Remote PET Radiopharmaceutical Project Scientist

Jubilant Pharma Limited; Kansas; On-site; USD 120,000 - 160,000; Full time

Benefits offered by this job

Remote-based role

Health and dental coverage

Generous vacation

401(k) matching

Job summary

Jubilant Radiopharmacies is seeking a Project Scientist to support technology transfer, validation, and onboarding of new PET products across multiple sites. You will collaborate with Operations, Quality, Project Management, and external partners to ensure compliant implementation of processes.

Ideal candidates have 5+ years in tech transfer within pharma/radiopharma, strong technical writing, and project-management skills, with a focus on regulatory compliance and cross-site collaboration.

Qualifications

• Bachelor's degree in a scientific discipline; advanced degree preferred.
• Minimum 5 years of experience in technology transfer, product development, or manufacturing support in pharma/radiopharmaceuticals.
• Experience in commercial manufacturing within a cGMP environment.
• Knowledge of PET radiopharmaceutical manufacturing and relevant regulations (FDA 21 CFR Part 212/211, Part 11, ICH Q9, USP, GAMP 5, ISPE).
• Experience with validation, qualification, risk assessments, change controls, investigations, and GMP documentation.

Responsibilities

• Lead PET technology transfer projects across the manufacturing network.
• Support new product onboarding, process implementation, and launches.
• Prepare, review, and approve tech transfer, validation, and GMP documentation.

Skills

Technology transfer

Pharmaceutical manufacturing

cGMP compliance

Technical writing

Project management

Education

Bachelor's degree in Chemistry, Pharmaceutical Sciences, Engineering, or related discipline

Advanced degree preferred

Job description

Jubilant Radiopharmacies is seeking a Project Scientist to support technology transfer, validation, and onboarding of new PET products across multiple sites. You will collaborate with Operations, Quality, Project Management, and external partners to ensure compliant implementation of processes.

Ideal candidates have 5+ years in tech transfer within pharma/radiopharma, strong technical writing, and project-management skills, with a focus on regulatory compliance and cross-site collaboration.