Associate Director, CMC, Program Management
Amylyx Pharmaceuticals
Summary
Amylyx is seeking an experienced Associate Director, CMC Program Management to provide strategic and operational program management leadership across our CMC portfolio. This individual will partner closely with CMC asset leads and colleagues across Regulatory, Quality, Analytical Development, Supply Chain, External Manufacturing, Clinical, and Nonclinical Development to translate CMC strategies into integrated, executable plans.
Job description
The Opportunity
Amylyx is seeking an experienced Associate Director, CMC Program Management to provide strategic and operational program management leadership across our CMC portfolio. This individual will partner closely with CMC asset leads and colleagues across Regulatory, Quality, Analytical Development, Supply Chain, External Manufacturing, Clinical, and Nonclinical Development to translate CMC strategies into integrated, executable plans.
The Associate Director will establish clear timelines, milestones, dependencies, budgets, and governance practices for assigned CMC programs. This role will facilitate CMC teams, monitor critical-path activities, drive timely decision-making, identify and escalate risks, and ensure that technical, manufacturing, and regulatory deliverables remain aligned with program objectives.
Responsibilities
- Lead program management for one or more CMC programs, developing and maintaining integrated plans that include scope, timelines, milestones, dependencies, deliverables, resources, budgets, and key decision points.
- Partner with CMC asset leads and functional subject matter experts to translate CMC strategy into coordinated execution plans that support development, manufacturing, lifecycle management, regulatory filings, and program objectives.
- Lead CMC team meetings and governance processes, including agendas, minutes, action-item tracking, decision logs, risk registers, and escalation of issues requiring leadership attention.
- Proactively monitor critical-path activities, identify strategic and operational risks, assess downstream impacts, and partner with stakeholders to develop mitigation and contingency plans.
- Coordinate CMC deliverables across Regulatory, Quality, Analytical Development, Technical Development, and Supply Chain ensuring clear ownership, accountability, and communication across workstreams.
- Develop concise program dashboards and status reports that provide visibility into milestones, risks, decisions, budget status, resource needs, and overall CMC readiness.
- Support planning and execution of complex CMC initiatives, which may include technical transfers, process development and validation activities, regulatory submission readiness, and lifecycle-management programs.
- Establish and continuously improve scalable CMC program management tools, templates, metrics, meeting structures, and ways of working that strengthen execution across the broader CMC organization.
Required Qualifications
- Bachelor's degree in life sciences, chemistry, engineering, pharmaceutical sciences, or a related discipline.
- Eight to ten years of relevant experience in the pharmaceutical or biotechnology industry, including significant experience in project or program management supporting CMC, Technical Operations, manufacturing, or product development.
- Demonstrated understanding of CMC development, regulatory CMC requirements, and cGMP-compliant pharmaceutical development and manufacturing.
- Experience building and managing complex, integrated plans across multiple technical workstreams, including timelines, milestones, dependencies, risks, budgets, and resource requirements.
- Proven ability to lead cross-functional teams and drive execution through influence in a matrixed environment without relying on direct authority.
- Experience proactively identifying, communicating, escalating, and managing program risks, issues, decisions, and competing priorities.
- Strong written, verbal, facilitation, stakeholder-management, analytical, and organizational skills, with the ability to communicate technical and program information clearly to different audiences.
- Proficiency with project-management and collaboration tools used to maintain plans, trackers, dashboards, actions, and program documentation.
Preferred Requirements
- Master's degree in a scientific, engineering, or business discipline.
- Direct experience supporting CMC programs from early development through late-stage development, and commercialization readiness.
- Project Management Professional certification or an equivalent project or program management credential, along with experience using tools such as Smartsheet, Microsoft Project, or SharePoint.
Requirements
- Bachelor's degree in life sciences, chemistry, engineering, pharmaceutical sciences, or a related discipline
- Eight to ten years of relevant experience in the pharmaceutical or biotechnology industry
- Significant experience in project or program management supporting CMC, Technical Operations, manufacturing, or product development
- Demonstrated understanding of CMC development, regulatory CMC requirements, and cGMP-compliant pharmaceutical development and manufacturing
- Experience building and managing complex, integrated plans across multiple technical workstreams
- Proven ability to lead cross-functional teams and drive execution through influence in a matrixed environment
- Experience proactively identifying, communicating, escalating, and managing program risks, issues, decisions, and competing priorities
- Strong written, verbal, facilitation, stakeholder-management, analytical, and organizational skills
- Proficiency with project-management and collaboration tools
- Master's degree in a scientific, engineering, or business discipline (preferred)
- Direct experience supporting CMC programs from early development through late-stage development and commercialization readiness (preferred)
- Project Management Professional certification or equivalent credential (preferred)
- Experience using Smartsheet, Microsoft Project, or SharePoint (preferred)
Benefits
- Health Insurance
- Performance-based bonuses
- Equity awards
- Comprehensive benefits package
Company overview
Amylyx Pharmaceuticals is a clinical-stage pharmaceutical company based in Cambridge, Massachusetts, founded in 2013 by co-CEOs Josh Cohen and Justin Klee. The company specializes in developing novel therapies for neurodegenerative diseases with high unmet medical needs, with a particular focus on amyotrophic lateral sclerosis (ALS), Wolfram syndrome, and post-bariatric hypoglycemia. Amylyx's lead investigational therapy, AMX0035, received FDA approval for ALS treatment under the brand name RELYVRIO in September 2022. The company employs a rigorous scientific approach to target multiple pathological pathways in neurodegeneration, with additional pipeline candidates including avexitide for metabolic disorders and AMX0114, an antisense oligonucleotide targeting calpain-2 for ALS. With a team of 201-500 employees, Amylyx combines therapeutic development expertise with commercialization capabilities to address some of medicine's most challenging conditions.