(Contractor) Quality Control Technician Job Details | curium

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 (Contractor) Quality Control Testing Engineer role is responsible for performing analytical testing of raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with regulatory and company standards. This role is critical to maintaining product quality, supporting production timelines, and ensuring regulatory compliance.

Work schedule : Monday Friday 8am 4 : 30pm

Essential Functions

• Perform routine and non-routine analytical testing using techniques such as HPLC, GC, UV-Vis, FTIR, titration, ICP-MS etc.
• Conduct testing on raw materials, intermediates, and finished products in accordance with cGMP and SOPs.
• Review and interpret analytical data; prepare detailed and accurate reports and documentation.
• Maintain laboratory equipment, including calibration, qualification, and troubleshooting.
• Participate in method development, method validation, and stability studies as required.
• Ensure compliance with all applicable regulatory requirements (e.g., FDA, EMA, ICH) and internal quality standards.
• Support investigations (OOS, OOT, deviations) and assist in root cause analysis and CAPA implementation.
• Maintain a clean and organized laboratory environment and adhere to safety guidelines.
• Participate in audits and inspections and support documentation requests from regulatory authorities.
• Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, DEA, EU, HC, TGA, PIC / S, ISO, USP, NRC, cGMP, etc.).

Requirements

Working Conditions :

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.

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