More jobs:
Sr. Manager, QA
Job in
San Diego, San Diego County, California, 92189, USA
Listed on 2026-06-24
Listing for:
Initial Therapeutics, Inc.
Full Time
position Listed on 2026-06-24
Job specializations:
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist
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.
DUTIESAND 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
- 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
- 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…
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
Search for further Jobs Here:
×