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Director Of Quality Control Jobs (NOW HIRING)

Pine Pharmaceuticals

Director of Quality

Tonawanda, NY · On-site

This includes oversight of quality assurance, quality control, compliance programs, risk management ... The Director of Quality leads, mentors, and develops the quality organization by building high ...

Curia, Inc.

Director, Quality Control

Albuquerque, NM · On-site

The Director of Quality Control (QC) is responsible for leading the Quality Control Unit (Microbiology & Chemistry) at the site and for providing analytical technical guidance to the various site ...

LGM Pharma, LLC

DIRECTOR OF QUALITY

Irvine, CA · On-site

$135K - $160K/yr

We have an open position for a Director of Quality located in Irvine, California facility to ... Oversight of Quality Control laboratory * Ensure that cGMP requirements and quality standards are ...

BSA Health System

Director of Quality

Amarillo, TX

Overview Join our team as a day shift, full-time, Director of Quality & Patient Safety in Amarillo ... Certification in Infection Control (CIC) required or obtained within 12 months of hire. * 5-7 years ...

Kanto Corporation

Director of Quality

Portland, OR · On-site

$160K - $190K/yr

The Role at a Glance Kanto is seeking a Director of Quality to lead our QA, QC, and QMS functions across high-purity chemical manufacturing operations. This role offers the opportunity to shape the ...

Weco Manufacturing

Director of Quality

Ontario, NY

$130K - $150K/yr

In-depth knowledge of quality control procedures and standards. * Excellent analytical and problem ... Self-directed individual with a strong sense of ownership of their work. * Results driven approach ...

VeeRteq Solutions Inc.

Director of Quality

Clifton, NJ · On-site

Director of Quality Location : Clifton, NJ Prioritized Must Have Skills for the Director of Quality: #1. Bachelor's degree in Engineering or related technical field. #2. 10+ years of progressive ...

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Director Of Quality Control information

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$31K

$125.6K

$213.5K

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

As of Jun 12, 2026, the average yearly pay for director 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.

How much does a QA director make in the US?

A Quality Assurance (QA) Director in the US typically earns between $100,000 and $160,000 annually, depending on experience, industry, and location. Senior roles with extensive experience or in high-demand sectors can exceed this range, often including bonuses and benefits.

What are the key skills and qualifications needed to thrive in the Director Of Quality Control position, and why are they important?

A Director Of Quality Control should possess a deep knowledge of quality assurance processes, regulatory standards, and industry best practices, backed by a relevant degree and substantial experience in quality management. Familiarity with quality management systems (QMS), statistical process control software, and certifications such as Six Sigma or ISO 9001 is typically expected. Strong leadership, communication, and problem-solving skills set outstanding candidates apart in this position. These competencies ensure the organization consistently meets quality standards, maintains compliance, and fosters continuous improvement.

Which is higher position, QA or QC?

In the context of a Quality Control Director, the QA (Quality Assurance) department typically holds a higher strategic role focused on preventing defects through process improvement, while QC (Quality Control) involves inspecting products to identify defects. Both functions are essential, but QA often reports to senior management and influences overall quality policies, making it generally a higher-level position within quality management structures.

What does a director of quality control do?

A director of quality control oversees the quality assurance processes within an organization, ensuring products or services meet company standards and regulatory requirements. They develop testing procedures, lead quality teams, analyze data, and implement improvements to maintain high quality levels, often using tools like quality management systems and industry certifications.

What are some common challenges a Director Of Quality Control faces in their day-to-day work?

Directors Of Quality Control often navigate challenges such as maintaining consistent quality standards across multiple teams or locations, adapting to evolving industry regulations, and effectively managing corrective actions when issues arise. They must balance the need for thorough inspections with production deadlines, while also fostering a culture of continuous improvement. Collaboration with departments like production, engineering, and supply chain is essential to resolve quality concerns and implement preventative measures. Tackling these challenges successfully helps ensure the company's products meet all necessary standards and customer expectations.

What is a Director Of Quality Control job?

A Director of Quality Control is responsible for overseeing and managing quality assurance processes within an organization. They develop and implement quality control policies, ensure compliance with industry standards, and lead teams to identify and resolve product or service issues. This role involves analyzing performance data, conducting audits, and driving continuous improvement initiatives. The director collaborates with other departments to maintain high-quality standards and ensure customer satisfaction.

Is QC a high paying job?

The salary for a Director of Quality Control is generally considered high compared to many other roles, often reflecting experience, industry, and location. These positions typically require strong leadership, technical skills, and certifications, and they tend to offer higher compensation due to their responsibility for ensuring product standards and compliance.
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Director Of Quality Control jobs near you
Infographic showing various Director Of Quality Control job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $125,600 per year, or $60.4 per hour.
Director of Quality Control

Director of Quality Control

Nivagen Pharmaceuticals

Sacramento, CA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 29 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.

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