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Scientist I, Chemistry Installation

Telix Pharmaceuticals (AMER)

Location
British Columbia - Burnaby · Canada
Department
Education
Experience
1+ years

Description

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 Scientist I, Chemistry Installation Training & Development is responsible for supporting the Company's chemistry installation training programs and chemistry product development initiatives. This role ensures that customer technical support activities, and Quality Assurance (QA) requirements are met through effective collaboration with internal and external stakeholders.

The position requires expertise in radiochemistry, radioisotope production, and nuclear physics to support chemistry installation, process optimization, troubleshooting, and product development activities. The successful candidate will contribute to the design, implementation, and continuous improvement of chemistry training programs and product development processes while ensuring compliance with GMP and ISO 9001 standards, applicable regulatory requirements, and customer expectations.

Key Accountabilities:

  • Support chemistry installation training activities for customers, ensuring successful implementation, knowledge transfer, and compliance with established procedures and quality standards.
  • Participate in discussions regarding the implementation of new products and technologies, maintaining regular communication with customers to understand and define technical and operational requirements.
  • Serve as an internal technical resource for radiochemistry, radioisotope production, and nuclear-related inquiries, including the interpretation of nuclear data and evaluation of production parameters.
  • Apply theoretical and practical knowledge of nuclear physics and radiochemistry to troubleshoot and optimize production workflows, including isotope yield calculations, decay analyses, radiation shielding assessments, and activation
  • Support chemistry product development programs through experimental work, process evaluation, data analysis, and validation activities.
  • Contribute to the development, review, implementation, and continuous improvement of standard operating procedures (SOPs), work instructions, and technical documentation related to chemistry installation, radiochemical processing, and product
  • Ensure compliance with internal QA/QC programs, ISO 9001 and GMP requirements, regulatory standards, and radiation safety
  • Assist in root cause investigations, deviation assessments, and risk analyses associated with manufacturing, installation, or product development activities, providing scientific recommendations and corrective actions as required.
  • Collaborate with cross-functional teams, customers, vendors, and external partners to coordinate installation, training, research, and development activities.
  • Support technology transfer, process validation, and continuous improvement initiatives aimed at enhancing product quality, operational efficiency, and customer satisfaction.

Education & Experience 

  • BS or MS in Chemistry, Radiochemistry, Nuclear Engineering, Physics, or a related scientific discipline and 1 year of experience required.
  • Experience with various analytical equipment for radioisotope quality control such as chromatography instruments, radiation detectors and spectrometers
  • Experience performing of quality control testing in accordance to standard operating
  • Experience in radioisotope production using
  • Demonstrated knowledge of cyclotron systems and
  • Strong technical understanding of radioisotope production, radiochemical separation, purification processes and radioisotope quality control testing.
  • Knowledge of radiation safety principles and handling practices as well as willingness to learn and comply with Canadian Nuclear Safety Commission (CNSC) requirements.
  • Experience supporting technical training, technology transfer, process development, or customer-facing scientific activities is considered an asset.
  • Experience implementing new procedures and executing change orders in accordance to governing quality management systems.
  • Ability to interpret and apply multiple regulatory and quality standards in operational
  • Excellent written and verbal communication
  • Demonstrated commitment to accuracy, data integrity, and quality
  • Demonstrated commitment to safety culture in a laboratory
  • Strong interpersonal skills with the ability to build effective working relationships across multidisciplinary
  • Self-motivated, detail-oriented, and capable of managing multiple priorities while achieving
  • Availability to willingness to travel globally to perform installation and training.

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

 

 

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. 

VIEW OUR PRIVACY POLICY HERE

 

Skills

GMPCompliance

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