ABOUT CURIUM

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 are the hallmarks to deliver innovation, excellence and unparalleled service.
With manufacturing facilities across Europe and the United States, Curium delivers SPECT, PET and therapeutic radiopharmaceutical solutions for life-threatening diseases to over 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 emphasizes our focus on nuclear medicine. The tagline ‘Life Forward’ represents our commitment to securing a brighter future for all those we serve: An enhanced quality of care for our patients. A trusted partner to our customers. A supportive employer to our valued team.

SUMMARY OF POSITION

The Manufacturing Technician in Cyclotron Chemistry position produces the Active Pharmaceutical Ingredient for cyclotron-based radiopharmaceuticals through purification of starting materials by means of chemical processing. This work is conducted in cGMP and NRC compliant laboratories utilizing advanced equipment.
Work Schedule: Saturday through Wednesday 1030-1900. Ability to work overtime when necessary.

REQUIREMENTS

• Associate Degree or completion of an equivalent certification program from a technical or vocational school is preferred. High school diploma or equivalent is required.
• Knowledge of Good Manufacturing Practices c(GMP) and experience working in a FDA regulated cGMP environment is desired.
• 1 or more years of relevant work experience required.

• Ensure a safe and quality working environment.
• Awareness of FDA, NRC, ALARA, and OSHA requirements.
• Work according to SOPs and cGMP guidelines.
• Train and qualify on the manufacturing processes of the area.
• Start up and shut down processing equipment.
• Ensure proper maintenance and cleanliness of equipment.
• Become proficient with using tele-manipulators.
• Perform proper line clearances.
• Properly record data per SOPs and cGMP guidelines.
• Perform Batch Record calculations.
• Work within the team environment and interact with other departments for operational success.
• Accurately count materials and labels.
• Accurately label products.
• Use logical methods to solve problems with effective solutions and make quick quality decisions.
• Assist and support in investigations and process improvements.
• Participate in safety programs, committees, or teams.
• Prepare chemical solutions for processes, following standardized formulas.
• Follow both spoken and written directions.
• Communicate effectively, both written and verbally.
• Perform duties as assigned by leadership.
• Wiliness to be flexible and adaptable to the needs of the department and business.
• Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.).