Nuclear Pharmacist I

SOFIE Co.; Kansas City (MO); On-site; USD 90,000 - 130,000; Full time

Job summary

JobRx, Inc. is seeking a Nuclear Pharmacist I to compound and dispense radiopharmaceuticals in a clean room, with exposure to radiation. This role supports the Quality Assurance Program and collaborates with site QA staff to ensure regulatory compliance.

The position requires state licensure, nuclear pharmacy background, and ability to work varied shifts, including weekends, with travel up to 10%. MS Office proficiency and experience with Pinestar are preferred.

Qualifications

• Requires degree in pharmacy (B.S. or Pharm.D.) and active licensure in good standing.

Responsibilities

• Compound and dispense radiopharmaceuticals in a clean room.
• Perform synthesis, QC, and QA for FDG and NaF.
• Ensure compliance with USP 797/823 and FDA regulations; maintain SOP adherence.
• Prepare and review cGMP docs; assist QA with investigations, CAPAs, deviations, and records.
• Review and release batch records with QA; support change controls.
• Train and supervise nuclear pharmacy technicians; participate in meetings.

Skills

Attention to detail

Teamwork

Regulatory compliance

Communication

Problem solving

Quality mindset

Education

B.S. or Pharm.D. from an accredited pharmacy school

Nuclear pharmacy certification (preferred)

State license required (to be obtained post-hire if applicable)

Tools

MS Office

Pinestar or pharmacy applications

Job description

Nuclear Pharmacist I

Department: Network Operations, Pharmacy

Reports To: Pharmacist-in-Charge and Facility Manager

Overview

The Nuclear Pharmacist I will compound and dispense radiopharmaceuticals. This job involves working in a clean room as well as occupational exposure to radiation. While reporting into Network Operations, the Nuclear Pharmacist role is instrumental to the Quality Assurance Program within SOFIE and will work closely with the QA division at the site-level.

Essential Duties and Responsibilities

• Perform the duties associated with compounding, dispensing, and distribution of radiopharmaceuticals, including data entry with Pinestar for end‑of‑day reports and daily dose management reports.
• Perform the duties associated with synthesis, quality control, and quality assurance of FDG and NaF, including reagent preparation.
• Ensure compliance with USP <797>, <823>, proposed <825> regulations, or other state pharmacy requirements as applicable, at the site level; maintain personal license in good standing through applicable state laws.
• Ensure compliance to all applicable standard operation procedures (SOPs) and regulations, including 21 CFR Parts 211 and 212 requirements, by adhering to SOFIE's quality management system and maintain a state of cGMP control at the site.
• Ensure aseptic operations follow internal procedures (gowning, cleaning/sanitation, sterility, environmental monitoring, etc.), customer requirements, and FDA regulations.
• Ensure compliance with radiation and laboratory safety of the site, including the ability to address chemical or radioactive spills and reporting.
• Complete cGMP documents as required and assist site and corporate Quality Assurance including, but not limited to:
  • Investigations
  • Corrective and Preventative Actions
  • Deviations
  • Out of Specifications
  • No or Atypical Yields
  • Manufacturing and QC Records
  • Logbooks
• Write and review internal procedures.
• With site QA, review and release batch records as applicable.
• Responsible for opening change controls and initiating, maintaining, and reviewing SOFIE network and site specific procedures relative to their job functions.
• With site QA, monitor the metrology program at the site. Ensure that equipment is appropriately maintained, calibrated/recalibrated, or validated/revalidated in a timely manner.
• With site QA, monitor customer/patient complaints to determine the possible root causes. Work with the customers to ensure their concerns are addressed, quality standards are met, and issues are resolved promptly and effectively.
• Provide on‑floor QA oversight of manufacturing, QC, and other cGMP activities. Identify non‑compliance problems and propose solutions. Effectively interact with other functional personnel and resolve quality related issues on the spot whenever possible.
• Provide quality customer service associated with radiopharmaceuticals to physicians, healthcare workers, customers, etc. as needed.
• Train and supervise nuclear pharmacy technicians and maintain accurate training records.
• Attend corporate and site level meetings as applicable.
• Perform other duties as assigned.

Qualifications

• B.S. or Pharm.D. from an accredited pharmacy school required; nuclear certification preferred.
  • State license required (to be obtained post‑hire if applicable).
  • Background in nuclear pharmacy, Positron Emission Tomography, radiation safety and/or familiarity with cyclotron processes preferred.
• Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations required.
• Ability to write reports, business correspondence, and procedure manuals required.
• Ability to effectively present information and respond to questions or complaints from groups of managers, clients, customers, the public required, or regulatory agencies required.
• Ability to define problems, collect data, establish facts, and draw valid conclusions required.
• Strong management and interpersonal skills required.
• Proficient in all MS Office applications required. Proficiency in Pinestar or other pharmacy applications preferred.
• Ability to be detail‑oriented, responsible, dependable, patient, organized, professional and work in a team environment required.
• Ability to work various shifts and weekends required.
• Ability to communicate professionally with colleagues and customers, have excellent attention to detail, and be dependable and responsible in a fast‑paced, highly technical environment required.
• Ability to lift ~50 lbs required.
• Up to 10% travel required.