Overview Monte Rosa Therapeutics is seeking a Senior Director Quality GCP to provide strategic oversight of phase-appropriate Quality GCP and GCLP activities, including GCP quality oversight of ongoing quality activities supporting active pre-clinical and clinical programs through participation on in-house and external cross-functional teams. This role requires an 75% on-site presence. You will work closely with industry leaders in Boston and Basel . Join a diverse, collaborative, and dynamic team that values innovation, teamwork, and a people-centric culture! Responsibilities • Primary GCP Quality contact for identified vendors and investigator sites supporting clinical programs as well as other GCP quality events (e.g., potential serious breach assessments, CAPAs) • Author key GCP quality SOPs and key reviewer for other quality (GxP) procedures. • Develop a risk-based GCP compliance program. • Support teams in the initiation, review, and closure of quality events and associated CAPA, Change Action, and Effectiveness plans. • Develop and provide GCP and other GxP training (as applicable). • Ensure appropriate qualification of vendors and ensure compliant vendor management and regular assessment/audits. May conduct GCP audits (vendors and sites). • Ensure audit observations are communicated, tracked and remediated. • Provide QA GCP review and feedback on regulatory submissions. • Lead and participate in inspection readiness activities for regulatory inspections – both internally and at clinical sites. • Interface with internal departments and external vendors on a variety of technical/quality subjects. Qualifications • BS Degree in Chemistry, Pharmacy, Biology or a related life science, or a combination of a BS Degree with relevant Quality and Technical experience. • Minimum of 16 years of experience within the pharmaceutical or biopharmaceutical industry, with development experience and exposure to commercial operations. • Knowledge and experience of clinical and commercial systems supporting GCP compliance with US and global regulations (FDA, EMA, ICH, MHRA, etc.). GLP experience a plus. • Able to provide solution-minded approach and flexibility to emerging challenges. • Able to appropriately balance priorities plus multi-task against competing priorities. • Proven experience with the desire, and ability to work in a fast-paced, matrixed, start-up environment. • Hands-on leader, able to provide solution-minded approach and flexibility to emerging challenges • Understanding of drug development and program management preferred.