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Director Quality Control Jobs in California (NOW HIRING)

PCI Pharma Services

Director, QC

San Diego, CA

The role oversees QC Chemistry, Method Transfers,Stability, Raw Materials, and Logistics operations supporting GMP manufacturing, release testing,investigations, and regulatory compliance. This ...

PCI Pharma Services

Director, QC

San Diego, CA · On-site

The role oversees QC Chemistry, Method Transfers, Stability, Raw Materials, and Logistics operations supporting GMP manufacturing, release testing, investigations, and regulatory compliance. This ...

Moderna Therapeutics

The Role The Associate Director, Quality Control Lab Automation Strategy & Digital Integration is responsible for leading the strategy, implementation, and lifecycle management of laboratory ...

NCSL International

QC DIRECTOR

Rocklin, CA · On-site

$180 - $240/hr

CPC is seeking a Director of Quality Control (QC) to fill a full‑time, on‑site role in our Rocklin, California facility. This position will report directly to either the CEO or QA Director and is ...

New

YQN

Quality Control Director

Fontana, CA · On-site

$130K/yr

The Quality Control Director is responsible for establishing, optimizing, and overseeing the end-to-end quality assurance framework across all warehouse locations nationwide. This role leads quality ...

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Director Quality Control information

See California salary details

$30.6K

$124K

$210.7K

How much do director quality control jobs pay per year?

As of Aug 7, 2026, the average yearly pay for director quality control in California is $123,956.00, according to ZipRecruiter salary data. Most workers in this role earn between $89,800.00 and $149,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a director quality control, and why are they important?

To thrive as a Director of Quality Control, you need deep expertise in quality assurance methodologies, regulatory compliance, and management, typically supported by a degree in science or engineering and substantial industry experience. Familiarity with quality management systems (QMS) like ISO 9001, Six Sigma certification, and proficiency in data analysis tools are often required. Strong leadership, problem-solving abilities, and effective communication skills help drive cross-functional collaboration and continuous improvement. These competencies ensure product quality, regulatory adherence, and operational excellence in highly regulated industries.

What are some common challenges faced by a director quality control, and how can they be addressed?

Directors of Quality Control often encounter challenges such as maintaining compliance with evolving regulatory standards, managing cross-functional teams, and ensuring consistent product quality across multiple locations. To address these challenges, it's important to stay updated on industry regulations, foster open communication between departments, and implement robust training and quality management systems. Regular audits, data-driven decision making, and strong leadership are also key to overcoming obstacles and ensuring continuous improvement within quality control operations.
What are the most commonly searched types of Quality Control jobs in California? The most popular types of Quality Control jobs in California are:
What cities in California are hiring for Director Quality Control jobs? Cities in California with the most Director Quality Control job openings:
Director Quality Control jobs near you
Infographic showing various Director Quality Control job openings in California as of August 2026, with employment types broken down into 1% As Needed, 71% Full Time, 22% Part Time, 2% Temporary, 3% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $123,956 per year, or $59.6 per hour.

Director, Quality Control

Corcept Therapeutics

Redwood City, CA

$215K - $253K/yr

Full-time

Re-posted 29 days ago

Job description

The position will provide strategic and organizational leadership for the Quality Control function supporting Corcept's development and commercial programs. This position will have end-to-end oversight of all stability programs at contract laboratories and will author the stability sections of regulatory filings. This position will partner closely with the Sr Director of Analytical Development & Quality Control (ADQC) to continuously strengthen, expand, and scale the QC function, with increasing responsibility across broader QC activities.  

Responsibilities:

  • Lead the QC function with primary responsibility for the design, execution, and oversight of stability programs
  • Oversee stability studies conducted at external laboratories, ensuring compliance, data integrity, and timely execution
  • Review, trend, and maintain stability data. Alert the project team of any adverse trending
  • Collaborate with vendors and internal cross-functional teams to ensure that out-of-trend and out-of-specification results are addressed promptly
  • Provide stability study progress summaries to project teams and ensure that stability reports are completed promptly
  • Oversee internal documentation to support retest periods and shelf-life extension based on data generated from ongoing stability studies
  • Support analytical project leads in preparation of batch analysis; author and review stability sections required for regulatory submissions
  • Support analytical project leads in reviewing method validation protocols, reports, analytical method and test data
  • Manage data review qualifications of contract laboratories
  • Partner with the Sr Director of ADQC to build and enhance QC capabilities, infrastructure, and processes, with the expectation to progressively expand scope into broader QC oversight

Preferred Skills, Qualifications or Technical Proficiencies:

  • Strong technical expertise in stability study design, execution, and interpretation
  • Proven experience managing stability programs supporting late-stage development and global regulatory submissions
  • Experience in managing analytical testing in an outsourced environment
  • Experience in using statistical tools for data trend analysis and projection of drug substance retest period or drug product shelf-life
  • Excellent communication and collaboration skills with proven ability to work effectively with other functional groups

Preferred Education and Experience:

  • S. in relevant scientific discipline. Advanced degree in Analytical Chemistry or other relevant disciplines
  • 10+ years QC experience in the pharmaceutical industry

The pay range that the Company reasonably expects to pay for this headquarters-based position is $215,300-$253,200; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.

 Applicants must be currently authorized to work in the United States on a full-time basis.

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