Associate Director, Discovery Radiochemistry

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Associate Director, Discovery Radiochemistry

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locations

CA: Toronto Point

time type

Full time

posted on

Posted Yesterday

job requisition id

R-63531

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.
About POINT Biopharma:
POINT Biopharma Global Inc. is a globally focused radiopharmaceutical company building a platform for the clinical development and commercialization of radioligands that fight cancer. Recently acquired by Eli Lilly and Company, POINT aims to transform precision oncology by combining a portfolio of targeted radioligand assets, a seasoned management team, an industry-leading pipeline, in-house manufacturing capabilities, and secured supply for medical isotopes including actinium-225 and lutetium-177. POINT is a wholly owned subsidiary of Eli Lilly and Company.
Position Summary:
The Associate Director of Discovery Radiochemistry will be a leader and scientific expert in the discovery and development of novel radioligands for use in cancer imaging and therapy. They will work in collaboration with team members, other departments, and external partners (CDMOs) to lead the development of novel radioligands, enable the supply of radiolabeled compounds for preclinical experiments, conduct formulation development, and support the development of radiopharmaceutical manufacturing processes for clinical development.
Roles and Responsibilities of the Position:
Demonstrate leadership and management capabilities
Oversee the development of the next-generation of radiopharmaceuticals by leading radiochemistry research and development for discovery programs
Produce and supply radiolabeled compounds to support the preclinical evaluation of novel radioligands
Design and conduct radiolabelling and formulation optimization studies
Evaluate and integrate novel technology into the Discovery Radiochemistry team’s workflow
Support the development of cGMP radiopharmaceutical manufacturing processes to enable clinical development activities
Collaborate and communicate effectively with a multidisciplinary team including Preclinical, Translational Radiochemistry, Quality Assurance, and Facilities
Interact and maintain strong collaborative relationships with stakeholders including business and industry partners
Proactively tracking of innovation and supporting IP filing activities
Prepare and deliver presentation for internal and external team meetings
Author development reports, manuscripts for publication in journals, and patent applications
Required Qualifications:
PhD in radiochemistry, organic chemistry, chemical engineering, or a related discipline.
Minimum of 7 years of industry experience in the development of novel radiopharmaceuticals
Minimum of 3 years of supervisory or management experience in radiochemistry development or radiopharmaceutical manufacturing.
Demonstrated project management experience
Experienced in radiochemistry development including imaging radioisotopes (ie. F-18, Ga-68, Cu-64, Zr-89, In-111) and therapeutic radioisotopes (ie. Lu-177, Ac-225, Tb-161, Cu-67, Pb-212).
Experienced in quality control testing of radiopharmaceuticals including radio-HPLC, radio-ITLC and GC.
Functional understanding of the principles of cGMP radiochemistry production requirements
Proven ability to work independently with strong organization and communication skills.
Demonstrated ability to successfully prioritize projects and manage timelines in a fast-paced environment.
Functional knowledge of GMPs and applicable FDA, EMA, Health Canada, USP, ICH and PDA guidelines.
Additional Preferences :
Knowledge of environmental health and radioprotection requirements are considered assets.
Physical Demands/Travel:
Position will require 0 to 20% of travel within North America and abroad into the EU. A valid passport and eligible to travel into these countries are required.
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Work Environment:
Position is required to be onsite downtown Toronto during the work week.
This role works in a hospital setting and it is mandatory for all employees to complete health screens before onboarding. In the event the screen results show non-immunity, vaccines may need to be administered.
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Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Eli Lilly Canada is committed to employment equity. We encourage applications from qualified women, members of visible minorities, aboriginal peoples, and persons with disabilities.
Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources (

[email protected]

) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response.
Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources (

[email protected]

) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response.
Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
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About Us

At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world.How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people.We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe!

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