Role Summary:
The Associate Director of Supply Chain Planning is responsible for inventory planning and tracking for Dyneâs end-to-end external supply chain, maintaining a production plan that includes long range planning (LRP), ensuring continuous clinical supply, and commercial launch readiness builds and scenario planning for our assets. This role is instrumental in executing our current supply planning and in helping us develop and implement our future capabilities There role collaborates closely with Process Development, Research, CMC, and Quality Control and Quality Assurance. The person in this role is a strategic and results-driven professional with experience in collaborative supply chain planning.
This role is based in Waltham, MA without the possibility of being a remote role. Applicants must be able to relocate to the area.
Primary Responsibilities Include:
Collaborate with CMC, Logistics, Quality Control, Quality Assurance, and Clinical Operations to develop and maintain a valid demand and supply plan, ensure the availability of products for patients, and support the companyâs business objectivesMaintain an understanding of external manufacturing site capacities, capabilities, and supply risksOptimize supply chain processes and drive efficiencyScenario planning of demand and supply assumptions as we drive to commercializationLead monthly demand and supply planning meetings with cross functional team members as part of our drive to a formal Integrated Business Planning / Sales and Operations Planning processPerform analysis of Dyne portfolio, including inventory projection, supply performance and risksIntegrate with other global planning processes to monitor key performance indicators (KPIs) and analyze supply chain data to identify opportunities for improvement and cost savings (e.g. Demand, Inventory, Sales and Operations Planning process and Key Performance Indicators )Author Supply Chain-related standard operating procedures (SOPs) and work instructionsWork within Interactive Response Technology(s) to verify and adjust clinical site and depot inventoriesManage relationships with third-party suppliers and vendors to ensure timely delivery of materials and componentsImplement risk mitigation strategies to address supply chain processes and streamline operationsEnsure compliance with regulatory requirements and quality standards in supply chain operations
Education and Skills Requirements:
Bachelor’s Degree in Engineering, Supply Chain, Business or related field, or equivalent with 8+ years of related work experience in a biotechnology companyAbility to effectively plan, prioritize, execute, follow up and anticipate challengesExperience managing complex schedules and priorities in dynamic pharmaceutical, biotech or related environmentsAbility to work, influence, and gain agreement across multiple functions (Manufacturing, Quality and CMC)Strong analytical, problem solving and critical thinking skillsStrong knowledge of supply chain best practices, inventory management, and demand forecastingExpertise in use of MS Excel, as well as demonstrated proficiencies in Smartsheet, Visio, ERP systems and Power BI (or similar application)Collaborative work style to be part of a team to identify process gaps and develop solutionsExcellent interpersonal, verbal, and written communication skillsAdvanced analytical and problem-solving skillsExperience in working with CMC TeamsExperience in supply chain, drug development, project management, and/or pharmaceutical manufacturing/packagingIn-depth working knowledge of regulations relating to clinical manufacturing, packaging and distribution activities (CGMP, GCP)APICS or CSCMP certification a plus
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