticle (LNP) analytical methodologies and GMP testing. The successful candidate will collaborate with a high-performing CMC team, coordinating with process and analytical experts cross-functionally in Research and Discovery, Process Development, Analytical Sciences, Manufacturing, and Quality Assurance, to transfer, qualify and oversee in-process and release testing to advance Editas' in vivo gene medicine portfolio. The individual will also be a key contributor to the overall program CMC strategy. This role requires strong analytical expertise, GMP experience, as well as a passion to lead, mentor and influence people.
Characterizing Your Impact:
As the Director, Quality Control, you will:
  • Lead phase appropriate CMC analytical development, qualification/validation, transfer and optimization through strong collaboration with key stakeholders and external partners.
  • Drive the analytical control strategy for in vivo medicines towards IND/CTA and clinical manufacturing.
  • Ensure seamless transition of analytics from Analytical Sciences and into GMP manufacturing.
  • Collaborate with QA to generate, review and approve documentation, including: SOPs, change controls, deviations, CAPAs and OOS/OOT investigation reports.
  • Act as the lead Subject Matter Expert for gRNA, mRNA, and drug delivery (e.g., LNP) control strategy to direct the.
  • Establish phase-appropriate specifications based on sound scientific rationale for critical starting materials (e.g. pDNA), drug substance (e.g. gRNA and mRNA), excipients (e.g. lipids and targeting moieties), and drug product (e.g. LNP).
  • Oversee the external GMP testing of critical starting materials, novel excipients, drug substance and drug product for clinical use.
  • Implement stability programs to establish the retest dates/shelf life of critical starting materials, novel excipients, drug substance and drug product for clinical use.
  • Lead cross-functional projects/working teams, champion new ideas/business process improvements to advance company's in vivo pipeline and technology platforms.
  • Author and review of regulatory submissions, technical reports, SOPs and work instructions.
  • Stay up to date with the latest industry trends and product knowledge.
  • Work cross-functionally (e.g. with Research, Business Development and Legal) to evaluate novel manufacturing technologies and new business partners.

Requirements
The Ideal Transcript:
To thrive in this role, you'll need:
  • Degree in Microbiology, Biomedical Engineering, Chemistry, Pharmaceutical Sciences, or related discipline with 8+ (Ph.D.), 10+ (M.S.), 12+ (B.S.) years of relevant experience in drug development.
  • Strong technical expertise and hands-on experience with analytical test method optimization, validation, and transfers as well as CTO/CMO management are required.
  • In-depth expertise in critical raw material, drug substance, and drug product characterization methods and specifications are highly desirable.
  • Ability to develop analytical control strategies that are phase-appropriate (i.e., phase 1 vs. phase 3 requirements) and grounded in principles of risk management.
  • Ability to apply Quality-by-Design (QbD) principles to process development strategy planning and execution is required.
  • Exceptional leadership and interpersonal skills as well as excellent presentation and scientific/technical writing skills is a must.
  • Strong organizational skills, and ability to multi-task, problem-solve, and adjust priorities to meet goals in a fast-paced environment.
  • Experience in leading cross-functional collaborations with other internal departments as well as external CDMOs.
  • Understanding related industry guidance's (FDA, PDA, ICH and BPOG), knowledge of FDA, EMA and ICH regulations, and understanding of product development life cycle.

Benefits
Editas provides a comprehensive array of benefits to all employees, including a Blue Cross Blue Shield PPO Medical Plan, a company-funded Health Savings Account, Dental and Vision Insurance, Life and Disability Insurance, Dependent Care Account, Tuition Reimbursement, 401(k) plan with company match, Employee Assistance Plan, Wellness Programs, and a flexible Paid Time Off policy.
Salary Range:
$215,000 - $235,000
Pay Transparency
Editas Medicine is committed to transparency and accuracy in our hiring practices. The anticipated salary range for each position is posted within the role. The final salary offer will be determined based on a comprehensive assessment of the candidate's qualifications, including education, training, and relevant experience. Additional factors such as external market conditions, the role's criticality, and internal equity will also be considered. Editas Medicine's compensation philosophy ensures fair and equitable pay practices.
Aspire to be an Editor? We invite you to apply and join us at the forefront of innovation and be a key contributor to realizing Editas Medicine's mission of developing transformative medicines for people living with serious diseases.

Apply