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 Site Manager is responsible for overseeing all operations, ensuring the Telix site meets or exceeds all regulatory, quality, and safety standards.
This role requires a deep understanding of radiopharmaceutical production, strict adherence to Good Manufacturing Practices (GMP), and the ability to lead and manage a multidisciplinary team.
This role will require working on-site in our new North Melbourne facility.
Key Accountabilities: Quality Management Uphold the highest standards of product quality by ensuring all processes comply with GMP and other relevant quality standards.
Lead the implementation of quality control procedures and corrective actions where necessary.
Collaborate with the Quality Assurance team to address any quality-related issues promptly.
Safety and Environmental Compliance Promote and enforce a strong safety culture within the site, ensuring all safety protocols and procedures are followed.
Manage radiation safety programs and ensure the site complies with all environmental regulations.
Conduct regular safety audits and implement corrective actions to mitigate risks.
Team Leadership Manage, mentor, and develop a diverse team of professionals, including production, quality, safety, and administrative staff.
Oversee recruitment, training, and performance management to build a high-performing team.
Stakeholder Management Act as the primary point of contact for internal and external stakeholders, including regulatory bodies, suppliers, and customers.
Maintain strong relationships with key stakeholders to support the strategic objectives of the site and the broader organization.
Represent the site in cross-functional meetings and contribute to the overall strategic direction of the business.
Financial Management Oversee the site's budget, ensuring cost-effective operations while maintaining high-quality standards.
Monitor financial performance, identifying areas for cost savings and efficiency improvements.
Prepare and present financial and operational reports to senior management Education and Experience: Bachelor's degree in Chemistry, Engineering, Life Sciences, or a related field.
Advanced degree preferred.
Minimum of 5 years of experience in a pharmaceutical or radiopharmaceutical manufacturing environment, with at least 2 years in a leadership role.
In-depth knowledge of GMP, FDA, and other regulatory requirements for radiopharmaceuticals.
Proven experience in managing complex operations, including production, quality, and safety.
Strong leadership and team management skills with a track record of developing high-performing teams.
Excellent communication and stakeholder management skills.
Ability to make strategic decisions and lead in a fast-paced, regulated environment.
Preferred Skills & Certifications: Certification in Radiation Safety or Nuclear Pharmacy Experience with Lean Manufacturing, Six Sigma, or Kaizen methodologies.
Familiarity with automated radiopharmaceutical production systems and software.
Key Capabilities: Strong communication skills, effective across all levels of the organization.
Extensive experience in Regulatory Affairs, particularly with the TGA in Australia, and ideally, experience working with regulatory authorities across the Asia-Pacific region.
Proficient understanding of both early and late-stage drug development processes, including clinical and non-clinical requirements, at an advanced level.
Strong ability to collaborate effectively with teams across the region.
Demonstrate a dedication to continuous learning and professional growth, actively pursuing opportunities to enhance your expertise and skill set.
Uphold integrity and exhibit a steadfast commitment to ethical conduct in all dealings with colleagues and stakeholders.
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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