Sr Manager, Facilities and Supply Chain

See Yourself at Telix

The Sr Manager, Facilities and Supply Chain will lead and implement a culture of continuous improvement across the facilities and supply chain department within a radiopharmaceutical manufacturing environment. This role will work closely with the Operations and Quality teams in establishing the long-term facility operations strategy for the ITG site. This role will work with Telix Global Supply Chain to support supply chain and logistics standards for products coming to or leaving ITG. The role is on-site, located in Angleton Texas. 

Key Accountabilities:

• Drive the Operational Excellence strategy aligned with corporate goals.
• Support the development and implementation of goals and objectives and associated budgets for all facility services and maintenance programs.
• Ensure that procedures are in place for cGMP and daily activities and are followed by area personnel and contractors.
• Ensures consistent management and maintenance practices throughout the facilities and sites with regards to services provided.
• Provide support as required, including outside of normal working hours to maintain continuous and compliant (safety, quality, etc.) facility operations at the site.
• Provide expertise and resources for analytical and manufacturing equipment installation and qualification. Experience with typical radiopharmaceutical equipment (radio TLC, Dose calibrators, gamma counters, etc is a plus) 
• Build/maintain a team to support the outbound logistics of radioactive drug product and/or device transportation logistics. 
• Coordinate international logistics with the Telix logistics team
• Maintain and manage the metrology department for all GMP equipment.  
• Coordinate maintenance for GMP equipment using internal or external qualified suppliers.  
• Personal development – maintain standard knowledge and make recommendations for professional development and training. 

Position Requirements

Education and Experience: 

• Bachelor’s degree with orientation in pharmacy, biochemistry or science field or equivalent expereince in GMP manufacturing 
• Minimum 8 years’ of experience in pharmaceutical or biotechnology manufacturing environment with Good Manufacturing Practices (GMP) +3 years of leadership experience
• Experience working in close support with R&D, Operations and Quality.
• Experience working in radiopharmaceuticals or radionuclide(s) manufacturing (highly preferred),
• Strong written and oral communication skills required.
• Technical understanding of manufacturing, quality and regulatory requirements. 

Key Capabilities:

• Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do
• Results-oriented: Driven to achieve goals and objectives, with a strong focus on delivering measurable results
• Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges
• Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels, using clear and concise language
• Collaboration: Work effectively as part of a team, actively sharing knowledge and expertise to achieve common goals
• Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges
• Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected
• Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges
• Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders
• Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills