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SOFIE

Sr. Radiochemist

Totowa, NJ · On-site

$90K - $100K/yr

... therapeutic radiopharmaceuticals for SOFIE within the Radiopharmaceutical Contract Manufacturing Division. Working closely with SOFIE's pharmaceutical partners, they will ensure that these ...

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How much do contract radiopharmaceuticals jobs pay per hour?

As of Jul 21, 2026, the average hourly pay for contract 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 the difference between Contract Radiopharmaceuticals vs Radiopharmacy Technicians?

AspectContract RadiopharmaceuticalsRadiopharmacy Technicians
CredentialsCertification in radiopharmacy, radiochemistry, or nuclear medicineCertification as a radiology or radiopharmacy technician often required
Work EnvironmentTemporary or project-based settings, hospitals, clinics, or research facilitiesHospital, clinic, or pharmacy settings with regular hours
Employer & Industry UsageContract roles for specific projects or coverageFull-time or part-time employment in healthcare facilities

Contract Radiopharmaceuticals professionals focus on specialized, temporary roles involving preparation and handling of radiopharmaceuticals, often working on specific projects. Radiopharmacy Technicians typically work in permanent positions within healthcare facilities, managing daily radiopharmaceutical preparation and distribution. Both roles require relevant certifications but differ mainly in employment type and work setting.

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What cities are hiring for Contract Radiopharmaceuticals jobs? Cities with the most Contract Radiopharmaceuticals job openings:
What are the most commonly searched types of Radiopharmaceuticals jobs? The most popular types of Radiopharmaceuticals jobs are:
What states have the most Contract Radiopharmaceuticals jobs? States with the most job openings for Contract Radiopharmaceuticals jobs include:
What job categories do people searching Contract Radiopharmaceuticals jobs look for? The top searched job categories for Contract Radiopharmaceuticals jobs are:
Contract Radiopharmaceuticals jobs near you
Infographic showing various Contract Radiopharmaceuticals job openings in the United States as of July 2026, with employment types broken down into 57% Full Time, 22% Part Time, 1% Temporary, and 20% Contract. Highlights an 79% Physical, 2% Hybrid, and 19% Remote job distribution, with an average salary of $107,964 per year, or $51.9 per hour.
Sr. Radiochemist

Sr. Radiochemist

SOFIE

Totowa, NJ • On-site

$90K - $100K/yr

Other

Re-posted yesterday

SOFIE rating

8.7

Company rating: 8.7 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

12th of 74 rated pharmaceutical

Job description

Sr Radiochemist, RCM Project Lead Reports To: Director, Radiopharmaceutical Contract Manufacturing (RCM) Compensation $90k - $100k Overview The Senior Radiochemist will lead the development, implementation, and validation of manufacturing and analytical methods of new diagnostic and therapeutic radiopharmaceuticals for SOFIE within the Radiopharmaceutical Contract Manufacturing Division. Working closely with SOFIE’s pharmaceutical partners, they will ensure that these radiopharmaceuticals are in full compliance with all regulatory requirements (specifically, 21 CFR 211 and 212). Essential Duties and Responsibilities Lead the development of protocols for the production and analysis of clinical/commercial-grade radiopharmaceuticals, validate these methodologies against quality requirements, and implement them for regular production of radiopharmaceuticals for preclinical or clinical use according to cGMP standards. It is expected that the development of these protocols will involve both the application of scientific principles and rationales and also adherence to regulatory requirements. Write clear Standard Operating Protocols (SOPs) for these protocols. Review existing SOPs and suggest logical modifications based on either scientific rationales and/or regulatory requirements. Serve as lead technical support and/or training for production staff at SOFIE sites, either remotely or on-site. Write corporate exception reports and other regulatory documents, such as risk assessments, change controls, etc. Conduct production or quality control analytical tests for regular production of radiopharmaceuticals for preclinical or clinical use according to cGMP standards. Install, qualify, and maintain laboratory equipment on site. Validate existing production or analytical methods on existing or new equipment. Lead the collaboration with other production radiochemists and quality control chemists as required to ensure successful protocol development and radiopharmaceutical production. Maintain all qualification and validation requirements for entering ISO classified areas. Maintain a clean and safe working environment and perform radiation safety duties in compliance with safety and pharmaceutical regulations. Maintain accurate radiopharmaceutical production records and test/validation results. Write reports, presentations, and other documentation summarizing experimental/production data. Coordinate with the Radiopharmaceutical Contract Manufacturing team’s activities to reach defined objectives. Liaise with our contract partners (e.g. biotech and pharma). Other duties as assigned. Qualifications Degree in chemistry, engineering or natural sciences preferred but will entertain applicants with relevant education and work experience. PhD preferred. 5 years’ experience preferred in radiopharmaceutical manufacturing and QC in a GMP or academic environment Expertise in laboratory procedures and analytical chemistry techniques required (thin layer chromatography, GC, HPLC, preparative HPLC, Radiometric Detectors, endotoxin, etc.). Experience with the use of automated synthesis modules and maintenance of automated modules required. Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals required. Knowledge of cGMP requirements, aseptic process (cleanroom environment), and equipment qualification preferred. Efficient in the use of MS Office Suite required. Ability to be detail-oriented, accountable, patient, organized, and work in a team environment with minimum supervision required. Strong technical writing skills required. Excellent organizational skills required. Ability to work various shifts and weekends required. Travel: up to 15 % domestically.

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