DirectorSenior Director, Quality Assurance

Job Title: Director/Senior Director Quality Assurance

Department: Quality
Reports to: CEO
Location: Onsite 2-3 days/week Berkeley CA
Employment Type: Full-Time
FLSA Status: Exempt
Bonus/Equity: Eligible

About Azalea

Azalea Therapeutics is enabling precision genome engineering directly inside the body with an initial focus on creating cancer immunotherapies in vivo . Azalea is pioneering a new way to turn a persons own T cells into a powerful cancer therapy directly inside the body. Instead of removing cells and manipulating them in a lab we use precision genome editing tools to engineer T cells where they already live. At the center of our approach are Enveloped Delivery Vehicles or EDVs. As highly selective couriers EDVs are designed to specifically locate T cells within the patient and deliver our genome engineering cargo. Once inside the cell the anti-cancer agent is inserted into a precise site in the genome ensuring safe and potent modifications to fortify the T cells against cancers.

Why this matters:

• We aim to make cell therapy faster and more accessible by avoiding complex manufacturing outside the body.
• Our platform is designed for precision so the right cells are safely programmed to effectively fight cancer.
• This technology has the potential to treat a wide range of cancers with a streamlined scalable process.

Our goal is simple: develop next-generation delivery technologies to bring genetic engineering and cell therapies to more patients.

How We Work

Azalea is building ambitious science in a fast-moving environment. The people who thrive here are accountable adaptable rigorous humble and direct. Across roles and functions we look for team members who demonstrate the following:

• Outcome Ownership - We own results close loops and follow through without needing to be prompted. We take responsibility for moving work forward and making sure important decisions deliverables and handoffs do not fall through the cracks.
• Comfort with Ambiguity - We operate in an early-stage environment where information may be incomplete and priorities may evolve. We clarify quickly make thoughtful decisions with the information available and adapt without unnecessary drama.
• High Standards Low Ego - We care deeply about the quality of the work and the impact it can have for patients. We raise the bar while staying humble direct and open to feedback.
• Collaboration and Candor - We share context early communicate clearly partner across functions and operate with transparency. We believe strong collaboration requires both trust and direct communication.

The Opportunity

The Director/Senior Director Quality Assurance will be Azaleas first dedicated Quality Assurance hire and will build the QA function required to support external manufacturing GMP readiness regulatory interactions and future clinical supply.

This is a hands-on leadership role for a Quality Assurance leader who can establish phase-appropriate and right-sized systems in an early-stage company while maintaining rigorous standards for patient safety data integrity and regulatory compliance. The role will partner closely with CMC Process Development Analytical Development Regulatory Affairs Clinical and CDMO partners and consultants to advance AZA-2509 and pipeline programs toward first-in-human clinical development.

Key Responsibilities

• Build and lead Azaleas Quality Assurance function including the quality strategy operating model roadmap and resourcing plan appropriate for an early-stage biotechnology company advancing toward first-in-human studies.
• Establish implement and continuously improve a phase-appropriate Quality Management System including SOPs document control training deviation and CAPA management change control risk management vendor qualification batch record review product disposition audits complaints and quality metrics.
• Serve as the QA business partner to CMC Process Development Analytical Development External Manufacturing Regulatory Affairs Clinical and Program Team leaders to ensure quality considerations are embedded into program planning and execution.
• Lead QA oversight of external co nsultants CDMOs testing laboratories and other GxP vendors including quality agreements vendor qualification audit planning issue escalation and ongoing performance management.
• Establish and execute batch release and disposition processes for development engineering GMP and future clinical materials including review of batch records deviations investigations analytical data packages certificates of analysis and supporting documentation.
• Provide QA leadership for EDV and AAV manufacturing and analytics including phase-appropriate controls for process development analytical method development pilot runs engineering runs and GMP manufacturing readiness.
• Define and maintain quality requirements for labeling packaging and clinical supply documentation including awareness of requirements that may apply inside and outside the United States.
• Support regulatory strategy and submissions by contributing quality content reviewing CMC documentation preparing for health authority interactions and ensuring commitments are tracked and closed.
• Prepare the organization and work with external partners for audits and inspections by establishing inspection readiness practices maintaining traceable documentation and leading response planning for quality observations.
• Develop practical quality risk management approaches that help Azalea make sound decisions in an early-stage environment while protecting patient safety product quality and data integrity.
• Translate quality strategy into clear priorities accountabilities and decision points; close loops on issues that cross internal functions and external partners.
• As the function grows recruit develop and lead QA team members and consultants setting expectations for high standards direct communication and accountable follow-through.

