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Senior Director Quality Systems Jobs (NOW HIRING)

Endo International

Sr. Director, Quality

Hobart, NY

Establish and ensure appropriate Quality Systems are implemented and maintained, including ongoing data analysis of product and process outputs to ensure early detection and response to quality ...

Cerapedics Inc

Senior Director, Quality

Westminster, CO · On-site

$197K - $285K/yr

As a Senior Director, Quality working on the Quality team, you will be empowered through meaningful ... Develops, implements, and oversees a Quality Management System that complies with domestic and ...

Align Technology

Director, Quality Systems

San Jose, CA · On-site

$196K - $269K/yr

Director, Quality Systems Department: Quality Employment Type: Full Time Location: US-California-San Jose Compensation: $196,000 - $269,500 / year Description We are seeking a dynamic and experienced ...

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Senior Director Quality Systems information

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$56.5K

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$227.5K

How much do senior director quality systems jobs pay per year?

As of Jun 15, 2026, the average yearly pay for senior director quality systems in the United States is $140,083.00, according to ZipRecruiter salary data. Most workers in this role earn between $103,000.00 and $169,000.00 per year, depending on experience, location, and employer.

What is the difference between Senior Director Quality Systems vs Quality Assurance Director?

AspectSenior Director Quality SystemsQuality Assurance Director
ResponsibilitiesOversees quality systems, compliance, and strategic quality initiatives across the organizationManages quality assurance activities, product testing, and compliance at the operational level
CredentialsTypically requires advanced degrees and extensive experience in quality systems and regulationsRequires relevant QA certifications and experience in quality control processes
Work EnvironmentStrategic, cross-departmental, executive-levelOperational, team-focused, often within manufacturing or R&D

The Senior Director Quality Systems focuses on strategic oversight and compliance of quality systems organization-wide, while the Quality Assurance Director concentrates on day-to-day QA activities and product quality assurance. Both roles require strong regulatory knowledge, but the Senior Director has a broader, more strategic scope.

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What cities are hiring for Senior Director Quality Systems jobs? Cities with the most Senior Director Quality Systems job openings:
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Senior Director Quality Systems jobs near you
Infographic showing various Senior Director Quality Systems job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 77% Full Time, and 22% Part Time. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $140,083 per year, or $67.3 per hour.

Senior Director, Quality Systems

Kailera Therapeutics, Inc.

Waltham, MA

Other

Posted 20 days ago

Job description

What You'll Do:

The Senior Director, Quality Systems is a high-impact leadership role responsible for the architecture, implementation, and continuous improvement of our Enterprise Quality Management System (eQMS). You will report to the Vice President, Quality and will serve as the primary architect of our quality framework, ensuring our global operations remain compliant with GxP standards while maintaining the agility required of a growing biotech.

Required location: Waltham, MA (hub-based, onsite 3-4 days per week)

Responsibilities:

  • Define and execute the long-term vision for the Quality Management System (QMS) to support global clinical development and future commercialization
  • Provide Quality oversight for GxP systems change controls. Support validation planning, execution, approvals
  • Act as the Business Owner for Veeva QualityVault. Lead the optimization of modules including Document Control, Training, Deviations, CAPA, and Change Control
  • Establish and lead Quality Management Reviews (QMR). Develop and report on Key Quality Indicators (KQIs) and metrics to senior leadership to drive proactive risk management
  • Ensure the QMS meets global regulatory requirements (FDA 21 CFR Parts 11, 210, 211, and 820; ICH E6; EudraLex Volume 4)
  • Lead the QMS strategy for inspection readiness. Serve as a key interface during regulatory inspections (FDA, EMA, etc.) and oversee the internal and vendor audit programs
  • Champion a culture of Quality. Streamline complex workflows to reduce cycle times for document approvals and deviation closures without compromising compliance
  • Build and mentor a high-performing team of Quality professionals, fostering a collaborative environment that balances technical rigor with pragmatic problem-solving

 

Required Qualifications:

  • 12+ years of experience in Quality Assurance within the Biotech/Pharmaceutical industry, with at least 5 years in a senior leadership capacity
  • Direct experience implementing or managing Veeva QualityVault is mandatory. You should be proficient in configuring workflows and leveraging the platform for data-driven decision-making
  • Proven track record in mid-sized companies navigating the transition from early-phase clinical trials to late-stage pivotal studies
  • Deep knowledge of global GxP regulations and experience participating in (or leading) successful regulatory inspections
  • Exceptional ability to translate complex quality requirements into actionable business strategies for non-quality stakeholders

 

Education:

  • Bachelor's degree required, scientific or engineering discipline preferred
  • Advanced degree preferred

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