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Manager Of Quality Control Jobs (NOW HIRING)

V2X invites applications for the position of Director of Quality Control for the U.S. Department of ... Partner with the Capture Manager to shape the overall Program Management, Execution Approach, and ...

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The Manager of Quality Control is responsible for developing, implementing, and overseeing the Quality Management System (QMS) for heavy civil transportation projects delivered for state and federal ...

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The Manager of Quality Control is responsible for developing, implementing, and overseeing the Quality Management System (QMS) for heavy civil transportation projects delivered for state and federal ...

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The Manager of Quality Control is responsible for developing, implementing, and overseeing the Quality Management System (QMS) for heavy civil transportation projects delivered for state and federal ...

New

The Manager of Quality Control is responsible for developing, implementing, and overseeing the Quality Management System (QMS) for heavy civil transportation projects delivered for state and federal ...

New

The Manager of Quality Control is responsible for developing, implementing, and overseeing the Quality Management System (QMS) for heavy civil transportation projects delivered for state and federal ...

New

The Manager of Quality Control is responsible for developing, implementing, and overseeing the Quality Management System (QMS) for heavy civil transportation projects delivered for state and federal ...

New

The Manager of Quality Control is responsible for developing, implementing, and overseeing the Quality Management System (QMS) for heavy civil transportation projects delivered for state and federal ...

New

The Manager of Quality Control is responsible for developing, implementing, and overseeing the Quality Management System (QMS) for heavy civil transportation projects delivered for state and federal ...

The Manager of Quality Control is responsible for developing, implementing, and overseeing the Quality Management System (QMS) for heavy civil transportation projects delivered for state and federal ...

New

The Manager of Quality Control is responsible for developing, implementing, and overseeing the Quality Management System (QMS) for heavy civil transportation projects delivered for state and federal ...

New

The Manager of Quality Control is responsible for developing, implementing, and overseeing the Quality Management System (QMS) for heavy civil transportation projects delivered for state and federal ...

The Manager of Quality Control is responsible for developing, implementing, and overseeing the Quality Management System (QMS) for heavy civil transportation projects delivered for state and federal ...

New

The Manager of Quality Control is responsible for developing, implementing, and overseeing the Quality Management System (QMS) for heavy civil transportation projects delivered for state and federal ...

New

The Manager of Quality Control is responsible for developing, implementing, and overseeing the Quality Management System (QMS) for heavy civil transportation projects delivered for state and federal ...

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Manager Of Quality Control information

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$30.5K

$81.3K

$129.5K

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

As of Jul 18, 2026, the average yearly pay for manager of quality control in the United States is $81,324.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $100,000.00 per year, depending on experience, location, and employer.

How much do QC managers make in the US?

Quality Control (QC) managers in the US typically earn an average salary between $70,000 and $110,000 annually, depending on experience, industry, and location. They often oversee quality assurance processes, implement standards, and may hold certifications such as Six Sigma or ISO auditor credentials.

What are some common challenges faced by a Manager of Quality Control, and how can they be addressed?

A Manager of Quality Control often encounters challenges such as maintaining consistent quality standards across multiple shifts or teams, managing tight production deadlines while upholding compliance, and implementing new quality protocols. Addressing these challenges requires strong communication skills, effective training programs, and a proactive approach to problem-solving. Collaborating closely with production, engineering, and regulatory teams helps ensure that quality objectives are aligned with business goals, and regular audits or process reviews can help identify and resolve issues early.

What is the difference between Manager Of Quality Control vs Quality Control Supervisor?

AspectManager Of Quality ControlQuality Control Supervisor
CertificationsISO 9001, Six Sigma, Quality Management certificationsISO 9001, Six Sigma (preferred but not always required)
Work EnvironmentOversees multiple teams, strategic planning, higher-level managementSupervises daily quality control activities, team management
Industry UsageUsed across manufacturing, pharmaceuticals, food productionCommon in manufacturing, production facilities

The Manager Of Quality Control typically holds a higher strategic role, overseeing quality assurance processes and managing teams, while the Quality Control Supervisor focuses on daily operations and team supervision. Both roles require similar certifications and are integral in maintaining product standards within the same industries.

What is the salary of a QA manager?