Qualifications

Minimum Qualifications

• 10 years of progressive Quality Assurance leadership experience in biotechnology biologics cell therapy gene therapy or another complex modality with manufacturing and external partner oversight.
• Demonstrated experience partnering with CDMOs and external testing laboratories in a GMP environment.
• Proven track record establishing and scaling quality systems SOPs quality agreements vendor oversight practices and batch release processes in a biotechnology setting.
• Hands-on experience with product batch record review deviation assessment CAPA change control product disposition and release documentation.
• Strong working knowledge of applicable GxP expectations and relevant U.S. and international Quality requirements for investigational products clinical supply labeling documentation and external manufacturing oversight.
• Experience supporting regulatory submissions health authority interactions audits and inspection readiness activities.
• Ability to operate as both a strategic function builder and a hands-on executor in an early-stage company environment.
• Strong cross-functional leadership skills including the ability to influence senior stakeholders drive alignment and make clear recommendations when information is incomplete.
• Bachelors degree in life sciences engineering quality or a related discipline or an equivalent combination of education and relevant experience.

Preferred Qualifications

• Experience in cell therapy gene therapy in vivo genome editing AAV viral vectors biologics or other advanced therapy medicinal products.
• Experience as the first or early Quality hire in a start-up or small biotechnology company.
• Experience building a QA organization from the ground up including use of consultants and external specialists before full internal teams are in place.
• Experience supporting first-in-human readiness pre-IND preparation or early clinical development programs.

What Success Looks Like (first 36 months)

• Assess Azaleas current quality systems external partner oversight and overall GMP readiness. Translate findings into a practical QA roadmap aligned with first-in-human priorities.
• Establish or advance the highest-priority elements of a phase-appropriate QMS including document control training deviation/CAPA change control vendor qualification audit planning and quality metrics.
• Build effective QA partnerships with CMC Process Development Analytical Development Regulatory Affairs Clinical and external CDMO/testing partners to clarify expectations close gaps and strengthen execution.
• Establish foundational batch review product disposition quality agreement and vendor oversight processes for development engineering GMP and future clinical materials.

Working Conditions / Physical Requirements

• Onsite 2-3 days per week in our Berkeley office
• Travel up to 25%

Compensation and Benefits

• The expected salary range for this role based on the primary location for this position in California is $185000 - $260000 per year. Offer amounts are determined by factors such as experience qualifications geographic location and other job-related factors permitted by law. Salary will be commensurate with experience qualifications training and market.
• This role is eligible for annual performance bonuses equity grants and a comprehensive benefits package that includes medical dental vision retirement plan with company match and paid time off.

Azaleas Commitments

Equal Employment Opportunity (EEO): Azalea is an equal opportunity employer. We consider qualified applicants without regard to race color religion sex gender identity or expression sexual orientation national origin ancestry age disability medical condition genetic information marital status military or veteran status or any other characteristic protected by applicable law.

Reasonable Accommodation: We will provide reasonable accommodation to qualified individuals with disabilities and to individuals with sincerely held religious beliefs consistent with applicable law. To request accommodation email HR at HR email.

Applicant Privacy: Azalea collects and uses applicant personal information for recruiting and employment purposes. If applicable Azalea will provide a California applicant privacy notice describing categories of information collected purposes retention and rights under the California Consumer Privacy Act (CCPA/CPRA).

Job Description Disclaimer: This job description may change at any time based on business needs. It is not a contract and does not create a promise of employment for any particular duration.

Notice to Recruiters/Staffing Agencies: Recruiters and staffing agencies should not contact Azalea Therapeutics through this page. We require that all Recruitment Vendors (e.g. search firms recruitment agencies and staffing companies) have a fully executed formal written agreement on file with Azalea prior to submitting candidates. Any resumes submitted through the website or directly by Recruitment Vendors will be considered unsolicited. Unsolicited vendor submissions do not constitute any actual or implied contract with Azalea and Azalea will not be responsible for any purported fees. For more information please contact our HR team at

Information on Fraudulent Job Offers: Azalea is aware that some job seekers have received false employment offers or recruitment emails from individuals or organizations posing as Azalea. The individuals or organizations sending these false employment offers may send requests seeking to gain personal information items of value or monetary funds under the premise that doing so is required to further the recruitment process.

Azalea never requests passport details financial information items of value or money from job seekers for any reason as part of the recruitment process. Individuals who receive an offer of employment from Azalea are always required to go through a formal recruitment process which includes an interview with a member of Azaleas Human Resources recruitment team and the hiring manager.

Legitimate email communications from Azalea will also only use emails that end in @ from our core recruitment team. Fraudulent emails claiming to be sent by Azalea or Azalea employees may come from similar sounding emails with endings like @ or @ or even emails ending in common public domain addresses with endings like @ or @. There can also be instances of fraudulent communication that use the names and pictures of known company employees claiming to be sent from those employees or that even link out to fake websites that were created to look and feel like the real company website.

We are taking steps to investigate these fraudulent communications. If you feel that you have been a potential victim of an employment application scam please contact the Internet Crimes Complaint Center at . The Internet Crimes Complaint Center is an FBI entity that aggregates criminal events in order to analyze and prosecute numerous related scams.

Required Experience:

Exec