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Head Of Quality Control Jobs (NOW HIRING)

The ICE Group

Head of Quality Engineering

Newark, CA · Remote

The Leader of Quality Engineering is responsible for creating a test-driven culture resulting in high quality products delivered to market on time that drive the highest levels of customer ...

Evotec

EVP, Global Head of Quality

Princeton, NJ · On-site

As Global Head of Quality, you will: * Define and drive Evotec's global Quality strategy across Drug Discovery and Drug Development * Lead large-scale transformation initiatives across systems ...

MayTec Inc.

Head of Quality Assurance, Global

Gilbert, AZ · On-site

$70K - $100K/yr

Leads the development and implementation of policies, procedures, and process improvements that strengthen quality assurance and control while supporting efficient material flow through MayTec ...

BMSC

Director of Quality

Fort Worth, TX · On-site

As head of the Quality department, the position sets the standard for quality throughout the ... Design and develop new quality control processes to improve efficiency and consistency including ...

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Head Of Quality Control information

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$31K

$125.6K

$213.5K

How much do head of quality control jobs pay per year?

As of Jul 13, 2026, the average yearly pay for head of 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 is the difference between Head Of Quality Control vs Quality Assurance Manager?

AspectHead Of Quality ControlQuality Assurance Manager
ResponsibilitiesOversees quality control processes, inspects products, ensures compliance with standardsDevelops quality assurance policies, manages audits, improves quality systems
CertificationsISO 9001, Six Sigma, Quality Control certificationsISO 9001, Six Sigma, Quality Management certifications
Work EnvironmentManufacturing, production lines, labsOffice settings, quality departments, cross-functional teams
FocusProduct inspection and defect detectionProcess improvement and system compliance

The Head Of Quality Control primarily focuses on inspecting products and ensuring quality standards are met during manufacturing. In contrast, the Quality Assurance Manager develops and manages quality systems to prevent defects and improve processes. Both roles require similar certifications and work in related environments, but their core responsibilities differ in scope and focus.

What does a Head of Quality Control do?

A Head of Quality Control is responsible for overseeing and managing the quality assurance processes within an organization. They develop, implement, and maintain systems to ensure products or services meet established standards and comply with relevant regulations. This role involves leading quality control teams, analyzing data to identify areas for improvement, and collaborating with other departments to resolve quality issues. Ultimately, the Head of Quality Control ensures that the organization's output consistently meets customer and regulatory expectations.

What does the head of quality control do?

The head of quality control oversees the quality assurance processes within an organization, ensuring products or services meet specified standards. They develop testing procedures, analyze quality data, and coordinate with production teams to implement improvements, often requiring knowledge of industry regulations and quality management tools. This role typically involves leadership, problem-solving, and certification in quality standards such as ISO.

What are the main challenges a Head of Quality Control faces when implementing new quality standards across multiple departments?

One of the main challenges for a Head of Quality Control is ensuring consistent adoption of new quality standards across various departments, each with their own processes and priorities. This often involves extensive cross-functional collaboration, clear communication, and ongoing training to align teams and address resistance to change. Additionally, monitoring compliance and measuring the effectiveness of these standards require robust data collection and analysis systems. Successfully navigating these challenges not only improves product quality but also strengthens the organization's overall quality culture.

How much do QC managers make in the US?

Quality Control (QC) managers in the US typically earn between $70,000 and $120,000 annually, depending on experience, industry, and location. Salaries can be higher with certifications such as Six Sigma or ISO auditor credentials, and roles often require strong leadership and knowledge of quality management systems.

Which pays more, QA or QC?

In the quality assurance (QA) and quality control (QC) fields, QA roles typically offer higher salaries due to their focus on process improvement and prevention, often requiring skills in auditing and management. QC roles, which focus on product inspection and testing, tend to have slightly lower pay but may require technical testing skills and certifications. Salary differences can vary based on industry, experience, and location.

What jobs pay $500,000 a year in the US?

High-level executive roles such as CEOs, CFOs, and other C-suite positions often reach or exceed $500,000 annually, especially in large corporations. Certain specialized roles like investment bankers, senior surgeons, and successful entrepreneurs can also earn this level of income, often supplemented by bonuses, stock options, or profit sharing. These positions typically require extensive experience, advanced skills, and significant responsibility.

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

To thrive as a Head Of Quality Control, you need deep expertise in quality assurance methodologies, regulatory compliance, and process improvement, usually supported by a degree in a relevant field and significant industry experience. Familiarity with quality management systems (QMS), ISO standards, and statistical analysis tools is typically required, along with certifications like Six Sigma or ASQ. Strong leadership, problem-solving abilities, and excellent communication skills help drive team performance and foster a culture of continuous improvement. These skills ensure product consistency, regulatory compliance, and operational efficiency, all of which are crucial for organizational reputation and success.
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Head Of Quality Control jobs near you
Infographic showing various Head Of 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.
Senior Director of Quality Control

Senior Director of Quality Control

Ratio Therapeutics, Inc.

