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Vice President Qa Ra Jobs (NOW HIRING)

QT Imaging, Inc.

Senior QA/RA Specialist

Novato, CA · On-site

$96K - $133K/yr

Serve as the primary QA/RA representative on cross-functional project teams, ensuring quality and regulatory requirements are incorporated throughout the product lifecycle. * Lead document control ...

NC SECU

VP QA Engineering

Raleigh, NC · On-site

Quality Assurance leader in Information Technology responsible for leading teams of QA Engineers and Performance Engineers delivering testing services with a focus on automation and performance.

Daikin Applied

Vice President, Quality

Plymouth, MN · On-site

The Vice President Quality will provide strategic thought and execution leadership required to ... Provide governance for Quality Assurance and New Product Introduction (NPI) processes, while ...

Bosch-HomeComfort

VP - Quality, Americas

Dallas, TX · On-site

The VP - Quality will drive a culture of continuous improvement, operational excellence, and customer focus while leading quality initiatives across multiple manufacturing and distribution sites.

Bosch Group

VP - Quality, Americas

Dallas, TX · On-site

The VP - Quality will drive a culture of continuous improvement, operational excellence, and customer focus while leading quality initiatives across multiple manufacturing and distribution sites.

Bosch-HomeComfort

VP - Quality, Americas

Dallas, TX · On-site

The VP - Quality will drive a culture of continuous improvement, operational excellence, and customer focus while leading quality initiatives across multiple manufacturing and distribution sites.

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$43.5K

$157.5K

$277.5K

How much do vice president qa ra jobs pay per year?

As of Sep 12, 2026, the average yearly pay for vice president qa ra in the United States is $157,532.00, according to ZipRecruiter salary data. Most workers in this role earn between $115,000.00 and $190,000.00 per year, depending on experience, location, and employer.

What is a vice president QA RA?

A Vice President of QA RA (Quality Assurance and Regulatory Affairs) is a senior executive responsible for overseeing an organization's quality systems and ensuring compliance with regulatory requirements, particularly in highly regulated industries like pharmaceuticals, medical devices, or biotechnology. They lead teams that develop and implement quality standards, manage audits, and interact with regulatory agencies to ensure products meet safety and efficacy guidelines. This role requires both strategic leadership and deep knowledge of regulatory frameworks to minimize risk and support product approvals. The VP of QA RA also collaborates with other departments to integrate quality and compliance into business processes.

What are the key skills and qualifications needed to thrive as a vice president QA RA?

To excel as a Vice President of QA/RA (Quality Assurance/Regulatory Affairs), you need deep expertise in quality systems, regulatory compliance, and industry standards, usually supported by a relevant science or engineering degree and extensive experience in regulated environments. Familiarity with tools like electronic quality management systems (eQMS), regulatory submission platforms, and certifications such as RAC or Six Sigma are commonly expected. Strategic leadership, strong communication, and problem-solving skills help drive cross-functional initiatives and foster a culture of compliance. These capabilities are critical for ensuring product quality, maintaining regulatory approval, and mitigating business risk in highly regulated industries.

How does a vice president QA RA typically collaborate with cross-functional teams to ensure compliance and product quality?

A Vice President of QA/RA (Quality Assurance/Regulatory Affairs) regularly works with R&D, manufacturing, marketing, and legal teams to ensure products meet regulatory standards and maintain high quality. They lead cross-functional meetings to align on compliance requirements, oversee risk assessments, and guide teams in implementing quality systems. Effective collaboration is essential for timely product approvals and market launches, as QA/RA leaders often interpret regulations and translate them into actionable steps across departments. This role requires strong communication and leadership skills to drive a culture of compliance and continuous improvement.

What is the difference between Vice President Qa Ra vs Quality Assurance Manager?

AspectVice President Qa RaQuality Assurance Manager
ResponsibilitiesOversees quality and regulatory strategies at an organizational level, sets policies, and manages multiple teams.Manages daily quality assurance operations, implements testing procedures, and ensures product compliance.
CredentialsTypically requires advanced degrees (e.g., MBA, related certifications), extensive industry experience.Requires relevant certifications (e.g., CQE, Six Sigma), and experience in quality management.
Work EnvironmentExecutive-level, strategic planning, cross-departmental collaboration.Operational, team management, hands-on testing and process improvement.

The Vice President Qa Ra focuses on strategic leadership and regulatory compliance at an organizational level, while the Quality Assurance Manager handles daily QA operations and product testing. Both roles require quality-related credentials, but the VP role emphasizes broader strategic oversight.

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Vice President Qa Ra jobs near you
Infographic showing various Vice President Qa Ra job openings in the United States as of September 2026, with employment types broken down into 95% Full Time, and 5% Part Time. Highlights an 85% Physical, 6% Hybrid, and 9% Remote job distribution, with an average salary of $157,532 per year, or $75.7 per hour.

Vice President, Quality Control

Needham, MA • On-site

Candel Therapeutics
Biotechnology Research and Development • 51 - 200 employees
Learn more about Candel Therapeuticsexternal

$290K - $335K/yr

Full-time

Posted 26 days ago

Job description

Hybrid role: (2-3 days a week in Needham office)
Salary: $290K - $335K
Why Work With Us?
At Candel, our people drive our success. We value diversity, collaboration, and bold thinking in a supportive, mission-driven environment. Like a team, we show up for each other and stay focused on making a difference for patients and families. Our leadership is transparent and empowering, and our culture is built on trust, flexibility, and accountability, encouraging ownership and innovation every day.
Our Science: Advancing Cancer Immunotherapies
Candel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies that stimulate personalized, systemic anti-tumor responses. Our platforms use genetically modified adenovirus and HSV constructs. With positive Phase 3 results for our lead candidate, it's an exciting time to join us and help bring transformative cancer treatments to patients. Learn more:www.candeltx.com
Position Summary
The Vice President, Quality Control will provide strategic, technical, and operational leadership for all Quality Control functions supporting the development, manufacture, release, and lifecycle management of viral vector and advanced therapy products. This role serves as a key member of the CMC and Quality leadership team, ensuring that QC strategy, laboratory operations, and data integrity systems align with regulatory requirements, product quality objectives, and commercial readiness. The VP, Quality Control will oversee testing strategies, specification setting, method qualification/validation, transfer, and lifecycle management of QC systems supporting both clinical and commercial programs.Key Interfaces
This role will work closely with CMC leadership, Analytical Development, Process Development, Manufacturing, Quality Assurance, Regulatory Affairs, Clinical Development, Supply Chain, Program Management, external laboratories (CROs/CDMOs), and executive leadership.Key Responsibilities
  • Establish and lead the global Quality Control strategy, including laboratory infrastructure, testing frameworks, and lifecycle management across development and commercial programs.
  • Provide governance and oversight for QC systems including specifications, test methods, environmental monitoring, stability programs, reference standards, and batch release support.
  • Ensure QC activities are compliant with global regulatory requirements (FDA, EMA, ICH) including cGMP expectations and data integrity standards.
  • Lead method qualification, validation, transfer, and performance monitoring in partnership with Analytical Development.
  • Oversee internal and external laboratory operations, including CROs and CDMOs.
  • Drive QC support for manufacturing operations including in-process, release, and stability testing.
  • Provide leadership for OOS/OOT investigations, deviations, and CAPA implementation.
  • Support regulatory submissions and inspections in collaboration with QA and Regulatory Affairs.
  • Advance QC through digital transformation, automation, and laboratory systems (LIMS, ELN).
  • Build and lead a high-performing QC organization.
  • Manage budgets, capital planning, and resources aligned to program priorities.
Required Qualifications
  • Advanced degree in a scientific discipline preferred or equivalent experience.
  • 15+ years of experience in Quality Control in the biopharmaceutical industry.
  • Experience supporting biologics, viral vector, or advanced therapy products.
  • Strong knowledge of QC systems including validation, microbiology, stability, and data integrity.
  • Experience with global regulatory submissions and inspections.
  • Proven leadership and team management capabilities.
Preferred Qualifications
  • Experience building or transforming QC organizations.
  • Experience with advanced therapy modalities (gene therapy, viral vectors).
  • Experience implementing digital QC systems.
  • Experience managing external laboratory networks.
  • Industry leadership through publications or regulatory engagement.
Leadership Competencies
  • Strategic leadership with strong quality and regulatory expertise.
  • Ability to influence cross-functional teams.
  • Strong risk-based decision making.
  • Commitment to quality culture and inspection readiness.
  • Excellent communication skills.

Must be authorized to work in US. We cannot provide sponsorships.
We are not open to agency resume submissions at this time

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