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

Dyne Tx

Director, Quality Control

Waltham, MA · On-site

$190 - $230/hr

The Director, Quality Control leads global Quality Control activities, including oversight of external laboratories supporting analytical testing, release, and stability programs across clinical and ...

Dyne Therapeutics

Director, Quality Control

Waltham, MA · On-site

The Director, Quality Control leads global Quality Control activities, including oversight of external laboratories supporting analytical testing, release, and stability programs across clinical and ...

TScan Therapeutics

Director, Quality Control

Waltham, MA · On-site

$210 - $220/hr

We are seeking an experienced professional to serve as Director of QC, supporting release, characterization, and environmental monitoring (EM) testing for cellular drug products manufactured ...

Sebela Pharma

Director, Quality Control

Holbrook, MA · On-site

$150K - $190K/yr

Direct all QC laboratory activities, in support of GMP Testing, release, and stability programs, including laboratory safety, testing operations, resource allocation, and performance management.

Editas Medicine

Director, Quality Control

Cambridge, MA · On-site

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

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

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 across the company's biologics pipeline. You will report directly to the head of QC and will serve as ...

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Director Quality Control information

See Boston, MA salary details

$33.7K

$136.5K

$231.9K

How much do director quality control jobs pay per year?

As of Aug 24, 2026, the average yearly pay for 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 are some common challenges faced by a director quality control, and how can they be addressed?

Directors of Quality Control often encounter challenges such as maintaining compliance with evolving regulatory standards, managing cross-functional teams, and ensuring consistent product quality across multiple locations. To address these challenges, it's important to stay updated on industry regulations, foster open communication between departments, and implement robust training and quality management systems. Regular audits, data-driven decision making, and strong leadership are also key to overcoming obstacles and ensuring continuous improvement within quality control operations.

What are the key skills and qualifications needed to thrive as a director quality control, and why are they important?

To thrive as a Director of Quality Control, you need deep expertise in quality assurance methodologies, regulatory compliance, and management, typically supported by a degree in science or engineering and substantial industry experience. Familiarity with quality management systems (QMS) like ISO 9001, Six Sigma certification, and proficiency in data analysis tools are often required. Strong leadership, problem-solving abilities, and effective communication skills help drive cross-functional collaboration and continuous improvement. These competencies ensure product quality, regulatory adherence, and operational excellence in highly regulated industries.

Is director quality control a good career path?

A career as a Director of Quality Control is considered stable and rewarding in industries such as manufacturing, pharmaceuticals, and food production. It involves overseeing quality assurance processes, managing teams, and ensuring compliance with industry standards, often requiring strong leadership, analytical skills, and relevant certifications. The role offers opportunities for advancement and increased responsibility with experience.

What does a director of quality control do?

A director of quality control oversees the quality assurance processes within an organization, ensuring products or services meet company standards and regulatory requirements. They develop quality policies, lead testing and inspection activities, analyze data to identify issues, and coordinate with other departments to improve quality systems. Strong leadership, analytical skills, and knowledge of industry standards are essential for this role.

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

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

Director Quality Control jobs near you
Infographic showing various Director Quality Control job openings in Boston, MA as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, 4% Contract, and 1% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $136,453 per year, or $65.6 per hour.

Director, Quality Control

Dyne Therapeutics

Waltham, MA

Full-time

Re-posted 18 days ago

Job description

Role Summary:

The Director, Quality Control leads global Quality Control activities, including oversight of external laboratories supporting analytical testing, release, and stability programs across clinical and commercial stages. Provides strategic direction and operational leadership to ensure compliant, efficient, and high-quality execution of QC activities from early development through BLA and commercialization. Drives cross-functional alignment and external partnership performance while shaping the QC function to meet evolving organizational and regulatory requirements. 

This is an onsite role based in Waltham, MA.

Primary Responsibilities Include: 

Quality Control Strategy & Functional Leadership
  • Defines and executes the strategic vision for the Quality Control function to support clinical and commercial programs
  • Establishes organizational structure, capabilities, and processes to support growth and future commercialization
  • Participates in Pharmaceutical Quality leadership team activities, contributing to functional goals, priorities, and budgets
  • Leads and develops QC personnel, including oversight of training, performance, and team development
External Laboratory Oversight & Analytical Operations
  • Oversees external QC laboratories, including testing execution, data analysis, and issuance of Certificates of Analysis
  • Defines, tracks, and trends laboratory performance metrics (e.g., quality, capacity, turnaround time, non-conformances) to drive partner accountability and continuous improvement
  • Leads analytical troubleshooting efforts in collaboration with contract laboratories
  • Ensures alignment of external partners with program timelines to enable product disposition
Quality Systems, Compliance & Technical Execution
  • Reviews and approves analytical method qualification and validation protocols and reports
  • Authors, reviews, and approves stability protocols and reports and supports assignment of product expiry
  • Supports establishment of critical quality attributes (CQAs) and product specifications for Drug Substance (DS) and Drug Product (DP)
  • Partners with QA to ensure effective oversight of cGMP QC activities, including change control, deviations, investigations, CAPAs, and batch disposition support
  • Leads Out of Specification (OOS) and Out of Trend (OOT) investigations
  • Authors, reviews, and approves QC standard operating procedures
Regulatory, Inspection Readiness & Cross-Functional Collaboration
  • Prepares and reviews analytical CMC content for regulatory submissions (INDs, BLAs) and supports interactions with global health authorities
  • Participates in regulatory inspections and ensures inspection readiness across QC activities
  • Collaborates closely with Quality Assurance, Manufacturing, CMC, Supply Chain, Regulatory Affairs, and Project Management to align quality and program objectives
  • Oversees stability and reference standard programs to ensure compliance with regulatory expectations

Education and Skills Requirements: 

  • Bachelor's degree in Biology, Biochemistry, Chemistry, or related discipline; advanced degree (PhD) in Chemistry or Analytical Chemistry strongly preferred
  • 12+ years of experience in Analytical Development and/or Quality Control within a GMP-regulated environment
  • Strong expertise in analytical techniques (e.g., SEC, AEX, RP-HPLC, CE-SDS, icIEF, ELISA)
  • Deep knowledge of cGMP regulations and global guidance (FDA, ICH, EU)
  • Experience with compendial and product-specific analytical methods for biologics and/or small molecules
  • Demonstrated experience managing external QC laboratories and vendor performance
  • Experience supporting CMC regulatory submissions from IND through BLA and commercialization
  • Experience with oligonucleotide therapeutics, mass spectrometry, or bioanalytical assays is a plus
  • Proven leadership experience, including building and developing teams and driving organizational effectiveness
  • Strong strategic thinking and problem-solving capabilities with the ability to translate strategy into execution
  • Excellent interpersonal, communication, and negotiation skills with the ability to influence internal and external stakeholders
  • Highly collaborative leader who fosters cross-functional alignment and drives results in a fast-paced environment

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