Manufacturing Technician - Cold Products
Listed on 2026-09-12
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Manufacturing / Production
Manufacturing & Industrial Operations, Production Associate / Production Line, Pharmaceutical Manufacturing, Medical Device Industry
Manufacturing Technician - Cold Products
Date:
Aug 28, 2026
Location:
Maryland Heights, MO, United States, 63043
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.
Performs all tasks associated with preparing, formulating and dispensing aseptically manufactured products in and ISO 5 cleanroom environment according to cGMP Guidelines in order to meet production demands.
Schedule:
Monday through Thursday
Weekend and off shift overtime as needed
- Ensure a safe and quality working environment through training, awareness, and compliance to safety guidelines, SOP's and FDA regulations.
- Responsible for following detailed instructions and communicating effectively, both written and verbally.
- Perform Batch Record calculations and maintain all documentation according to cGMP Guidelines.
- Set up, maintain, and clean appropriate equipment and work area according to SOP and in compliance with cGMP guidelines.
- Set up, operate, and monitor production equipment and processes in accordance with current good manufacturing practices and standard operating procedures.
- Calibrate or adjust equipment to ensure quality production, using internal calibration functions.
- Participate and perform effectively in a team environment and interact with multiple departments to ensure the operational success of the team.
- Responsibilities also include the ability to lift, reach, pull, and squat as needed, according to production demands.
- Adhere to all applicable regulations, policies, and procedures for health, safety, and environmental compliance.
- Troubleshoot problems with equipment, devices, or products.
- 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.).
- Associate Degree preferred, High school diploma or equivalent required.
- 1 or more years of manufacturing experience required (regulated environment, attention to detail and following detailed instruction).
- Knowledge of Good Manufacturing Practices c(GMP) and applicable Quality System Standards.
- Willingness to work rotating shifts, weekends, and overtime, as necessary.
- Effectively adjusts to changes and deals effectively with uncertainties in the workplace.
- Ability to generate new and valuable ideas and effective solutions to difficult problems; connects previously unrelated notions.
- Realizing the worth of all people and respects others, regardless of background or cultural differences.
- Thoroughly understanding the needs of internal/external customers and making customer satisfaction a top priority.
- Strong motivation and ability to achieve work goals and quantifiable business results.
- Ability and desire to cooperate, collaborate, and partner with others.
- Willingness to help outside your department and within your…
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