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Radiopharmaceutical Development Jobs (NOW HIRING)

Orano

Process Development Scientist

Plano, TX · On-site

We are seeking a highly motivated Process Development Scientist with expertise in radiopharmaceutical development to join our CMC team. The successful candidate will design, execute, and analyze ...

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How much do radiopharmaceutical development jobs pay per year?

As of Jul 27, 2026, the average yearly pay for radiopharmaceutical development in the United States is $70,347.00, according to ZipRecruiter salary data. Most workers in this role earn between $49,000.00 and $90,000.00 per year, depending on experience, location, and employer.

What are some common challenges faced when working in radiopharmaceutical development, and how can they be managed?

Professionals in radiopharmaceutical development often encounter challenges such as strict regulatory requirements, handling short-lived radioactive materials, and ensuring product sterility. Managing these challenges requires meticulous attention to detail, adherence to safety protocols, and effective collaboration with multidisciplinary teams, including chemists, pharmacists, and regulatory specialists. Regular training, clear communication, and staying updated with industry standards are essential for maintaining a safe and productive work environment.

What is the difference between Radiopharmaceutical Development vs Radiopharmacist?

AspectRadiopharmaceutical DevelopmentRadiopharmacist
CredentialsAdvanced degrees in radiochemistry, pharmaceutical sciences, or related fieldsLicensed pharmacist with specialized training in radiopharmacy
Work EnvironmentResearch labs, pharmaceutical companies, clinical trial settingsHospitals, nuclear pharmacies, clinical settings
Industry UsageDrug development, formulation, and testing of new radiopharmaceuticalsPreparation, dispensing, and safety management of radiopharmaceuticals for patient use

Radiopharmaceutical Development focuses on creating and testing new radiopharmaceuticals in research and industry settings, while Radiopharmacists specialize in preparing and dispensing these drugs in clinical environments. Both roles require specialized knowledge but serve different stages of the radiopharmaceutical lifecycle.

What are the key skills and qualifications needed to thrive in Radiopharmaceutical Development, and why are they important?

To excel in Radiopharmaceutical Development, you need a solid background in chemistry, pharmacology, and radiochemistry, typically supported by an advanced degree in a related scientific field. Familiarity with laboratory instrumentation, Good Manufacturing Practices (GMP), and regulatory compliance systems is essential. Strong problem-solving skills, attention to detail, and effective teamwork set top professionals apart. These competencies are crucial for ensuring the safe, effective, and compliant creation of radiopharmaceuticals for medical imaging and therapy.

What is radiopharmaceutical development?

Radiopharmaceutical development is the process of designing, synthesizing, and testing radioactive compounds used for diagnosis or treatment in nuclear medicine. These compounds, called radiopharmaceuticals, are carefully engineered to target specific tissues or diseases within the body, such as cancer or neurological disorders. The development process involves multidisciplinary teams working in chemistry, biology, and medical imaging to ensure the safety and effectiveness of these drugs before they reach clinical use.
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What cities are hiring for Radiopharmaceutical Development jobs? Cities with the most Radiopharmaceutical Development job openings:
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Radiopharmaceutical Development jobs near you
Infographic showing various Radiopharmaceutical Development job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 82% Full Time, 15% Part Time, and 2% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $70,347 per year, or $33.8 per hour.

Associate Director, Radiopharmaceutical Development

ARTBIO

Cambridge, MA • On-site

Full-time

Posted 7 hours ago

Job description

Summary
As part of ARTBIO’s CMC team, the Associate Director will drive the radiopharmaceutical development of Radioligand Therapy (RLT) products by designing radiolabeling synthesis, formulation, and process development. This role will collaborate with a multidisciplinary team of CDMOs (Contract Drug Manufacturing Organizations) to troubleshoot the manufacturing process of our lead products, ensuring timely data packages for regulatory submissions in compliance with regulatory standards and aligned with corporate objectives. The candidate will also be responsible for setting up the technical transfers necessary to support clinical trials.
 
The ideal candidate is an expert thinker with attention to detail in manufacturing data analysis, high technical proficiency in radiopharmaceutical development, and demonstrated experience with radio metal chemistry, formulation development, and analytical expertise.
Responsibilities
  • 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.
Qualifications & Experience
  • 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.
About Us
Channeling Energy. Changing Lives. ARTBIO redefines cancer care by discovering and developing a new class of Alpha Radioligand Therapies (ARTs), powered by unique Pb-212 isotope technology and seamless supply. Our team works tirelessly to bring therapies that matter to patients who need them.
 
The unique ARTBIO approach selects the optimal alpha-precursor isotope (212Pb) and tumor-specific targets to create therapeutics with the potential for the highest efficacy and safety. The company's AlphaDirect™ technology, a first-of-its-kind 212Pb isolation method, enables a distributed manufacturing approach for the reliable production and delivery of ARTs. ARTBIO is advancing multiple pipeline programs, with lead program AB001 currently in first-in-human trials. The company is shaped by a long-standing scientific legacy with nearly a century of pioneering work in radiation therapy conducted at the University of Oslo and Norway’s Radium Hospital.
 
Cancer is relentless. So are we. We are driven by a desire to do better for cancer patients, lowering the burden of toleration and safety while at the same time raising the bar on clinical efficacy and duration. As an emerging, global biotech with locations in Boston, Basel, London, and Oslo, we take advantage of diverse scientific depth and insights, which makes ARTBIO a unique place to work. 

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.