Global Manufacturing Engineer

🕒 May 22

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Telix Pharmaceuticals Limited

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 2015

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Biotechnology • Pharmaceuticals • Healthcare Insurance

Telix Pharmaceuticals Limited is a commercial-stage biopharmaceutical company dedicated to transforming the way cancer and rare diseases are diagnosed and treated. Focusing on the development and commercialization of theranostic radiopharmaceuticals, Telix utilizes targeted radiation to enhance treatment decision-making and deliver personalized therapy. With an extensive pipeline addressing areas such as prostate and kidney cancer, neuro-oncology, and musculoskeletal cancers, Telix has garnered global regulatory approvals for its lead imaging agent, Illuccix®, and is actively conducting numerous clinical trials worldwide.

📋 Description

• Provide technical expertise for process development and manufacturing activities related to bulk formulation, fill/finish, lyophilization, and packaging of small molecules and biologics • Analyze production processes and report results, identifying and communicating gaps, risks, and inefficiencies • Drive implementation of process improvements and risk mitigations • Lead manufacturing investigations and root cause analysis • Manage technical collaborations with multiple contract development/manufacturing organizations (CDMOs) • Author and review external manufacturing operation documents such as SOPs, batch records, protocols, and reports • Ensure appropriate compliance through document creation/review/approval, quality investigations, corrective actions, and change control within a Quality system

🎯 Requirements

• Science or engineering degree with 4+ years of relevant operational pharmaceutical experience across a breadth of functions including but not limited to, manufacturing operations, bioprocessing technology, validation, and engineering • Experience in MS Office suite applications (e.g., Excel, Word, Project) • Experience working with cross-functional teams, external partners and CDMOs • Experience in authoring challenging technical documents, including but not limited to, protocols, reports, CMC modules, and filing response • Strong experience in a key functional area within pharmaceutical operations • Experience in pharmaceutical and process development

🏖️ Benefits

• Competitive salaries • Annual performance-based bonuses • Equity-based incentive program • Generous vacation • Paid wellness days • Support for learning and development