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Vice President Quality Control Jobs (NOW HIRING)

Vice President, Quality Full Time Sr.Mgmt: Dir&Up Miami, FL, US Position Summary The Vice President ... Responsible for the Quality Control function as it pertains to Environmental Monitoring and Quality ...

Vice President, Quality The Vice President of Quality will lead the development, execution, and ... control, and rapid escalation of out‑of‑control conditions. Essential Duties and ...

Vice President Quality****Job Category:**Quality**Job Level:**Level B**Job Location:** Aiken, SC**Why Join Rolls-Royce?**At Rolls-Royce, we take pride in being a business that has played a pivotal ...

Vice President, Quality Full Time Sr.Mgmt: Dir&Up Miami, FL, US 30+ days ago Requisition ID: 1674 ... Responsible for the Quality Control function as it pertains to Environmental Monitoring and Quality ...

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Vice President Quality Job Category: Quality Job Level: Level B Job Location: Aiken, SC Role Overview The Vice President, Quality leads the North America Quality organization, including Production ...

The VP, Quality serves as the chief steward of the company's quality vision, culture, and systems ... QP release, and document control. * Develop and implement quality processes, systems, and ...

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Position The Vice President, Quality for Space, Defense, & National Security is responsible for ... Lead enterprise-wide quality, compliance, and control efforts across aerospace and other highly ...

The Vice President, Quality for Space, Defense, & National Security is responsible for leading ... Lead enterprise-wide quality, compliance, and control efforts across aerospace and other highly ...

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Vice President Quality Control information

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$31K

$125.6K

$213.5K

How much do vice president quality control jobs pay per year?

As of Jul 10, 2026, the average yearly pay for vice president quality control 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 are the main challenges faced by a Vice President of Quality Control, and how can they be addressed?

A Vice President of Quality Control often faces challenges such as ensuring compliance with evolving regulatory standards, managing cross-functional teams, and maintaining high-quality output across diverse product lines. Addressing these challenges requires strong leadership, effective communication, and a continuous improvement mindset. Building robust quality management systems, fostering a culture of accountability, and staying updated with industry regulations are essential strategies to overcome these hurdles and drive organizational success.

What are the key skills and qualifications needed to thrive as a Vice President Quality Control, and why are they important?

To thrive as a Vice President Quality Control, you need deep expertise in quality management systems, regulatory compliance, and process improvement, often supported by an advanced degree in science or engineering and significant industry experience. Familiarity with quality management software, Six Sigma or Lean certifications, and regulatory standards such as ISO 9001 is typically required. Exceptional leadership, strategic thinking, and communication skills are crucial for driving quality initiatives and fostering a culture of excellence. These skills ensure that products and processes consistently meet high standards, minimize risk, and support the organization's reputation and regulatory compliance.

What does a Vice President of Quality Control do?

A Vice President of Quality Control is responsible for overseeing and directing all quality assurance and quality control activities within an organization. They develop strategies, set quality standards, and ensure that products or services meet regulatory and company requirements. The VP of Quality Control leads teams, implements process improvements, and coordinates with other departments to resolve quality-related issues. Their role is critical in maintaining customer satisfaction, minimizing defects, and ensuring compliance with industry standards.
What cities are hiring for Vice President Quality Control jobs? Cities with the most Vice President Quality Control job openings:
What are the most commonly searched types of Quality Control jobs? The most popular types of Quality Control jobs are:
What states have the most Vice President Quality Control jobs? States with the most job openings for Vice President Quality Control jobs include:
Infographic showing various Vice President Quality Control job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 76% Full Time, 19% Part Time, 1% Temporary, and 3% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $125,600 per year, or $60.4 per hour.

Executive Director/VP Quality and Regulatory

GTS Scientific

Princeton, NJ

Full-time

Posted 23 days ago


Job description

Executive Director/VP Quality and RegulatoryExecutive Director/VP Quality and Regulatory

Direct message the job poster from GTS Scientific

Executive Director/VP Quality and Regulatory

Location: On-site (with flexibility for hybrid work)

Travel: ~15–20% domestic/international

Position Summary

A growing, global contract services provider in the pharmaceutical industry is seeking an accomplished Executive Director/VP Quality and Regulatory. This executive leader will oversee the Quality Assurance, Quality Control, and Regulatory Affairs functions for a dynamic organization focused on commercial drug manufacturing and clinical trial supply chain services.

The role requires deep expertise in global regulatory compliance (FDA, EMA, etc.), strong leadership in quality systems, and experience navigating both commercial and clinical operations within a regulated GxP environment.

Strategic Leadership

  • Define and execute the Quality and Regulatory strategy in alignment with enterprise growth goals.
  • Participate in senior leadership forums to guide overall business direction and risk management.
  • Serve as the primary Quality and Regulatory representative in client, regulatory, and external stakeholder engagements.

Quality Assurance & Systems

  • Lead quality oversight across manufacturing, packaging, labeling, and distribution.
  • Ensure compliance with cGMP (21 CFR Parts 210/211), EU GMPs, and ICH standards.
  • Maintain audit readiness and drive continuous improvement across all quality operations.
  • Track and enhance quality performance metrics (e.g., deviations, CAPAs, complaint trends).

Regulatory Affairs

  • Develop and manage regulatory compliance strategies across all product lifecycle stages.
  • Interpret and implement evolving global regulatory requirements.
  • Direct preparation of regulatory filings including site registrations and amendments.
  • Act as a liaison with regulatory agencies and client representatives.

Clinical Supply Chain Compliance

  • Ensure compliance with GCP, GMP, and GDP in clinical packaging, labeling, and distribution.
  • Oversee qualification of depots, shipping lanes, and cold chain systems.
  • Maintain controls over investigational product handling, reconciliation, and destruction.

Leadership & Talent Development

  • Lead and develop a high-performing, technically strong Quality & Regulatory team.
  • Ensure team resourcing, capability building, and training keep pace with company growth.
  • Promote cross-functional collaboration with operations, supply chain, and commercial teams.

Qualifications

Education

  • Bachelor’s degree in a scientific or technical field required (Pharmacy, Chemistry, Biology, Engineering, etc.)
  • Advanced degree (MS, PharmD, PhD, MBA) preferred.

Experience

  • 15+ years of progressive leadership in pharmaceutical quality and regulatory functions.
  • Minimum 5 years in an executive/senior leadership role.
  • Experience in a contract development and manufacturing or clinical supply environment is strongly preferred.
  • Demonstrated success managing global regulatory inspections and audits.
  • Familiarity with sterile, oral solid dose, or biologic drug manufacturing is a plus.

Core Competencies

  • Expert knowledge of cGMP, GDP, GCP, ICH, and global regulatory expectations.
  • Strategic and operational leadership with executive presence.
  • Strong decision-making, analytical thinking, and communication skills.
  • Proven ability to thrive in a fast-paced, client-driven organization.
Seniority level
  • Seniority levelExecutive
Employment type
  • Employment typeFull-time
Job function
  • Job functionQuality Assurance
  • IndustriesPharmaceutical Manufacturing

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