Associate Director Clinical Quality Assurance Jobs in California
Associate Director Clinical Quality Assurance jobs in California are among the most active in the country, concentrated in the biopharma, medical device, and clinical research sectors that anchor the state's life sciences economy. Most hiring is in San Diego, San Francisco Bay Area, and Los Angeles, where companies like Genentech, Johnson and Johnson, and AbbVie maintain established operations. The most in-demand specialties are GCP compliance, audit management, and clinical trial quality oversight. See the openings below and apply to the ones that match your experience.
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Showing 5 of 308+ Associate Director Clinical Quality Assurance jobs
SUMMARY: The Quality Assurance Analyst I will coordinate and perform quality assurance testing of computer programs and various program output data/files; and conduct various types of analysis including workflows and processes.
Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Essential Duties and Responsibilities include the following. Other duties may be assigned.
- Works on site with consistent attendance.
- Audit exports such as CSV, Excel, flat text & 834 for accuracy
- Audit of mapping documents to source documents to system tables utilizing SQL skills
- Audit plan documents manually based upon client source documents provided by Client Managers
- Develop test plans and test cases for computer programs.
- Develop methods of regression and acceptance testing.
- Log defects and bugs.
- Validate bug fixes.
- Create checklist of sequential tasks to verify systems integrity.
- Perform testing for computer programs.
- Perform acceptance testing prior to product delivery.
- Perform regression testing prior to product delivery.
- Analyze data structure for electronic data exchange testing.
- Perform testing for electronic exchange data files.
- Establish and implement processes/workflows and develop internal documentation.
- Perform software maintenance as may be required.
- Performs other duties and responsibilities as assigned by the Management.
Supervisory Responsibilities: This job has no supervisory responsibilities.
Requirements:Knowledge, Skills, & Abilities:
- Strong understanding of accepted quality assurance standards.
- Excellent communication skills to present technical and business information to both technical and non-technical audiences.
- Strong computer skills, including Windows 10 or later, Mac OS, Word, Excel, Outlook, WinZip, SQL, Zoom and various Internet Browsers.
- Understand software development life cycle.
Education and/or Experience: High School diploma or G.E.D; and minimum of two years working in a related Information System field; or equivalent and any combination of education, training, and/or experience, which demonstrates ability to perform the duties described.
Language Skills: Ability to read, speak, and write effectively in English. Ability to interpret documents such as plan documents, memos, letters, and procedure manuals. Ability to write routine reports, meeting notes, project documentation, and correspondence. Ability to speak effectively before customers or employees of organization. Ability to effectively address or resolve customer service issues within guidelines of the position.
Reasoning and Analytical Ability:
Strong reasoning and analytical ability, including
- Ability to apply a high level of understanding and logic to interpret and carry out a variety of instructions furnished in written, oral or diagram form.
- Ability to exercise reason and logic to resolve practical problems and create effective solutions.
- Ability to analyze all relevant information and a variety of concrete variables in situations where only limited standardization exists.
- Ability to think logically and utilize analytical reasoning.
Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this Job, the employee is regularly required to sit for extended periods in front of a computer. The employee is frequently required to reach with hands and arms and talk or hear. The employee is occasionally required to stand; walk and use hands to finger, handle, or feel. The employee may frequently lift and/or move up to 10 pounds. Specific vision abilities required by this job include close vision, distance vision, peripheral vision, depth perception and ability to adjust focus. This position requires the employee to work in the office.
Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
The noise level in the work environment is usually moderate.
SUMMARY: The Quality Assurance Analyst I will coordinate and perform quality assurance testing of computer programs and various program output data/files; and conduct various types of analysis including workflows and processes.
Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Essential Duties and Responsibilities include the following. Other duties may be assigned.
- Works on site with consistent attendance.
- Audit exports such as CSV, Excel, flat text & 834 for accuracy
- Audit of mapping documents to source documents to system tables utilizing SQL skills
- Audit plan documents manually based upon client source documents provided by Client Managers
- Develop test plans and test cases for computer programs.
- Develop methods of regression and acceptance testing.
- Log defects and bugs.
- Validate bug fixes.
- Create checklist of sequential tasks to verify systems integrity.
- Perform testing for computer programs.
- Perform acceptance testing prior to product delivery.
- Perform regression testing prior to product delivery.
- Analyze data structure for electronic data exchange testing.
- Perform testing for electronic exchange data files.
- Establish and implement processes/workflows and develop internal documentation.
- Perform software maintenance as may be required.
- Performs other duties and responsibilities as assigned by the Management.
Supervisory Responsibilities: This job has no supervisory responsibilities.
Requirements:Knowledge, Skills, & Abilities:
- Strong understanding of accepted quality assurance standards.
- Excellent communication skills to present technical and business information to both technical and non-technical audiences.