The salary of a Quality Assurance (QA) Manager typically ranges from $70,000 to $120,000 annually, depending on experience, industry, and location. QA managers often oversee testing teams, implement quality standards, and may hold certifications like Six Sigma or ISTQB to enhance their earning potential.

Is QC a high paying job?

The salary for a Manager of Quality Control varies depending on industry, experience, and location, but it is generally considered a well-paying role with salaries often above the median for managerial positions. Professionals in QC management with certifications and technical skills can earn higher wages, especially in manufacturing, pharmaceuticals, or technology sectors.

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

To thrive as a Manager of Quality Control, you need expertise in quality assurance processes, statistical analysis, and regulatory compliance, typically supported by a relevant degree and experience in quality management. Familiarity with quality management systems (such as ISO 9001), Six Sigma or Lean certifications, and proficiency with data analysis tools are commonly required. Strong leadership, problem-solving abilities, and effective communication are vital soft skills in this role. These skills ensure consistent product quality, regulatory adherence, and efficient team performance, which are critical for organizational success.

What does a Manager of Quality Control do?

A Manager of Quality Control oversees the quality assurance processes within an organization to ensure that products or services meet established standards. They develop and implement quality control procedures, lead a team of quality inspectors, and work closely with production and engineering teams to resolve quality issues. Additionally, they analyze data, conduct audits, and recommend improvements to enhance product reliability and customer satisfaction.

What does a quality control manager do?

A quality control manager oversees the inspection and testing of products or services to ensure they meet quality standards and regulatory requirements. They develop quality procedures, analyze data, and coordinate with production teams to address issues and improve processes. Strong attention to detail, leadership skills, and knowledge of quality management tools like ISO standards are essential for this role.
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What are the most commonly searched types of Of Quality Control jobs? The most popular types of Of Quality Control jobs are:
What states have the most Manager Of Quality Control jobs? States with the most job openings for Manager Of Quality Control jobs include:
Director of Quality Control

Director of Quality Control

Nivagen Pharmaceuticals

Sacramento, CA โ€ข On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 5 days ago


Job description

About the Company:
Nivagen is a global company devoted to improving lives by developing high-quality, affordable generic prescription drugs and over-the-counter products for the North American market. For over a decade, we have remained committed to our core values of excellence, integrity, and respect for people. Our dedicated team works collaboratively to advance manufacturing, distribution, and quality control, taking a comprehensive approach to healthcare. Through vertical integration of the pharmaceutical supply chain, state-of-the-art technology, and an unwavering focus on excellence, we continually strive to enhance medication accessibility and affordability.
We prioritize our employees' well-being by offering competitive pay, comprehensive benefits, and strong training and development programs. By investing in our workforce and nurturing a culture of growth and support, we empower our team to drive innovation and make a positive impact in healthcare. Our mission at Nivagen is clear: to improve lives by providing high-quality, affordable medications while upholding the highest standards of integrity and excellence.
As a leader in pharmaceutical manufacturing, Nivagen is committed to producing sterile products that meet the healthcare industry's rigorous demands. Specializing in the production of vials, pre-filled syringes (PFS), and IV bags, we aim to make a meaningful impact on patient care. Join our team to help push the boundaries of sterile manufacturing, achieving the highest standards in safety, quality, and operational efficiency.
Job Location:
Nivagen Pharmaceuticals, Sacramento, CA
3900 Duckhorn Dr, Sacramento, CA 95834
About the Job:
Title of the Position: Director of Quality Control
Department: Quality Control
Reports to: Head of Quality
The Director of Quality Control leads all QC operations within a pharmaceutical manufacturing facility, ensuring reliable, compliant testing that meets regulatory expectations and supports timely product release. This role oversees QC laboratories (chemistry, microbiology, analytical development support, raw materials, stability, and in-process testing), manages scientific and operational strategy, drives continuous improvement, and ensures data integrity and regulatory compliance across all laboratory activities.
Responsibilities:
  • Leadership & Management
    • Provide strategic leadership for QC teams, including chemistry, microbiology, stability, and raw materials testing.
    • Develop and mentor QC managers, supervisors, and analysts to ensure strong technical capability and compliance culture.
    • Establish resource plans, staffing, skills development, and succession planning.
    • Set performance expectations, conduct performance reviews, and manage career development.

