CMC Programs Intern Therapeutics (Tx)

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

The Chemistry, Manufacturing, and Controls (CMC) Intern will play a hands-on role supporting Telix’s CMC team with external manufacturing and CDMO contracting activities. This includes assisting in the preparation and tracking of work orders, reviewing technical statements of work (SOWs), following up on procurement steps, and managing supporting documentation related to contract execution. The intern will also contribute to the development and maintenance of process flow diagrams for complex radiopharmaceutical supply chains.

This internship provides a unique opportunity to gain real-world experience in pharmaceutical operations and cross-functional project coordination. Interns will gain exposure to how new drugs are manufactured, how CDMO partnerships are managed, and how internal systems support regulatory readiness and product delivery. The role is designed to build skills in operational execution, documentation standards, and supply chain process mapping—all within a collaborative and fast-paced biotech environment.

Key Accountabilities

• CDMO Contracting Support: Work alongside CMC leads to prepare and revise technical statements of work (SOWs) and draft work orders that define outsourced manufacturing activities.
• Work Order and Purchase Order Coordination: Support the submission, tracking, and follow-up of approvals for work orders and POs. Communicate with vendors and internal stakeholders to ensure execution stays on schedule.
• Business Process Evaluation: Participate in evaluating and mapping existing operational workflows to identify bottlenecks or inefficiencies in contracting and documentation processes.
• Document Reconciliation: Help maintain accurate version control of contracts and reconcile documentation related to budget line items, executed work, and associated invoices.
• System Uploads and Record Management: Upload finalized contracts and related documents to SharePoint and document control systems. Ensure records are filed correctly and remain accessible to the team.
• Meeting Participation and Notes: Attend internal project and CMC meetings to take structured notes, track follow-up actions, and support meeting documentation using shared tools.
• Tool and Template Development: Assist in refining team templates and tools, such as stage-gate trackers, decision logs, and process flow diagrams, to improve clarity, usability, and operational efficiency.
• Final Internship Presentation: Deliver a short presentation at the end of the internship summarizing your work, lessons learned, and suggestions for improving CMC operational support.
  
  

Education And Experience

• Academic Background
• Currently enrolled in a Bachelor’s or Master’s program in one of the following disciplines:
• Pharmaceutical Sciences
• Chemical Engineering
• Biomedical Engineering
• Biochemistry
• Other life science or technical fields relevant to drug development or operations
• Skills
• Strong organizational skills with close attention to detail
• Proficiency in Microsoft Office tools (Word, Excel, PowerPoint, Teams)
• Ability to follow standard procedures, compliance requirements, and documentation protocols
• Willingness to learn how external manufacturing, vendor engagement, and document control systems function in a regulated environment
• Capable of working independently with minimal supervision after initial onboarding
• Reliable communicator with an interest in learning how cross-functional teams operate in pharmaceutical development
  

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.

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