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Associate Director Supply Chain Planning - Waltham, United States - Dyne Therapeutics Inc
Description
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 objectives
Maintain an understanding of external manufacturing site capacities, capabilities, and supply risks
Optimize supply chain processes and drive efficiency
Scenario planning of demand and supply assumptions as we drive to commercialization
Lead 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 process
Perform analysis of Dyne portfolio, including inventory projection, supply performance and risks
Integrate 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 instructions
Work within Interactive Response Technology(s) to verify and adjust clinical site and depot inventories
Manage relationships with third-party suppliers and vendors to ensure timely delivery of materials and components
Implement risk mitigation strategies to address supply chain processes and streamline operations
Ensure 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 company
Ability to effectively plan, prioritize, execute, follow up and anticipate challenges
Experience managing complex schedules and priorities in dynamic pharmaceutical, biotech or related environments
Ability to work, influence, and gain agreement across multiple functions (Manufacturing, Quality and CMC)
Strong analytical, problem solving and critical thinking skills
Strong knowledge of supply chain best practices, inventory management, and demand forecasting
Expertise 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 solutions
Excellent interpersonal, verbal, and written communication skills
Advanced analytical and problem-solving skills
Experience in working with CMC Teams
Experience in supply chain, drug development, project management, and/or pharmaceutical manufacturing/packaging
In-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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