Replimune Group, Inc. is seeking a Director of R&D Quality- Pharmacovigilance & Medical Affairs to lead QA systems for clinical safety, PV activities, and medical affairs.
You will ensure GCP/GVP compliance across global affiliates and support inspection readiness, risk mitigation, and data integrity. The role requires 10–15 years of PV/MA quality experience, strong regulatory knowledge, and proven leadership in a matrix environment.
#J-18808-LjbffrDirector, R&D Quality & PV Compliance in framingham at Unknown Company
This position is listed as full time and onsite.