Analytical Development Scientific Lead (Radiopharma)
: Job Details :


Analytical Development Scientific Lead (Radiopharma)

EPM Scientific - Phaidon International

Location: Boston,MA, USA

Date: 2024-09-19T06:53:09Z

Job Description:
SUMMARYThis Global Radiopharma is currently looking for an Analytical Development expert to join their R&D leadership team. The ideal candidate will have a strong track record of innovation & prior experience in radiopharmaceutical and nuclear analytical science technology.RESPONSIBILITIES
  • Provide strategic & technical leadership for the Analytical Development team while collaborating with relevant R&D/CMC depts, fostering a culture of innovation, collaboration, and excellence.
  • SME for analytical method development, optimization, qualification & validation to support the advancement of the lead programs in the pipeline
  • Manage CDMOs, setting clear expectations and goals, and conducting performance assessments and oversight of internal and external stakeholders to facilitate efficient technology transfers.
  • Evaluate & implement (when deemed necessary) state-of-the-art technologies and methodologies to enhance analytical capabilities for radiopharma compounds.
  • Ensure accurate and timely documentation of analytical activities, including method development reports, validation protocols, technical reports, & FDA regulatory filing (IND/IMPD/BLA, etc.).QUALIFICATIONS
    • PhD in Analytical Chemistry, Pharmaceutical Sciences, or a related field with 8+ years of experience in the pharmaceutical industry
    • Experience in Radiopharmaceuticals analytical methods (minimum 3 years) in development of radiopharmaceuticals (alpha therapy will be a plus), with a proven track record in analytical method development and technology transfer.
    • Strong leadership and people management skills (Prior experience managing CRO/CMO's is a PLUS).
    • 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. #J-18808-Ljbffr
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