Telix Pharmaceuticals Limited ir biofarmācijas uzņēmums komercializācijas posmā, kas izstrādā un komercializē teranostiskus radiofarmaceitiskos preparātus vēža un reto slimību ārstēšanai. Uzņēmuma pieeja apvieno mērķētu attēldiagnostiku ar uz starojumu balstītu ārstēšanu, lai atbalstītu informētākus klīniskos lēmumus un personalizētu aprūpi.
Uzņēmuma izstrādes programma aptver prostatas un nieru vēzi, neiroonkoloģiju, kā arī balsta un kustību aparāta vēzi. Telix ir saņēmis globālu regulatīvo iestāžu apstiprinājumu savam vadošajam attēldiagnostikas produktam Illuccix® un turpina attīstīt plašu klīnisko pētījumu programmu visā pasaulē. Tā komanda darbojas veselības aprūpes, biotehnoloģiju un saistītajās komerciālajās jomās, lai radiofarmaceitiskās inovācijas no izstrādes posma nonāktu klīniskajā praksē.
Legal Counsel, Manufacturing and Supply Chain
Provide legal support for Telix’s radiopharmaceutical contract manufacturing business. Draft and negotiate manufacturing, quality, supply, and operational agreements.
Apraksts
- Provide day-to-day legal counsel to Telix Manufacturing Solutions, Telix’s contract manufacturing and radiopharmaceutical production unit.
- Draft, review, and negotiate manufacturing services and master service agreements, quality agreements, supply contracts, statements of work, and change orders.
- Flag compliance issues involving cGMP, radiopharmaceutical imports and exports, manufacturing regulations, and facilities.
- Manage contract disputes, warranty claims, quality matters, and service-level remediation.
- Create and update contract templates, clause libraries, playbooks, and fallback positions.
- Work with Operations, Quality, Procurement, Finance, and Commercial teams.
- Use and improve intake workflows, escalation paths, and contracting tools.
- Track pharmaceutical manufacturing regulations, industry practices, quality law, and supply-chain law.
- Support procurement and agreements covering ARTMS commercial activity, isotope supply, supply chains, logistics, distribution, and operational services.
Prasības
- Juris Doctor, Bachelor of Laws, or equivalent legal qualification.
- Admitted or eligible to practice in the relevant jurisdiction.
- At least six years of experience in commercial, manufacturing, supply-chain, or transactional law.
- Strong contract drafting and negotiation skills.
- Experience managing a high volume of commercial contracts.
- Experience with manufacturing services agreements, supply-chain contracts, quality agreements, or services contracting.
- Familiarity with current Good Manufacturing Practice (cGMP), FDA or TGA manufacturing compliance, or pharmaceutical quality frameworks is a plus.
- In-house experience is preferred but not required; relevant life sciences law firm experience is also considered.
- Sound commercial judgment and careful attention to detail.
- Clear communication with operations leaders, quality professionals, clients, and legal teams.
- A process-improvement mindset.
- Commitment to quality, safety, ethical conduct, and measurable business results.
- Collaboration, resilience, adaptability, continuous learning, and an inclusive mindset.
Priekšrocības
- Competitive salary.
- Annual performance-based bonuses.
- Equity-based incentive program.
- Generous vacation.
- Paid wellness days.
- Learning and development support.
- Hybrid and remote work arrangements.