Redefining the experience of cancer through our trusted legacy in nuclear medicine

Pharmaceutical Manufacturing

Nuclear Medicine, PET Imaging, Molecular Imaging, cGMP Manufacturing , Contract Manufacturing, and SPECT Imaging


Paris, France



Curium is the global leader in nuclear medicine, providing life-changing diagnostics and treatment to patients all over the world. We develop, manufacture and distribute world-class radiopharmaceutical products with a renewed focus on cancer, exploring untapped potential for new innovation. We build on remarkable foundations and a legacy of providing reliable and consistent nuclear solutions to tens of thousands of patients every day. Our proven heritage combined with a pioneering approach are the hallmarks from which we provide life-changing diagnostics and therapeutics. Our people are the root of the incredible impact they have. We strive to make the impossible possible and to be an organization that will change the face of medicine. Our diverse group of industry experts is unified under one strong and singular focus – to develop, manufacture and supply revolutionary diagnostic and therapeutic radiopharmaceuticals to our customers around the globe with unrivaled reliability and superior service.
Video - The Curium Way

The Opportunity

Senior Manufacturing Technician - Contract

St Louis, MO
  • Overview

    The role of a Senior Manufacturing Technician is to perform all tasks associated with operating equipment through formulation, preparation, and dispensing of aseptic fill radiopharmaceutical processes, according to cGMP guidelines to meet production demands. The Senior Manufacturing Technician will work with advanced automated equipment, in the creation of new products, and serve as one of several lead technicians while coordinating work in accordance with standard operating procedures (SOP’s).

  • Responsibilities

    • Sunday – Thursday (5 eight-hour shifts per week).

    • Work Hours: 6:00 AM to 2:30 PM.

    • Ability to work overtime when necessary.

    • Demonstrates an ability to provide directional leadership on the floor.

    • Follows quality, safety, regulatory guidance’s and written procedures.

    • Is an active member with continuous improvement.

    • Ensures the maintenance and cleanliness of department, premises and equipment.

    • Performs documentation in accordance with cGMP guidelines.

    • Properly reviews Batch Records.

    • Works with team to drive team environment.

    • Follows all written procedures and verbal instructions.

    • Communicates effectively through written or spoken instructions.

    • Takes full ownership and accountability of process.

    • Works with coordinator to resolve challenges.

    • Works with leadership to improve operations.

    • Must be willing to attend additional training/schooling when required.

    • Ensures internal / external customer expectations are met or exceeded.

    • Capable of adjusting to changes and dealing effectively with uncertainties in the workplace.

    • Drives to achieve work goals and quantifiable business results.

    • Collaborative attitude for business success.

    • Demonstrates willingness to be flexible to the needs of the department and business.

  • Qualifications

    • Associate Degree or completion of an equivalent certification program from a technical or vocational school is required. Equivalent relevant years of experience in this field of study will also be considered.
    • Three to five years of relevant work experience is required, preferably in a pharmaceutical or manufacturing industry.
    • Experience working in an FDA-regulated cGMP environment is preferred.
    • Strong mechanical aptitude is required, scientific background is preferred.
    • Must be capable of providing front line troubleshooting of manufacturing equipment and process issues, properly elevating concerns and issues to appropriate personnel.
    • Willingness to work in plant producing radioactive materials and requiring all employees to participate in safety programs designed to minimize potential and/or actual exposure levels.
    • Responsibilities also include the ability to lift up to 70 pounds, walk, bend, stoop, kneel, crouch, crawl, twist upper body, push, pull, reach, and climb stairs and ladders with or without accommodation.
    • Must be willing to wear a variety of personal protective equipment.
    • May be required to sit or stand for long periods of time while performing duties.
    • Must be able to work outside of regular work hours, work rotating shifts, weekends, and overtime, as necessary.
    • Willingness to work around mechanical and moving parts, around low and high voltages, with exposure to dust, dirt, odors and irritants.
    • Close attention to detail is required and must possess good hand-eye coordination.
    • Willingness to work in a team-based environment.

Building career-spanning relationships, from candidacy to organizational leadership, we provide access to the future of the Medtech and Pharma.