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About Beeline Medicines: Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully. Job Summary: The Director, GCP Quality Assurance is responsible for providing strategic and operational Quality Assurance oversight for Good Clinical Practice (GCP) activities supporting the company’s clinical development programs. This role ensures that clinical trials are conducted in compliance with applicable regulatory requirements, company policies, and global GCP standards, with a continuous state of inspection readiness. The Director partners closely with Clinical Operations, Regulatory Affairs, Pharmacovigilance, Data Management, and external service providers to implement a risk-based quality oversight model across the clinical lifecycle. The role is accountable for GCP quality systems, vendor oversight, audits, and inspection support, and plays a critical role in embedding quality by design into clinical development programs Work Arrangement & Location:  Hybrid - This position follows a hybrid work schedule, requiring a minimum of two (2) days on-site per week — currently designated as  Tuesday and Wednesday . Additional on-site days may be required based on business needs, team priorities, or leadership direction. Essential Duties and Responsibilities: Develop and implement the GCP QA strategy aligned with clinical development objectives and global regulatory expectations Serve as a key QA partner to Clinical Operations and cross-functional stakeholders on GCP compliance and quality risk management. Promote a strong culture of quality, compliance, and continuous improvement across clinical programs Oversee GCP quality systems including deviations, investigations, CAPAs, change control, documentation, and training related to clinical activities. Ensure GCP processes are phase-appropriate, compliant, and scalable Support the development, review, and approval of GCP-related SOPs, policies, and work instructions. Provide QA oversight for GCP activities conducted internally and by CROs, vendors, and other service providers Lead GCP vendor qualification, audit strategy, and ongoing oversight using risk-based principles. Review and approve GCP-related quality agreements and vendor oversight plans Plan and execute risk-based GCP audits, including CRO audits, investigator site audits, and system audits as applicable. Lead GCP inspection readiness activities and serve as a primary QA contact during health authority inspections. Coordinate inspection preparation, conduct, and follow-up, including responses to regulatory observations. Ensure a sustainable state of inspection readiness across clinical programs. Ensure critical-to-quality considerations are embedded in clinical trial design and execution. Provide oversight of data integrity practices across GCP processes and systems. Identify, assess, and proactively mitigate GCP compliance risks Perform other duties and responsibilities as assigned Qualifications: Education: Bachelor’s degree in a scientific or related discipline; advanced degree preferred. 10+ years of experience in GCP Quality Assurance or Clinical Quality within a biotech or