Associate Project Management

Note:Fully Remote roleWork Schedule: DayshiftThe *** Contract Development and Manufacturing (ACDM) organization is seeking a highly qualified candidate to support synthetic-related outsourcing associated with execution of external development, commercial and clinical supply of drug substance (DS). The position will be focused on synthetic small molecule drug substance/process chemistry and serve as a key enabling role in a high-performing cross-functional organization. Individual projects may span development, sourcing (e.g., requests for proposal and site selection), supplier onboarding, manufacturing, and continuous improvement activities for both non-GMP and GMP commercial / clinical deliverables.The *** Contract Development and Manufacturing team develops and implements the external sourcing strategy for *** s portfolio from early phase through commercial delivery. This role will support engagement and oversight of *** Contract Development and Manufacturing sites through executing activities according to Good Manufacturing Practices (cGMP) principles and the ACDM business practices.Job Responsibilities:Day-to-day oversight for external synthetic/process chemistry-related projects:Overseeing and supporting ongoing activities at selected sites along with any subcontracted sites to ensure project deliverables, including compliance, timelines, product quality, and costWorking closely with the ACDM team, Process Development, External Quality, Supply Chain, and other internal stakeholders to support sourcing activities, including managing scope of work (SoW) and quotation request documentsCoordinating requests for shipment of materials/samples between sitesManaging purchase orders, invoices, and project-related budgetOverseeing deviations investigations and change managements as neededMaintain and update business related trackers as neededSupport continuous improvement projects and operational excellence within ACDMPerforming other related duties and tasks as necessary or as assignedBasic Qualifications:- Bachelor's Degree in Engineering, Chemistry, or Science-related field- 4+ years of Manufacturing or Operations experiencePreferred Qualifications:Knowledge of synthetic drug development and manufactureExperience in Project ManagementUnderstanding of cGMP, Operations and Regulatory/CMC policies and requirements, especially in the Pharmaceutical IndustryExperience with interfacing and managing CRO and CDMO relationshipsExperience with change management, deviation investigations and implementation of corrective/preventive actionsUnderstanding of tech transfer, drug development and commercialization of synthetic therapeuticsExperience working in cross-functional settings, as part of cross-functional team or matrix teamStrong interpersonal relationship and communication skills both written and verbal