Associate Director, Radiopharmaceutical Development

Role Overview

• Lead radiolabeling, formulation, and analytical method development of small molecules and peptides with different chelators and radiometals.
• Organize, manage, and execute technology transfer to CDMOs.
• Oversee the technical development of ARTBIO’s products with CDMOs.
• Direct the internal ARTBIO team and CDMO teams in generating comprehensive CMC data packages in compliance with regulatory requirements, ensuring a seamless regulatory submission.
• Monitor the production and analytical data of CDMOs to ensure the process is robust and in control.
• Enhance internal technical and operational capabilities to develop the platform, including ongoing monitoring, enhancement, and troubleshooting, and future product development.
• Select and qualify suitable raw materials and ingredients that conform to regulatory requirements.
• Collaborate with senior leaders to develop project plans, timelines, budgets, and teams in alignment with the company’s goals.
• Collaborate with internal and external stakeholders, including research and development, pre-clinical and clinical, quality control, quality assurance, and regulatory teams to drive project success.
• Identify and implement methods and cutting-edge technologies to enhance processes and improve operational efficiencies in radiopharmaceutical development. Offer direction to the top management team on how ARTBIO can competitively leverage these developments.
• Build the KPI scorecards to monitor CDMO performance and troubleshooting.
• Development formulation from preclinical to clinical phase in accordance with FDA and EMEA guidance.
• Establish procedures for good manufacturing practices, safety, reliability, and a commitment to excellence.
• Develop and maintain relationships with key suppliers and service providers to ensure the reliable and efficient supply of raw materials, equipment, and services.
• Ensure compliance with all relevant regulations, standards, and guidelines, including those relating to quality, safety, and environmental impact for our CDMOs, internal R&D, and own projects.

Requirements

• PhD in Radiochemistry, Chemical Engineering, Radiopharmaceuticals, or related fields within life sciences.
• Minimum of 5 years of experience in the radiopharmaceutical field, with a focus on manufacturing and process development.
• Experience and familiarity with GMP environments and radiopharmaceutical manufacturing processes.
• Demonstrated experience in developing and operating complex technologies, ideally in the field of radio ligand therapy (RLT).
• Experience managing a team of technical persons and scientists, with a track record of delivering projects on time, within budget, and to the required safety and quality standards.
• Strong technical knowledge and problem-solving skills in formulation, radiolysis, process validation, qualification of synthesis module, RadioTLC, RadioHPC, Germanium detector, and radiopharmaceuticals, with the ability to think strategically and communicate effectively with cross-functional colleagues.
• Excellent organizational and project management skills, with the ability to prioritize and multitask effectively.
• Familiarity with relevant regulations (FDA, EMA), standards, and guidelines, including those relating to quality, safety, and environmental impact.
• Excellent know-how on regulatory requirements related to drug development.
• Exceptional interpersonal and communication skills with a proven ability to lead teams, foster collaboration, and build strong working relationships.
• Capacity to work autonomously, manage multiple priorities, and deliver high-quality results within tight deadlines.
• Highly organized with commitment to precision, quality, and compliance in all aspects of work.
• Willingness to work extended hours as needed to meet project demands
• Passion to explore novel new technologies related to RLT development.
• Willingness to travel within the country and outside the country.
• Written and verbal fluency in English.

Benefits

• EEO Statement: ARTBIO is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. If you have a disability or special need that requires accommodation, please let us know.
• Questions and Application Process: If interested, please apply and send your CV to HR@artbio.com. All inquiries are treated confidentially.
• ARTBIO does not accept unsolicited resumes from external agencies or recruiters. Submission of a resume without a prior written agreement does not create any express or implied contract between ARTBIO and the agency. ARTBIO will not pay any fees related to unsolicited resumes.