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Sr. Manager, QA

Job in San Diego, San Diego County, California, 92189, USA
Listing for: Initial Therapeutics, Inc.
Full Time position
Listed on 2026-06-24
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 160000 - 186000 USD Yearly USD 160000.00 186000.00 YEAR
Job Description & How to Apply Below

SUMMARY

The Senior Manager, Quality Assurance leads the execution, maintenance, and ongoing improvement of GxP quality systems and teams that support Phase 2a through Phase 3 clinical and manufacturing operations. The role ensures compliance with GMP, GCP, and GLP requirements through direct oversight of key QA processes, including document control, training, supplier quality, deviations/CAPA, and batch disposition. This is a hybrid “player-coach” position that combines hands‑on individual contributor responsibilities with leadership of junior quality team members, including performance management, strategy, and administrative oversight.

DUTIES

AND RESPONSIBILITIES
  • Establish and execute operational objectives and work plans for GxP quality systems aligned with organizational and program priorities
  • Contribute to the development, implementation, and continuous improvement of QA policies, procedures, and standards affecting clinical and manufacturing operations
  • Drive optimization and scalability of quality systems to support late‑stage clinical development and commercial readiness
  • Manage and continuously improve multiple QA functional areas, including document control, training systems, supplier quality, quality events (deviations, CAPA, change control, nonconformance), and batch disposition
  • Ensure compliant and timely execution of core QMS processes, including investigation closure, documentation accuracy, and adherence to regulatory expectations
  • Establish and monitor quality metrics, trends, and reporting to assess system effectiveness and identify risks
  • Lead and coordinate inspection readiness activities, ensuring ongoing audit preparedness across quality systems and operations
  • Oversee internal, external, and regulatory audit activities, including preparation, execution, and timely resolution of findings
  • Ensure appropriate identification, escalation, and mitigation of quality and compliance risks with potential operational or regulatory impact
  • Partner cross‑functionally with Clinical Operations, Manufacturing, Regulatory Affairs, and R&D to align on quality requirements and operational execution
  • Influence cross‑functional decision‑making related to quality, compliance, and risk management
  • Communicate quality system performance, risks, and priorities to senior management and key stakeholders
  • Delegate work, manage priorities, and ensure alignment of team deliverables with departmental and organizational goals
  • Foster a culture of accountability, quality, and continuous improvement across the team and broader organization
  • Lead or sponsor cross‑functional initiatives to improve quality system effectiveness and operational performance
  • Mentor junior staff and contribute to knowledge sharing across the organization
EDUCATION AND EXPERIENCE
  • Bachelor’s degree in life sciences, health sciences, or related field (advanced degree preferred)
  • Minimum 8 years of experience in the cGMP pharmaceutical or biotechnology industry; latest‑stage clinical to commercial manufacturing environments and/or stem cell manufacturing experience preferred
  • Experience with electronic QMS and/or electronic batch record (E ) systems is a plus
  • Minimum 5 years of experience in conducting internal and external audits;
    Certified Quality Auditor (CQA) or equivalent preferred
  • Minimum 5 years of direct people management or supervisory experience
JOB SPECIFICATIONS
  • Quality Systems Leadership: Ability to design, optimize, and scale core QMS processes to ensure compliance, efficiency, and long‑term sustainability
  • Regulatory Expertise: Advanced knowledge of GMP, GCP, GLP, and global regulatory frameworks (FDA, EMA, ICH) and their practical application
  • Strategic Execution: Ability to translate functional strategies into operational plans, priorities, and measurable outcomes
  • Risk Assessment: Strong capability to apply risk‑based decision‑making to identify, evaluate, and mitigate compliance and operational risks
  • Cross‑Functional Influence: Ability to align stakeholders, drive decisions, and influence outcomes across multiple functional areas
  • People Leadership: Proven ability to build, develop, and lead high‑performing teams through coaching, accountability, and…
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