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Qc Director Jobs (NOW HIRING)

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 ...

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 ...

Crusoe

Director, Quality Control

Dallas, TX · On-site

As Director of Quality Control , you will own the quality function across Crusoe's data center construction portfolio. You will set the standard - building the systems, frameworks, and team that ...

Crusoe

Director, Quality Control

Dallas, TX · On-site

As Director of Quality Control , you will own the quality function across Crusoe's data center construction portfolio. You will set the standard -- building the systems, frameworks, and team that ...

TScan Therapeutics

Director, Quality Control

Waltham, MA · On-site

$210K - $220K/yr

We are looking for an experienced professional to join our team as Director of QC, supporting release, characterization, and environmental monitoring (EM) testing for cellular drug products ...

Epoch Biodesign

Director, Quality Control

Dallas, TX · On-site

$188 - $235/hr

As Director of Quality Control , you will own the quality function across Crusoe's data center construction portfolio. You will set the standard -- building the systems, frameworks, and team that ...

TScan Therapeutics

Director, Quality Control

Waltham, MA · On-site

$210K - $220K/yr

We are looking for an experienced professional to join our team as Director of QC, supporting release, characterization, and environmental monitoring (EM) testing for cellular drug products ...

TScan Therapeutics

Director, Quality Control

Waltham, MA · On-site

$210K - $220K/yr

We are looking for an experienced professional to join our team as Director of QC, supporting release, characterization, and environmental monitoring (EM) testing for cellular drug products ...

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Qc Director information

See salary details

$31K

$125.6K

$213.5K

How much do qc director jobs pay per year?

As of Aug 18, 2026, the average yearly pay for qc director in the United States is $125,600.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,000.00 and $151,000.00 per year, depending on experience, location, and employer.

What is a QC director?

QC Directors, or Quality Control Directors, are senior professionals responsible for overseeing and managing the quality control processes within an organization. They develop quality standards, implement procedures, and ensure that products or services meet regulatory and company requirements. QC Directors lead quality teams, coordinate audits, and work to continuously improve quality systems. Their role is crucial for maintaining product reliability, customer satisfaction, and compliance with industry regulations.

What are the key skills and qualifications needed to thrive as a QC director?

To thrive as a QC Director, you need in-depth knowledge of quality control principles, regulatory standards (such as GMP or ISO), and significant experience in quality management, often supported by a science degree. Familiarity with laboratory information management systems (LIMS), statistical analysis software, and relevant quality certifications like Six Sigma or ASQ CQE is typically expected. Strong leadership, problem-solving, and communication skills are crucial for managing teams and collaborating across departments. These competencies ensure product quality, regulatory compliance, and continuous improvement within the organization.

What are some common challenges faced by a QC director in maintaining quality standards across multiple departments?

As a QC Director, one of the main challenges is ensuring consistent quality standards are upheld across various departments and production lines, especially in larger organizations. This often involves coordinating with cross-functional teams, managing compliance with regulatory requirements, and addressing discrepancies in processes or results. Effective communication, robust training programs, and regular audits are essential strategies used to overcome these challenges and foster a culture of continuous improvement.

What is the difference between Qc Director vs Quality Assurance Manager?

AspectQc DirectorQuality Assurance Manager
CredentialsOften requires a bachelor's degree in a related field, with many holding certifications like CQE or Six SigmaTypically requires a bachelor's degree, with certifications like CQE or Six Sigma common
Work EnvironmentOversees multiple departments or facilities, strategic planning, and high-level quality policiesFocuses on daily quality processes, team management, and implementing quality systems
Industry UsageUsed across manufacturing, pharmaceuticals, and engineering sectors for leadership rolesCommon in manufacturing, automotive, and consumer goods industries for operational quality roles

The Qc Director and Quality Assurance Manager roles share similar credentials and industry usage, but the director focuses on strategic oversight and leadership, while the manager handles daily quality operations. Both positions are vital for maintaining product quality and compliance.

What cities are hiring for Qc Director jobs?

Cities with the most Qc Director job openings:

What are the most commonly searched types of Qc jobs?

The most popular types of Qc jobs are:

What states have the most Qc Director jobs?

States with the most job openings for Qc Director jobs include:

Qc Director jobs near you
Infographic showing various Qc Director job openings in the United States as of August 2026, with employment types broken down into 2% As Needed, 83% Full Time, 12% Part Time, 1% Temporary, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $125,600 per year, or $60.4 per hour.

Director, Quality Control

Dyne Therapeutics

Waltham, MA

Full-time

Re-posted 12 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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