Director, Manufacturing Operations

🔥 0 minutes ago

🇨🇦 Canada – Remote

⏰ Full Time

🔴 Lead

⚙️ Operations

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Telix Pharmaceuticals Limited

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 2015

🏥 Healthcare

💼 Consulting

🧬 Biotechnology

Healthcare • Consulting • Biotechnology

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

• Develop manufacturing and operational plans for commercial and late-stage clinical assets • Collaborate with Regional Operations leadership, Supply Chain, Program leadership, and Directors of CMC Programs • Ensure effective leadership, execution, and delivery of process development and improvement • Ensure contract and regulatory compliance and commercial viability • Plan global production, supply chain, logistics, and distribution • Oversee subject matter experts in Small Molecule API, Aseptic Fill/Finish, and Secondary Packaging • Partner with contract manufacturers to ensure quality, deliveries, and costs meet or exceed expectations • Oversee manufacturing, quality, and product development from mid-stage clinical through commercial launch • Develop CDMO strategies for cost savings, supply redundancy, and process improvement • Manage complex technical issues and support quality investigations and non-conformances • Lead and manage manufacturing engineers, including coaching and performance management • Serve as technical lead for supplier and contracting-organization business reviews • Oversee technical transfers and process validation at internal and external CDMOs

🎯 Requirements

• BA or BS degree in Engineering, Biology, Chemistry, or other relevant field • 10+ years combined experience in late-stage clinical to commercial cGMP Manufacturing, Engineering, Contract Manufacturing, and/or Quality • 3+ years of previous management experience • Direct experience in Sterile Injectable Filling and Lyophilization of Drug Product/Substances supporting both clinical and commercial products • Direct experience in Secondary Packaging of Parenteral drugs preferred • Direct experience in complex formulations of bulk drug substances and biologic drug substance manufacturing preferred • Experience working with International Contract Manufacturing Organizations • Ability to travel approximately 30%—both domestically and internationally • Strong communication, collaboration, adaptability, and ethical behavior • Commitment to continuous learning and professional development

🏖️ Benefits

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