Cmc Project Manager Jobs in Madison, WI (NOW HIRING)

The Position

The Group Manager, PDO is a member of a team charged with ownership of end-to-end alignment of Arrowhead products from preclinical through commercial phases. This role is accountable for assigned projects and provides leadership to cross-functional CMC teams from drug substance process development through delivery of clinical kits. This role oversees both internal and external CMC activities to ensure alignment with program timelines, quality standards, and regulatory requirements. The position will have direct reports and is responsible for mentoring, performance management, and team development. In addition, this individual is partner-facing, serving as a key point of contact for stakeholders and external partners. The role will manage external relationships, including partnerships, and act as the primary contact for contract manufacturing organizations (CMOs) and contract research organizations (CROs) supporting development, analysis, manufacturing, packaging, and labeling activities for Arrowhead drug development programs.

Responsibilities

• Act as primary point of contact for projects, facilitating communication between internal and external team members for CMC development, analytical, manufacturing, packaging, and labeling activities with minimal support of direct management
• Maintain a clear understanding of project status and tailor communications appropriately for Arrowhead leadership, relevant stakeholders, and partner companies
• Manage budget, timeline, quality and deliverables for each project and vendor
• Escalate risks, drive scenario planning, and present recommendations to leadership teams
• Maintain and expand upon current project tracking tools (ex. Smartsheet, Excel, Power BI)
• Analyze project metrics and prepare recommendations for leadership
• Interface with cross-functional project team (Chemistry, Engineering, Analytical, Quality) on partner development and manufacturing activities
• Track, manage, and negotiate new proposals and draft RFPs with support from technical SME's and Legal
• Steer alignment among technical SME's, Sourcing & Supplier Management, Legal, and Finance on contracts, supply agreements, confidentiality agreements, and purchase orders for new and existing vendors
• Track vendor invoices and collaborate with Finance to process payments
• Develop, collect, and maintain performance metrics for internal and external partners
• Lead project meetings, vendor/partner visits, and conference calls
• Facilitate internal discussions to obtain team consensus and decisions
• Drive business review meetings with vendors with support from Sourcing & Supplier Management
• Support vendor management responsibilities and activities, as needed
• Assist in developing and review CMC outsourcing budget
• Coach and mentor direct reports in the creation of personal goals, development, and performance improvement
• Generate, maintain, and approve training materials and support onboarding of new team members
• Collaborate with Alliance Management on partnership goals.
• Other duties as assigned

 Requirements

• Bachelor's degree in a scientific field such as Chemistry, Chemical Engineering, Biochemistry, Biotechnology
• Eight years of increasing responsibility in a pharmaceutical company, contract manufacturing organization or contract research organization including direct report experience
• Minimum five years in a project management role with experience managing clients, partners, and/or vendors
• Knowledge of applicable GLP, GMP, and regulatory guidance for pharmaceutical manufacturing and testing
• Strong MS Office skills (Outlook, Excel, PowerPoint, and Word)
• Excellent verbal and written communication skills
• Ability to work with diverse professionals in a matrix environment
• Highly motivated team player willing to contribute to a growing biotech organization
• A detail oriented, organized, self-starter who endeavors to anticipate problems and seeks opportunities to grow the role and responsibilities at Arrowhead

Preferred

• Master's degree in Chemistry, Chemical Engineering, Biochemistry or related science field
• GLP or GMP Laboratory or Manufacturing experience
• Experience with late-stage CMC drug development and commercialization activities
• Project Management Certification
• ERP system experience