West Valley City, UT • On-site

Full-time

Posted yesterday

Job description

About Ratio Therapeutics
Ratio Therapeutics is committed to improving and extending the lives of cancer patients without sacrificing their quality of life. We are a team of passionate scientists, engineers, and business professionals dedicated to advancing the field of targeted radioligand therapy. To accomplish this, we utilize our proprietary TRILLIUM™ and MACROPA™ platforms: TRILLIUM™ allows fine-tuning of radioligand pharmacokinetics thereby enhancing the therapeutic index, while MACROPA™ simplifies the manufacturing process for the alpha-emitting isotope, actinium-225. These enabling platform technologies to have resulted in an emergent pipeline of novel therapeutic candidates. We are looking for talented, dedicated, and creative individuals eager to help us advance these technologies from discovery research through clinical development. Join us in our quest to become the leading innovator in radioligand therapy and improve the lives of cancer patients and their families.
About the Position
Ratio is seeking an on-site Senior Director of Quality Control (QC) for our Salt Lake City, Utah radiopharmaceutical manufacturing facility. As the Senior Director, QC, you will be the primary architect and hands-on implementer of the analytical and microbiological testing infrastructure for our new state-of-the-art radiopharmaceutical manufacturing facility. During the initial build-out, you will design the systems, workflows, and procedures that will scale with the team. You will be supported by initial analytical and microbiology staff and cross-functional partners, with clear plans to recruit and onboard additional QC personnel as volume increases and day-to-day QC testing demand grows.
Key Responsibilities:
Analytical Method Development, Optimization, and Validation
• Method Lifecycle Management: Lead the end-to-end lifecycle of analytical methods, from initial development through phase-appropriate validation (ICH Q2) and into routine commercial use.
• Equipment Qualification: Oversee the IQ/OQ/PQ of specialized QC instrumentation, including HPLC with radioactivity detectors, Gamma Spectrometers, instant thin layer chromatography, and Gas Chromatographs.
• Stability Programs: Design and manage stability studies to support shelf-life claims for both drug substances and finished drug products, accounting for radiolytic degradation.
Quality Systems & Regulatory Compliance
• Document & Systems Development: Design, author, and implement critical QC Laboratory documentation, such as SOPs, Work Instructions, Testing Specifications, etc. to support sample workflow management and data integrity principles.
• Data Integrity & 21 CFR §11: Implement and maintain "Data Integrity by Design" for all lab informatics (LMS, CDS), ensuring all electronic records are contemporaneous, attributable, and secure.
• Investigations & Troubleshooting: Lead the technical investigation of Out-of-Specification (OOS) results, Out-of-Trend (OOT) data, and lab deviations, utilizing root-cause analysis (RCA) to drive effective CAPAs.
• Audit Readiness: Act as the primary subject matter expert during FDA, state, and NRC inspections, defending analytical methodologies and microbiological control strategies.
• CMC Support: Author and review relevant sections of IND/NDA/ANDA filings, ensuring technical data accurately reflects the validated state of the QC laboratory.
Operational Leadership & Team Development
• Hands-On Leadership: Work in close collaboration with QC analysts, microbiologists, and cross-site SMEs to ensure adequate bench support, redundancy, and coverage for release testing and troubleshooting while the QC Team is being built.
• SME Management: Mentor a diverse team of subject matter experts, fostering a culture of technical excellence and collaborative problem-solving between the analytical and micro sub-departments.
• Resource Planning: Develop and manage the QC department budget, including capital expenditure on lab buildouts and the procurement of reagents and reference standards.
• KPI Tracking: Establish and monitor departmental metrics (e.g., sample turnaround time, lab error rates) to ensure the QC lab meets the operational demands of the production schedule.
Laboratory Informatics (CDS/LIMS)
• Serve as business owner for Waters Empower chromatography data system (CDS), including user administration, system suitability configuration, and integration with QC workflows.
• Lead the configuration and implementation of Waters NuGenesis LMS for sample management, stability pulls, and data review/approval, ensuring alignment with data integrity requirements.
• Partner with IT and vendors to qualify, maintain, and continuously improve the CDS and LIMS environments.
Qualifications:
• PhD and 10+ years, MS and 15+ Years, or BS and 20+ years in Quality Control within Life Sciences, with a minimum of 5 years specifically in radiopharmaceutical manufacturing.
• Proven track record in analytical method development and validation through the commercial drug product lifecycle.
• Advanced degree in chemistry, or related scientific discipline.
• Thorough knowledge of ICH Q2, USP <1225>, 21 CFR Part §211 and 21 CFR §11.
• Preferred experience developing PET/therapeutic radiopharmaceutical analytical testing methodology
• Direct, hands-on experience using and administering Waters Empower 3 CDS in a GMP QC laboratory, including method set-up, integration parameters, and secure data review/approval workflows.
• Direct, hands-on experience implementing and/or administering Waters NuGenesis LMS (or similar LIMS), from user requirement definition through validation and routine use.
• Comfortable working as a hands-on laboratory leader while a broader QC team is being recruited, with the expectation of building, mentoring, and delegating to that team over time.
• Demonstrated experience managing professional-level SMEs and building lab cultures centered on integrity and continuous improvement.
The annual base salary for this role is expected to range between $205,000.00 and $240,000.00. This range is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. The actual base salary offered will depend on a variety of factors, including qualifications, work experience, skills, level of education attained, certifications or other professional licenses held, the location in which the applicant lives and/or from which they will be performing the job, and other job-related factors permitted by law.

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