Program and Alliance Manager Associate Director
Rion Inc.
Rochester, MN, USA Hybrid
Full time
Program and Alliance Manager Associate Director
Rion Inc.
Position Summary
Reporting to the VP of Program & Alliance Management, the Associate Director of Program & Alliance Management is a primary partner-facing role responsible for execution and oversight of partnered programs and partner relationships. The Associate Director will drive alignment and accountability across internal cross functional teams while fostering strong, transparent partner relationships through ownership of program execution, partner communications, scope/schedule/cost management, and proactive issue escalation, as appropriate.
Alliance Management Key Responsibilities
Partnered Program Leadership & Execution
Lead integrated joint program planning efforts
Lead program execution with minimal oversight, anticipating downstream impacts to manufacturing, quality, and regulatory deliverables, as well as commitments made to partners
Drive alignment between contractual scope and operational execution; ensure programs are executed in alignment with approved scope, schedule, and quality requirements
Lead joint internal/partner escalation discussions and provide executive-level updates
Partner Alliance & Relationship Management
Serve as a partner advocate for internal budget, resource and prioritization efforts
Build and maintain strong, trust-based relationships with partner teams and leadership
Manage partner expectations through transparent communication of risks and mitigation options and impact
Support partner satisfaction through responsiveness, consistent delivery, and issue resolution
Program Management Key Responsibilities
Internal Cross-Functional Coordination
Translate partner objectives, detailed in scopes of work (SOWs), into actionable internal workplans with clear ownership and accountability
Drive alignment across Rion internal line functions, including R&D, Analytical and Process Development, GMP Manufacturing, Supply Chain, QA, QC, Clinical, and Regulatory Affairs
Operate with a deep understanding of GMP environments, quality systems, and inspection readiness; partner with Quality to assess and communicate impacts of deviations, CAPAs, and change controls to timelines of milestone deliverables and partner commitments
Joint Program Coordination
Create a positive team environment that instills trust, ensures clear and transparent communication, and promotes alignment on program objectives and priorities
Lead routine joint internal/partner program meetings and focused ad-hoc meetings as necessary
Ensure meeting minutes, action items, and decisions are documented and tracked to closure
Develop program timelines; actively manage dependencies and constraints
Facilitate critical decision-making within the team; identify where strategic and operational adjustments are necessary throughout development
Drive issue identification and resolution, risk management and contingency planning
Prepare clear, accurate program status updates for joint team members and leadership; maintain transparency regarding risks, mitigations, options, and impact to enable efficient decision-making, and appropriately escalate as necessary
Scope Contracts, Change Control, Financial Oversight
Support development and execution of Statements of Work (SOWs) based on partner objectives and internal capabilities
Develop (with line functions) cost projections associated with SOWs; track to actual spend
Ensure alignment between execution and contractual obligations; generate change orders where necessary
Partner with Finance to track program milestone completion and invoicing readiness
Measures of Success
Strong internal collaboration and effective cross-functional coordination
Clear execution-to-contract alignment across programs
On-time, compliant delivery of partner program milestones
Clear visibility of program health, risks, and milestone delivery status
High partner satisfaction
Required Qualifications
A minimum of 10 years of biotech/pharmaceutical industry experience with at least 5 years of relevant Project Management experience
Strong leadership, negotiation, and conflict management skills; experience in managing projects and people in a team environment through change
Proven track record of successfully leading complex, multi-functional programs in GMP settings to deliverables
Demonstrated experience coordinating cross-functional teams in a regulated GMP environment.
In-depth knowledge of biological drug development process with preferred experience in late-phase and commercial programs
Strong understanding of pharmaceutical/biotech workflows, including GMP manufacturing, GMP testing, manufacturing process implementation and/or tech transfer, quality systems, clinical trial execution, and regulatory submissions
Experience in program/project management best practices and project management tools
Bachelor of Science degree in life sciences, engineering, or relevant to medicine, human disease, or pharmaceutical development
Ability to travel domestically up to 20%
Excellent communication, organization, and stakeholder relationship and management skills
Preferred Qualifications
Direct experience working in a CMO/CDMO environment managing sponsor programs strongly preferred
Experience managing late-stage development, validation/PPQ, BLA-preparedness, or commercial manufacturing programs
Familiarity with contract management, change order processes, and financial tracking
Experience with contract structures (MSA/SOW/change orders).
Key Competencies
Partner-centric mindset with strong relationship-building skills
Operational fluency in GMP manufacturing, quality, and regulatory submissions
Strong execution discipline and attention to detail
Clear, concise, and professional communication under pressure
Collaborative leadership without direct authority
Exemplary organizational skills
Experience in timeline management and risk management
Aptitude for working independently under evolving conditions and with a sense of urgency to meet milestones
Ability to respond quickly and effectively to evolving priorities
Proficiency in active problem-solving and driving issues to resolution
Proven ability to achieve results in a virtual setting