- Strong computer skills, including Windows 10 or later, Mac OS, Word, Excel, Outlook, WinZip, SQL, Zoom and various Internet Browsers.
- Understand software development life cycle.
Education and/or Experience: High School diploma or G.E.D; and minimum of two years working in a related Information System field; or equivalent and any combination of education, training, and/or experience, which demonstrates ability to perform the duties described.
Language Skills: Ability to read, speak, and write effectively in English. Ability to interpret documents such as plan documents, memos, letters, and procedure manuals. Ability to write routine reports, meeting notes, project documentation, and correspondence. Ability to speak effectively before customers or employees of organization. Ability to effectively address or resolve customer service issues within guidelines of the position.
Reasoning and Analytical Ability:
Strong reasoning and analytical ability, including
- Ability to apply a high level of understanding and logic to interpret and carry out a variety of instructions furnished in written, oral or diagram form.
- Ability to exercise reason and logic to resolve practical problems and create effective solutions.
- Ability to analyze all relevant information and a variety of concrete variables in situations where only limited standardization exists.
- Ability to think logically and utilize analytical reasoning.
Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this Job, the employee is regularly required to sit for extended periods in front of a computer. The employee is frequently required to reach with hands and arms and talk or hear. The employee is occasionally required to stand; walk and use hands to finger, handle, or feel. The employee may frequently lift and/or move up to 10 pounds. Specific vision abilities required by this job include close vision, distance vision, peripheral vision, depth perception and ability to adjust focus. This position requires the employee to work in the office.
Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
The noise level in the work environment is usually moderate.
See All 308+ Associate Director Clinical Quality Assurance Jobs in California
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Find JobsAssociate Director Clinical Quality Assurance Jobs by City in California
Where California roles are concentrated, by current openings.
Associate Director Clinical Quality Assurance Job Market in California
A snapshot from current California openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Biotechnology & Pharmaceuticals12
- Technology & Software10
- Aerospace & Defense9
- Manufacturing6
- Healthcare & Medical Services6
What California Employers Look For
The qualifications that appear most often in associate director clinical quality assurance jobs across California.
- Bachelor's degree in life sciences, pharmacy, or a related field is required
- Minimum of eight years of clinical quality assurance experience in regulated environments
- Deep knowledge of FDA regulations, ICH guidelines, and GCP standards
- Proven experience leading internal and external GCP audits and inspection readiness
- Strong background managing cross-functional quality teams and CRO oversight
- Proficiency with quality management systems such as Veeva Vault or similar platforms
Associate Director Clinical Quality Assurance Jobs in California: Frequently Asked Questions
How do you become a associate director clinical quality assurance in California?
The most direct path is a bachelor's degree in a life sciences field followed by progressive clinical quality assurance experience in a regulated California biotech, pharmaceutical, or medical device environment. California does not require a state-issued license for this role, but employers consistently expect demonstrated GCP audit experience, familiarity with FDA inspection processes, and a record of managing quality teams in an IND or NDA-stage development setting.
Which companies hire associate director clinical quality assurances in California?
Companies currently hiring associate director clinical quality assurances in California include NVIDIA, Gilead Sciences, and Joby Aviation, per current listings on Migrate Mate as of July 2026. California's dense concentration of biopharma and medical device headquarters means openings appear at both global enterprise companies and well-funded mid-stage biotech firms.
Which California cities have the most associate director clinical quality assurance jobs?
San Diego, Los Angeles, and San Francisco have the most associate director clinical quality assurance openings in California. San Diego and the Bay Area lead because they host the largest clusters of biopharma and biotech headquarters and research campuses, while Los Angeles draws openings from medical device companies and contract research organizations with Southern California operations.
Are there remote associate director clinical quality assurance jobs in California?
Yes, and they are more common than in many clinical roles, since much of the work centers on document review, audit management, and regulatory oversight rather than hands-on lab activity. About 20% of associate director clinical quality assurance openings tied to California are remote or hybrid as of July 2026, with remote arrangements most typical for audit coordination, SOP development, and CRO oversight responsibilities.
How can I get hired as a associate director clinical quality assurance in California with little or no experience?
The most realistic entry point is a quality assurance associate or clinical quality specialist role at a California biotech or CRO, where you can build direct GCP audit and inspection readiness experience. Large California employers like Gilead, Genentech, and major CROs regularly hire quality coordinators and specialists as development-track positions. Earning a credential such as a Certified Quality Auditor designation strengthens your profile when moving toward director-level consideration.
Where can I find and apply to associate director clinical quality assurance jobs in California?
You can find and apply to associate director clinical quality assurance jobs in California on Migrate Mate, which lists current California openings. Search the roles that fit your background and apply directly to the ones that match your experience and target location.
See All 308+ Associate Director Clinical Quality Assurance Jobs in California
Find roles in California that match your experience and apply in just a few clicks.
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