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Radiopharmaceuticals Jobs (NOW HIRING)

Reviews and releases batches of PET radiopharmaceuticals manufactured under 21 CFR 212, cGMP PET drug manufacturing regulations. 4.Ensures compliance with all state, federal, and local regulations ...

Reviews and releases batches of PET radiopharmaceuticals manufactured under 21 CFR 212, cGMP PET drug manufacturing regulations. 4.Ensures compliance with all state, federal, and local regulations ...

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How much do radiopharmaceuticals jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for radiopharmaceuticals in the United States is $51.91, according to ZipRecruiter salary data. Most workers in this role earn between $39.18 and $62.50 per hour, depending on experience, location, and employer.

What is a radiopharmaceutical?

A job in radiopharmaceuticals involves the research, development, production, and safe handling of radioactive drugs used in medical imaging and treatment. Professionals in this field work in laboratories, hospitals, or pharmaceutical companies to ensure compliance with safety regulations and quality standards. Roles may include radiochemists, pharmacists, or nuclear medicine technologists who prepare and administer these compounds for patient diagnosis and therapy. This career requires a strong background in chemistry, biology, and radiation safety.

What skills and qualifications are needed to thrive as a radiopharmaceutical specialist?

Excelling in Radiopharmaceuticals requires a solid background in chemistry, pharmacology, and radiation safety, often supported by a relevant science degree and specialized training or certification in nuclear medicine. Familiarity with radiopharmacy equipment, quality control systems, and regulatory compliance software is critical. Strong attention to detail, problem-solving skills, and effective communication enhance performance in multidisciplinary healthcare environments. These capabilities ensure the safe preparation, handling, and administration of radiopharmaceuticals, safeguarding both patient health and compliance with strict industry regulations.

What types of teams or professionals do radiopharmaceutical specialists typically collaborate with in their daily work?

Radiopharmaceutical specialists routinely work alongside nuclear medicine technologists, physicians, pharmacists, and laboratory personnel to ensure the safe and effective use of radioactive compounds in diagnostic and therapeutic procedures. Collaboration is essential for accurate dosing, adherence to safety protocols, and timely delivery of radiopharmaceutical products to patients or departments. This teamwork often extends to compliance officers and regulatory agencies as well, given the strict oversight in this field. Working in such an interdisciplinary environment fosters continuous learning and supports the delivery of high-quality patient care.

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What cities are hiring for Radiopharmaceuticals jobs?

Cities with the most Radiopharmaceuticals job openings:

What are the most commonly searched types of Radiopharmaceuticals jobs?

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Infographic showing various Radiopharmaceuticals job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $107,964 per year, or $51.9 per hour.

Scientist, Analytical Method Development - Radiopharmaceuticals

SK Life Science, Inc.

Paramus, NJ

$120K - $140K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted yesterday

New


Job description

The Scientist, Analytical Method Development for Radiopharmaceuticals, is responsible for the development, optimization, validation, and transfer of analytical methods supporting radiopharmaceutical products across early- and late-stage development. This role requires strong technical expertise in analytical chemistry and a solid understanding of the unique challenges associated with radiopharmaceuticals, including short half-life materials, radioactive impurities, and time-critical testing. The position sits within CMC organization and works closely with Quality, Manufacturing, and external partners to ensure robust, compliant, and transferable analytical methods.


Analytical Method Development

  • Working with CDMOs, develop, optimize, and qualify analytical methods to support radiopharmaceutical drug substance and drug product development
  • Design methods suitable for radioactive materials, accounting for decay, sensitivity, speed, and radiation safety considerations
  • Apply a range of analytical techniques, including but not limited to HPLC/UPLC, radio-HPLC, GC, TLC, radio-TLC, spectroscopy, and wet chemistry methods

Method Validation & Transfer

  • Author and execute method qualification, validation, and verification protocols in accordance with ICH and regulatory expectations
  • Lead or support analytical method transfer to internal QC laboratories, CDMOs, and external testing sites
  • Troubleshoot method performance issues during transfer and routine testing, ensuring method robustness and reproducibility

Radiopharmaceutical-Specific Testing

  • Support testing of precursors and radiolabeled finished drug products, including identity, purity, potency, and impurity profiling
  • Collaborate with Radiation Safety Officers (RSO) to ensure compliant handling and testing of radioactive materials
  • Develop rapid and fit-for-purpose methods suitable for short half-life products and just-in-time manufacturing models

Documentation & Regulatory Support

  • Prepare and review technical reports, method SOPs, validation reports, and specifications
  • Contribute to CMC sections of regulatory submissions (IND, CTA, IMPD, NDA/BLA) related to analytical methods
  • Support regulatory interactions, audits, and inspections by providing analytical expertise and documentation

Cross-Functional Collaboration & Continuous Improvement

  • Partner with CMC, Process Development, Manufacturing, Quality, and Clinical teams to align analytical strategies with development timelines
  • Support investigation of OOS/OOT results and implement corrective actions as needed
  • Drive continuous improvement initiatives in analytical efficiency, data integrity, and method lifecycle management

Required

  • Bachelor’s degree in Chemistry, Biology, Life Sciences, or a related discipline
  • Minimum of 7 years of experience in the pharmaceutical or biotechnology industry
  • 2–3 years of direct experience working with radiopharmaceutical products
  • Strong hands-on experience in analytical method development and characterization
  • Demonstrated experience with analytical method transfer to internal or external laboratories

Preferred

  • Advanced degree (Master’s or Ph.D.) in Chemistry, Pharmaceutical Sciences, or a related field
  • Experience supporting regulatory submissions involving radiopharmaceuticals
  • Familiarity with GMP environments and data integrity requirements (e.g., ALCOA+)

Key Competencies

  • Strong analytical and problem-solving skills with attention to detail
  • Ability to work effectively in fast-paced, time-sensitive environments
  • Excellent technical writing and documentation skills
  • Strong collaboration and communication skills across cross-functional teams
  • Commitment to quality, compliance, and scientific rigor

Compensation & Benefits

The anticipated salary range for this position is $120,000 to $140,000. Actual compensation may vary based on factors including experience, qualifications, skills, and business needs.

In addition to base salary, SK Life Science offers a competitive benefits package, including a 401(k) plan with company match and medical, dental, and vision coverage. Benefits are subject to eligibility requirements and may be modified at the Company's discretion.