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 Quality Control Technician

St Louis, MO
  • Overview

    Perform assigned laboratory testing and related quality control activities in order to ensure compliance with applicable SOP’s and cGMPs. Provide timely testing and notification of any aberrant occurrence to Management / Supervision that presents potential negative impact to manufactured or marketed product. Work under limited supervision with considerable latitude for the use of initiative and independent judgment. Must have good documentation skills.

  • Responsibilities

    • Ensure a safe and quality working environment through training, awareness, and compliance to Safety/Quality guidelines and SOPs.
    • Ensure the maintenance of their department, premises, and equipment.
    • Ensure that all necessary training is carried out to perform all the assigned tasks confidently and consistently.
    • Perform all work in compliance with site safety and radiation protection guidelines.
    • Collaborate with other team members to ensure that quality tasks are performed in a timely manner.
    • Must demonstrate flexibility in adjusting to changing priorities and schedules.
    • Attend mandatory trainings as required by site regulatory requirements and management.
    • Assist with investigations by providing testing results and communication of practice(s).
    • Assist in the training and development of employees.
    • Perform other general duties associated with the position as required by supervision.

  • Qualifications

    • Associate Degree in Life Sciences or a related field or completion of four college-level life science courses required. Bachelor Degree in life science or a related field preferred.
    • Three or more years of general quality / quality control / production experience in a cGMP facility required.
    • Proficient in the use of several of the following laboratory instruments: Analytical Balance, pH meter, automatic pipettes, FTIR, UV-Vis, Voltammeter, Autotitrator, HPLC, GC, IC, ICP, Flame AA, TOC, Conductivity meter.
    • Willing to edit, modify and create cGMP documents
    • Ability to work independently and with others to accomplish goals and priorities.

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