    Laboratory Operations & Oversight
    • Direct day-to-day QC operations to support manufacturing schedules, ensuring on-time testing and release.
    • Oversee testing for raw materials, in-process samples, finished products, environmental monitoring, and stability programs.
    • Ensure proper functioning, maintenance, and qualification/calibration of all lab equipment.
    • Oversee sample management, laboratory workflows, and prioritization.
    • Implement robust OOS/OOT/OOE processes and drive investigations to scientifically sound conclusions.

    Regulatory Compliance & Quality Systems
    • Ensure all QC activities comply with cGMP, FDA/EMA/ICH guidelines, USP/EP/JV standards, and company SOPs.
    • Own and maintain quality systems related to laboratory operations, including:
      • Change control
      • Deviations and investigations
      • CAPA management
      • Document control
      • Data integrity program
    • Prepare for and lead QC aspects of regulatory inspections and internal/external audits.
    • Ensure laboratory data integrity practices meet ALCOA+ principles.

    Analytical Strategy & Method Management
    • Oversee method validation, verification, transfer, and lifecycle management activities.
    • Evaluate and implement new analytical technologies to improve QC reliability, efficiency, and scientific rigor.
    • Collaborate with R&D/Analytical Development to ensure smooth tech transfer of analytical methods and specifications.
    • Ensure the QC team supports process changes, comparability studies, and product lifecycle management.

    Stability Program Management
    • Oversee design, execution, and monitoring of stability studies in compliance with ICH guidelines.
    • Ensure timely stability testing and trend analysis to support expiry dating, regulatory filings, and ongoing product quality review.

    Quality Metrics & Continuous Improvement
    • Develop, track, and report quality metrics (e.g., OOS rate, lab investigation cycle time, test turnaround time, EM trends).
    • Drive continuous improvement initiatives such as Lean lab practices, automation, and digitalization.
    • Optimize laboratory workflows for efficiency while maintaining compliance and data integrity.

    Cross-Functional Collaboration
    • Act as a QC subject matter expert in cross-functional teams, including QA, Manufacturing, Regulatory Affairs, Supply Chain, and R&D.
    • Participate in material/vendor qualification, change control reviews, and deviation boards.
    • Support regulatory submissions by providing QC data, summary reports, and responses to agency questions.

Qualifications:
Education/Experience:
  • Master's or PhD in Chemistry, Biochemistry, Microbiology, Pharmaceutical Sciences, or related discipline preferred.
  • A bachelor's degree with extensive experience may be considered.
  • 10+ years of experience in QC within pharmaceutical or biopharmaceutical manufacturing.
  • 5+ years of leadership/management experience in a GMP laboratory setting.
  • Experience preparing for and hosting inspections by FDA, EMA, or other health authorities.
  • Strong background in analytical chemistry and/or microbiology.
  • Experience with method validation, QC automation, LIMS/ELN, and electronic data management systems.

Knowledge, Skills, and Abilities:
  • Deep knowledge of cGMP, ICH guidelines, USP/EP, and regulatory expectations.
  • Strong scientific judgment and technical problem-solving skills.
  • Excellent leadership, communication, and interpersonal skills.
  • Ability to manage multiple priorities and drive timely execution.
  • Demonstrated ability to develop high-performing teams and a culture of quality and compliance.

Requirements:
  • Must live or be willing to move to the Sacramento Metropolitan Region (Approx 40 miles' radius)

Benefits:
  • Pay range: Competitive Salary Range $120k - $150k Annually
  • Yearly bonus eligibility
  • Benefits: Nivagen offers a wide variety of benefits and programs to support health and well-being (Medical, dental, and vision coverage)
  • Paid time off plan
  • 401 (k) savings plan

Additional Information:
Nivagen to afford equal opportunity for employment to all individuals regardless of race, color, age, national origin, physical or mental disability, history of disability, ancestry, citizenship status, political affiliation, religion, gender, transgender, gender identity, marital status, status as a parent, sexual orientation, veteran status, genetic information or other factors prohibited by law, and to prohibit harassment or retaliation based on any of these factors.