The African Medical Centre of Excellence (AMCE) Abuja Job Vacancy-Cyclotron Radio Pharmacist

Job Title: Cyclotron Radio Pharmacist

Location: Abuja, Nigeria
Employment Type: Full Time
Workplace Type: Onsite

Job Purpose

• The Cyclotron Radiopharmacist will be responsible for providing strategic leadership and technical oversight for all cyclotron and radiopharmacy operations, ensuring the safe, efficient, and regulatory-compliant production of high-quality radiopharmaceuticals.
• This role is pivotal in supporting advanced diagnostic imaging by guaranteeing the consistent availability of pure and effective radiotracers for nuclear medicine procedures.
• The role holder will manage production schedules, enforce stringent quality control measures, lead a team of radiopharmacy professionals, and uphold the highest standards of radiation safety and regulatory compliance, ultimately contributing to exceptional patient care and clinical outcomes.
  Key Accountabilities/Responsibilities
  Radiopharmaceutical Production & Operations Management:
  • Manage and oversee the entire production process of radiopharmaceuticals, ensuring strict adherence to established synthesis protocols and safety standards.
  • Optimize daily production schedules to efficiently meet clinical demand and implement sterile compounding techniques and aseptic conditions.
  • Lead the planning and execution of cyclotron operations, including target preparation, irradiation, and target processing.
  • Develop and implement departmental Standard Operating Procedures (SOPs) for all aspects of radiopharmaceutical production.

  Quality Assurance & Regulatory Compliance

  • Implement and monitor comprehensive quality control measures to ensure the safety, efficacy, purity, and potency of all radiopharmaceuticals.
  • Develop and validate robust analytical methods for the testing and characterization of radiopharmaceutical batches.
  • Ensure 100% compliance with all local and international regulations (e.g., NAFDAC, IAEA, pharmacopoeial standards) and prepare for regulatory inspections and audits.
  • Investigate and resolve any out-of-specification (OOS) results or deviations and lead continuous quality improvement initiatives.

  Equipment Management & Maintenance

  • Oversee maintenance and calibration programs for the cyclotron and all associated radiopharmacy equipment (e.g., synthesis modules, dose calibrators, analytical instruments).
  • Develop and implement robust preventative maintenance schedules to ensure optimal performance, reliability, and longevity of all critical equipment.
  • Coordinate with external service providers for specialized equipment repairs, certifications, and compliance testing.
  • Evaluate and recommend the acquisition of new radiopharmacy equipment and technologies.

  Research, Innovation & Interdisciplinary Collaboration

  • Actively participate in research initiatives to develop novel radiopharmaceuticals and explore new applications, collaborating on clinical trials.
  • Stay updated on the latest  scientific advancements in radiochemistry, nuclear medicine, and pharmaceutical  sciences.
  • Collaborate closely with nuclear medicine physicians, technologists, and other departments to optimize imaging protocols and patient care.
  • Liaise with regulatory agencies, procurement teams, and senior management to ensure seamless operations and strategic alignment.

  Qualifications

  • Doctor of Pharmacy (Pharm.D.) or Master’s/PhD in Radiopharmacy, Radiochemistry, Pharmaceutical  Sciences, or a closely related field.
  • Formal training and certification in Good Manufacturing Practice (GMP) , Good Radiopharmacy Practice (GRPP) , and radiation safety is highly preferred.
  • Eligibility to act as a Qualified Person for radiopharmaceuticals is a distinct advantage.
  • 5 – 7 years of progressive experience in a clinical or research radiopharmaceutical environment, with direct, hands-on experience in cyclotron operations and radiopharmaceutical production.
  • Demonstrated, in-depth expertise in the GMP-compliant production and quality control of radiopharmaceuticals for PET imaging.
  • Proven experience in leading teams, managing operational schedules, and developing SOPs within a regulated environment.
  • Expert knowledge of analytical techniques (HPLC, TLC, gamma-ray spectrometry) and sterile compounding.
  • Strong track record in regulatory compliance, audits, and meticulous documentation.
  • Experience in research, development, and validation of novel radiopharmaceuticals is a distinct advantage.
  • Excellent communication, leadership, and interpersonal skills.

  Application Closing Date
  Not Specified.

  How to Apply
  Interested and qualified candidates should:
  Click here to apply online

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