Back to Job SearchROLE OVERVIEW
We are currently looking for a Radiopharmacy QC Specialist to join a leading provider of nuclear medicine solutions based at a prominent healthcare facility. This is an exciting opportunity for a dedicated professional with solid radiopharmacy experience to contribute to a state-of-the-art facility committed to delivering life-saving radiopharmaceuticals to patients worldwide. The role offers a fixed-term contract of two years, with full-time, on-site shifts, supporting the delivery of high-quality products within a GMP compliant environment.
Joining our client means becoming part of a pioneering company with a rich heritage in nuclear medicine. You will play a vital role in ensuring quality standards are met, supporting validation activities, and training technicians, all while working within a collaborative, innovative team focused on improving patient care.
KEY DUTIES AND RESPONSIBILITIES
Your duties as the Radiopharmacy QC Specialist will be varied; however, the key duties and responsibilities are as follows:
- Oversee and maintain GMP compliance within the QC laboratory, reviewing analytical and production methods to ensure adherence to industry regulations and guidelines.
- Perform, review, and document QC tests and microbiological results, managing out-of-specification (OOS) results and investigations.
- Support the review and approval of deviations, investigations, CAPA, change controls, and ensure all quality records are accurately maintained and updated.
- Assist in the training of technicians in QC analytical testing for SPECT and PET radiopharmaceuticals, ensuring protocols are followed correctly.
- As the QC Specialist, you will ensure all activities are conducted in full accordance with GMP, update SOPs, and support validation and calibration processes.
ROLE REQUIREMENTS
To be successful in your application to this exciting role as the Radiopharmacy QC Specialist, we are looking to identify the following on your profile and past history:
- A Degree or higher level in a related scientific field (e.g., Pharmaceutical Chemistry, Radiopharmacy, Quality Assurance, or Quality Management).
- Proven 2-3 years of radiopharmacy experience in quality control environments, with working knowledge of pharmaceutical chemistry and good manufacturing practices.
- Practical experience with GMP compliance, documentation management, and QC testing methodologies.
- Excellent attention to detail, communication skills, and the ability to work effectively within a team.
WHAT’S IN IT FOR YOU?
This role offers the chance to work in a cutting-edge environment dedicated to advancing nuclear medicine and improving patient outcomes. You will be part of a reputable organization committed to innovation and excellence, with opportunities to develop your expertise in radiopharmaceutical quality control. The position also provides a competitive salary package and the chance to contribute to life-changing medicines globally.
Key Words: Radiopharmacy / Quality Control / GMP / QC Testing / Validation / Documentation / Radiopharmaceuticals / Microbiology / CAPA / Deviation / Audit / Training / Pharmaceutical Chemistry / Good Manufacturing Practice
"Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career."
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
