SP HRF Laboratory Technician

Description

Position Summary: As a laboratory technician, you will prepare and perform quality control of radiopharmaceuticals, ensuring traceability, managing waste, and complying with radiation protection regulations and Good Manufacturing Practices (GMP). Key Responsibilities: 1. Preparation and quality control of radiopharmaceuticals 2. Ensuring traceability of radiopharmaceuticals and waste management 3. Compliance with radiation protection regulations and Good Manufacturing Practices (GMP) **About Curium** Curium is the world’s largest nuclear medicine company, with over a century of experience in the industry. We develop, manufacture, and distribute high-quality radiopharmaceutical products to help patients worldwide. Our proven legacy, combined with a pioneering approach, defines our commitment to innovation, excellence, and unparalleled service. With manufacturing facilities across Europe and the United States, Curium provides SPECT, PET, and therapeutic radiopharmaceutical solutions for life-threatening diseases to more than 14 million patients annually. The name ‘Curium’ honors the legacy of pioneering radioactive researchers Marie and Pierre Curie—after whom the radioactive element curium was named—and underscores our focus on nuclear medicine. The motto ‘Life Forward’ reflects our commitment to securing a brighter future for all those we serve: better quality of care for our patients; a trusted partner for our customers; and an employer supporting our valuable team. **Summary of Position** ----------------------- As a laboratory technician, your mission will be to carry out radiopharmaceutical preparation and quality control operations, and all related activities, under the supervision of the Responsible Radiopharmacist/Coordinator. **Essential Functions** ----------------------- * Preparation of radiopharmaceuticals on time and according to specifications. * Quality control of preparations according to specifications. * Cleaning of the work area according to specifications. * Reporting on required activities. * Ensuring traceability of all radiopharmaceuticals. * Waste management. * Compliance with radiation protection rules and Good Manufacturing Practices (GMP) applicable to extemporaneous radiopharmaceutical preparation. * Proposing modifications to procedures. * Reviewing and issuing Quality Assurance System documents. * Recording non-conformities and customer complaints. * Reporting on raw material stock levels and order status and activities. * Order stock control and consumables control. * Implementing and collaborating in the implementation of the facility’s MVC Plan. * Performing facility operations in accordance with facility procedures and instructions, as well as supervisor directives. * Notifying the supervisor in case of emergency. **Requirements** ---------------- * Higher Technician Diploma in Diagnostic Imaging and Nuclear Medicine, or equivalent qualification with strong affinity for technical subjects. * Training in Good Manufacturing Practices (GMP) and sterile drug manufacturing. * License to operate in radioactive facilities. * Results-oriented. * Capable of working independently. * Teamwork skills. **Competencies** ---------------- **Disclaimer** The above statements are intended to describe the general nature and level of work performed by employees assigned to this classification. They should not be interpreted as an exhaustive list of all responsibilities, duties, and skills required of employees assigned to this position. **Equal Employment Opportunity** Curium is an equal opportunity employer and believes that everyone deserves respect, dignity, and equality. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.