ZipRecruiter

Log In

1

Associate Director Quality Control Jobs in California

Socket.dev

Director, QC & Microbiology

San Diego, CA · On-site

The Director, QC & Microbiology provides strategic and operational leadership for the site's Quality Control Chemistry and Microbiology functions, ensuring scientific excellence, regulatory ...

Revance

Executive Director, Quality Control

Newark, CA · On-site

Job Summary The Executive Director of Quality Control will be responsible for all aspects of quality control from drug development through commercialization, including the manufacture of clinical ...

Baxter Healthcare

Associate Director, Quality

Hayward, CA · On-site

$160K - $220K/yr

Direct large-scale programs and departmental initiatives in support of division-wide and company-wide objectives. * Maintain accountability for product quality, regulatory compliance, and adherence ...

Baxter

Associate Director, Quality

Hayward, CA · On-site

$160K - $220K/yr

Direct large-scale programs and departmental initiatives in support of division-wide and company-wide objectives. * Maintain accountability for product quality, regulatory compliance, and adherence ...

previous pagenext page

Showing results 21-40

All JobsAssociate Quality Control JobsAssociate Director Quality Control JobsAssociate Director Quality Control Jobs in California

Associate Director Quality Control information

What is an associate director quality control?

An Associate Director of Quality Control is a senior management professional responsible for overseeing the quality control processes within an organization, often in industries like pharmaceuticals, biotechnology, or manufacturing. They lead teams that test and monitor product quality, ensure compliance with regulatory standards, and develop strategies to improve testing procedures. Their role involves managing budgets, mentoring staff, and collaborating with other departments to uphold product integrity. Associate Directors of Quality Control often report to higher-level executives and play a key role in maintaining customer trust and regulatory approval.

What are the key skills and qualifications needed to thrive as an associate director quality control?

To thrive as an Associate Director of Quality Control, you need in-depth knowledge of quality management systems, regulatory compliance, and relevant scientific or technical expertise, typically supported by a degree in life sciences or engineering. Familiarity with laboratory information management systems (LIMS), quality assurance software, and certifications such as Six Sigma or ASQ are highly valuable. Leadership, problem-solving, and strong communication skills help drive team performance and foster cross-functional collaboration. These skills ensure rigorous product quality, regulatory adherence, and operational efficiency in quality-driven environments.

What are the main challenges an associate director quality control typically faces when managing a diverse QC team?

An Associate Director of Quality Control often manages teams with varied technical backgrounds, which can lead to challenges in aligning processes, maintaining consistent training standards, and ensuring clear communication across functions. Balancing the demands of regulatory compliance, tight production timelines, and continuous improvement initiatives is also a common challenge. Successful leaders in this role foster a culture of collaboration, prioritize ongoing training, and implement standardized procedures to help their teams deliver reliable results and support broader organizational goals.

What is the difference between Associate Director Quality Control vs Quality Control Manager?

AspectAssociate Director Quality ControlQuality Control Manager
CredentialsBachelor's/Master's in Life Sciences, Quality Certifications (e.g., CQE)Bachelor's/Master's in Life Sciences, Quality Certifications (e.g., CQE)
Work EnvironmentLeadership role in labs or manufacturing facilities, overseeing teamsSupervises QC teams, conducts testing, and ensures compliance
Industry UsageUsed in pharmaceutical, biotech, and biotech manufacturing companiesCommon in similar industries, often reporting to Associate Directors

The Associate Director Quality Control typically holds a higher strategic and leadership role, overseeing multiple teams and ensuring compliance at a broader level. The Quality Control Manager focuses more on daily testing, team supervision, and operational tasks. Both roles require similar credentials but differ in scope and responsibility.

What are popular job titles related to Associate Director Quality Control jobs in California?

For Associate Director Quality Control jobs in California, the most frequently searched job titles are:

What job categories do people searching Associate Director Quality Control jobs in California look for?

The top searched job categories for Associate Director Quality Control jobs in California are:

What cities in California are hiring for Associate Director Quality Control jobs?

Cities in California with the most Associate Director Quality Control job openings:

Infographic showing various Associate Director Quality Control job openings in California as of September 2026, with employment types broken down into 2% As Needed, 78% Full Time, 16% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 83% Physical, 1% Hybrid, and 16% Remote job distribution.

Associate II, Quality Control Biology (Temporary)

San Diego, CA • On-site

Artiva Biotherapeutics, Inc.
Biotechnology Research and Development • 11 - 50 employees
Learn more about Artiva Biotherapeutics, Inc.external

Temporary

Posted 29 days ago

Job description

About Artiva:

We are a clinical-stage biotechnology company focused on developing natural killer (NK) cell-based therapies. Our mission is to develop effective, safe, and accessible cell therapies for patients with devastating autoimmune diseases. We aim to develop therapies that patients and physicians can utilize in a community setting. Our lead product candidate,AlloNK, is a non-genetically modified, cryopreserved NK cell therapy being evaluated in combination with B-cell targeted monoclonal antibodies (mAbs). We believe the compelling cell killing properties of NK cells, when combined with mAbs for targeting, creates an opportunity to generate potentially transformative therapies.


For more information, visit
www.artivabio.com.


Job Summary:

Artiva Biotherapeutics is seeking a skilled and motived QC Associate II, QC Biology (Temporary) who will be reporting to the Associate Director, Quality Control. This individual will perform routine cGMP release and stability testing of Artiva's NK cell therapy products, support laboratory investigations, and contribute to continuous improvement of QC systems. The contract will be through the end of the year with possible extension beyond that.

Duties/Responsibilities:

  • Assist in ordering supplies, reagents and equipment.
  • Write and revise SOPs/Test methods that support Artiva's cell therapy products.
  • Operate and test ELISA, Flow Cytometers, automated cell counters, and other analytical instruments and equipment, as needed.
  • Support activities for QC equipment IQ/OQ/PQs.
  • Perform routine cGMP release and stability testing of Artiva's products; including biological tests, biochemistry, chemistry-based tests as needed.
  • Support and as needed evaluate QC systems and/or implement system improvements with supervision.
  • Support laboratory investigations and write reports for deviations and Out of Specification results.
  • Document lab work in a thorough and accurate manner.
  • Perform all work according to company policies, SOPs, and cGMP practices.
  • Assist in planning for GMP release testing, including testing schedules, reviewing biology data and investigating OOS and OOT results.
  • Write technical QC protocols and reports as needed.
  • Assist in analytical qualification and validation, as necessary.
  • Support the transfer and optimization of analytical methods from Analytical Development (or contract laboratories).
  • Develop an in-depth understanding of NK products, testing, and safety.
  • Maintain records and databases in accordance with procedures.
  • Support other special QC projects as needed.

Qualifications:

  • Bachelor's degree (BS/BA) or relevant scientific field, preferably in biology or related field.
  • Minimum 2 years of cGMP QC experience in a cell therapy/biotech/pharmaceutical setting is required.
  • Knowledge and experience in supporting cGMP deviations, OOS, etc.
  • Basic knowledge of method transfers, qualifications, and validations; current industry practices; and some experience with guidance interpretation and application
  • Adept at learning critical thinking and technical writing skills.
  • Computer skills required to operate Microsoft Word and Excel programs.

Base Salary: $ 74,000 - $ 85,000. Exact compensation may vary based on level, skills and experience.

Apply