Radiopharmacy Technician

Curium Pharma; Oxford; On-site; GBP 30,000 - 45,000; Full time

Job summary

Curium Pharma, located in Oxford, is seeking a Radiopharmacy Technician to support the build, validation, and operation of a PET Radiopharmacy facility. This role involves hands-on GMP production and quality control of PET radiotracers for clinical use.

The ideal candidate will have experience in GMP environments, strong attention to detail, and the ability to work effectively in a team. We offer opportunities for development within a pioneering nuclear medicine company.

Qualifications

• Contribute technical expertise during facility build, installation, and commissioning.
• Perform QC testing and maintain GMP-compliant documentation.
• Assist with equipment qualification and requalification activities.

Responsibilities

• Manufacture PET radiopharmaceuticals using hot cells and isolators.
• Conduct environmental and radiation monitoring.
• Manage incoming materials and stock levels.

Skills

Technical expertise in facility build

Attention to detail

Communication skills

Ability to work independently

Teamwork skills

Education

Experience in controlled or GMP environments

Working knowledge of pharmaceutical chemistry

Job description

Curium is the world’s largest nuclear medicine company with more than a century of industry experience. We develop, manufacture, and distribute world‑class radiopharmaceutical products to help patients around the globe. Our proven heritage, combined with a pioneering approach, is the hallmark of delivering innovation, excellence, and unparalleled service.

Join Us as a Radiopharmacy Technician!

We are looking for a talented professional to join our team supporting the build, validation, and operation of a PET Radiopharmacy facility, followed by hands‑on involvement in GMP production and quality control of PET radiotracers for clinical use.

From early project phases through full GMP operations, you will play a key role in ensuring safe, compliant, and high‑quality radiopharmaceutical production.

What You’ll Do:

Project & Validation Phase

• Contribute technical expertise during facility build, installation, and commissioning
• Assist with equipment, production, and QC validation activities

PET Radiopharmaceutical Production

• Manufacture PET radiopharmaceuticals using hot cells and isolators
• Perform sterile and aseptic dispensing using negative pressure isolator technology
• Apply radiation protection principles (ALARA) at all times
• Support packing and dispatch in line with transport and regulatory requirements

Cleanroom & Facility Operations

• Perform sanitation and cleaning of aseptic suites, isolators, and production areas
• Conduct environmental and radiation monitoring
• Manage consumables transfer and stock control

Quality Control & GMP Compliance

• Perform QC testing (radiochemical and radionuclide purity) per European Pharmacopoeia
• Maintain GMP‑compliant documentation and batch records
• Support deviation management, Root Cause Analysis, and CAPA activities
• Assist with equipment qualification and requalification activities
• Manage incoming materials, stock levels, and system production orders
• Maintain equipment and facility logs (fridges, freezers, isolators, etc.)
• Support the training of technicians across the PET manufacturing and QC processes
• Work cross‑functionally to ensure smooth production and quality operations
• Working knowledge of pharmaceutical chemistry and GMP
• Experience working in controlled or GMP environments
• Strong attention to detail and documentation discipline
• High level of computer literacy
• Strong communication and teamwork skills
• Ability to work independently and manage priorities effectively
• Willingness to work rotating 12‑hour shifts (midnight – 17:00 window)

Nice to Have

• Radiopharmacy or aseptic dispensing experience
• Knowledge of Ionising Radiation Local Rules, COSHH, and H&S procedures

Disclaimer

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of employees assigned to this position.

Equal Opportunity Employer

Curium is an equal‑opportunity employer and believes everyone deserves respect, dignity, and equality. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.