CMC Program Lead - Illuccix and Gozellix

OpenKrill; United States; On-site; USD 150,000 - 190,000; Full time

Benefits offered by this job

Equity-based incentive program

Bonuses and performance incentives

Generous vacation

Wellness days

Learning and development support

Job summary

Telix Pharmaceuticals seeks a CMC Program Lead to ensure readiness of radiopharmaceutical assets for commercial viability and global expansion. You will coordinate CMC activities across API, Fill/Finish, and Secondary Packaging with internal teams and external partners.

You will drive cross-functional programs, manage timelines and budgets, and communicate risks to senior leadership while supporting lifecycle management and regulatory filings.

Qualifications

• BA or BS degree in Business, Science, Mathematics, Engineering, or a related scientific discipline required.
• 8+ years of radiopharmaceutical/pharmaceutical/biopharma CMC experience with (optional) 2+ years of CMC program/project management.
• Experience in working with cross-functional teams, external partners and CDMOs required.
• Excellent communication, collaboration, and change management skills.
• Robust knowledge of FDA and global regulatory requirements; strong technical understanding of manufacturing.
• Must have strong experience in MS Office suite applications and management software (e.g., SAP, MS Project, Smartsheet).
• Ability to thrive in a dynamic, global environment with travel 10-20%.

Responsibilities

• Plan, coordinate, and deliver CMC strategies, plans, and deliverables for radiopharmaceutical drug candidates through filing readiness.
• Represent the CMC team on the global matrix team for assigned projects.
• Lead internal CMC project teams across technical SMEs, Supply Chain, Validation, Quality, and Regulatory.
• Establish and maintain CMC project dashboards, timelines, and budgets.
• Track CMC deliverables, manage PO requests, and incorporate CMC plans into overall project plans.
• Outline CMC risks and mitigation strategies; communicate to management.
• Provide regular CMC updates to senior management on status and KPIs.
• Lead CDMO/CMO CMC vendor selection and manage relationships with manufacturing partners.
• Collaborate with Global Product Development Leads and external partners to maintain integrated plans.

Skills

Cross-functional

Communication

Change management

Initiative

Adaptability

Teamwork

Problem solving

Education

BA/BS in related field

Tools

SAP

MS Project

Smartsheet

Job description

Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation. At our core, we exist to create products that seek to improve the quality of life for people living with cancer and rare diseases. You will be supporting the international roll-out of our approved prostate cancer imaging agent and helping us to advance our portfolio of late clinical-stage products that address significant unmet need in oncology and rare diseases.

See Yourself at Telix

As the CMC Program Lead covering Illuccix and Gozellix, you will play a critical role in ensuring successful readiness of the company’s radiopharmaceutical assets for ongoing commercial viability, market expansion, and process improvement. Ensuring the effective execution of CMC strategies through the cross functional collaboration of internal and external partners. The CMC Program Lead will be responsible for coordinating and delivering CMC activities at API, Fill/Finish, and Secondary Packaging partners in line with project requirements and company goals for assigned CMC development programs. The CMC Program Lead will be the program matrix team representative for CMC and be responsible for driving activities across the CMC disciplines.

Key Accountabilities:

• Plan, coordinate, and deliver CMC strategies, plans, and deliverables for radiopharmaceutical drug candidates including a hand-off at pivotal Phase 3 studies through filing readiness, NDA/MAA/BLA submissions, and ultimately ongoing commercial life-cycle management
• Along with the CMC PL covering radioactive manufacturing, representing the CMC team on the global matrix team for the assigned projects
• Facilitate, manage, and lead internal CMC project teams comprised of technical CMC SMEs, Supply Chain, Logistics, Validation, Quality, Clinical Ops, and Regulatory
• Establish and maintain CMC project dashboards, timelines, and budgets for assigned projects
• Track CMC deliverables, initiate PO requests, drive out of budget requests, approve invoices, and ensure the CMC strategies and plans are incorporated into the overall project plans
• Proactively outline CMC risks and mitigation strategies, and communicate risks and issues to project teams and senior management
• Provide regular CMC updates to senior management on project status, timelines, risks, issues, KPIs, and forecasting for future project needs
• Lead CDMO/CMO CMC vendor selection process in collaboration with Procurement, Quality and CMC SMEs, and serve as the relationship lead to our internal and external contract manufacturing partners
• Partner closely with all key stakeholders of the internal Telix teams, including Global Product Development Leads, Global Brand Leads, and external CDMO/CMOs to develop and maintain integrated project plans to identify/communicate interdependencies as well as critical path activities for the program
• Partner with development CMC Program Leads to plan hand-offs enabling smooth transitions from development to commercial and lifecycle management
• Facilitate team meetings using project management best practices/tools to drive cross-functional communication, timely and effective decision making, and successful execution of project objectives
• Organize and maintain CMC team communications including meeting agendas, minutes, decision logs, task lists, and risk analyses/mitigation strategies
• Identify gaps in processes, then work with appropriate parties to develop and implement solutions.
• Plan program and commercial budget along with Supply Chain, Program Management, and Finance.
• Drive change controls for complex CMC items such as product launch in expanded regions, product labeling changes, process improvement requiring filings, and more.

Position Requirements

Education and Experience:

• BA or BS degree in Business, Science, Mathematics, Engineering, or a related scientific discipline required
• 8+ years of relevant radiopharmaceutical/pharmaceutical/biopharma CMC experience with (optional) 2+ years of CMC program/project management experience.
• Experience in working with cross-functional teams, external partners and CDMOs required
• Excellent communication, collaboration, and change management skills
• Robust knowledge of FDA and global regulatory requirements. Also possesses a strong technical understanding of manufacturing, radiopharmaceuticals, and product/process development
• Must have strong experience in MS Office suite applications and management software (e.g., SAP, MS Project, Smartsheet)
• Strong foundational collaboration skills with experience working in a successful matrix managed environment.
• Ability to demonstrate initiative, suggest improvements to current systems as well as establish new processes
• Able to thrive in a highly dynamic, fast paced, continuously changing global environment with minimal oversight/direction.
• Ability to travel 10-20% to manage collaborations with global team members and CDMOs

Key Capabilities:

• Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do
• Results-oriented: Driven to achieve goals and objectives, with a strong focus on delivering measurable results
• Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges
• Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels, using clear and concise language
• Collaboration: Work effectively as part of a team, actively sharing knowledge and expertise to achieve common goals
• Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges
• Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected
• Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges
• Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders
• Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills

At Telix, we believe everyone counts, we strive to be extraordinary, and we pursue our goals with determination and integrity. You will be part of an engaged and supportive group of colleagues who all have a shared purpose: to help people with cancer and rare diseases live longer, better quality lives. Being a Telix employee means being a part of a unique, global, interdisciplinary team working to deliver what's next in precision medicine. We have hybrid and remote employees located all around the world. We offer competitive salaries, annual performance-based bonuses, an equity-based incentive program, generous vacation, paid wellness days and support for learning and development.

Telix Pharmaceuticals is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.

VIEW OUR PRIVACY POLICY HERE