Manager Quality Control Technical Services

Manager Quality Control Technical Services

Date:
Aug 4, 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.

The Manager Quality Control Technical Services (QCTS) is responsible for the end‑to‑end lifecycle management of QC laboratory instruments and related computerized systems, including qualification, calibration, maintenance, change control, and decommissioning within a GMP environment. This position oversees the Maryland Heights, MO, and Noblesville, IN sites and manages three direct reports at the Maryland Heights facility and one direct report at the Noblesville, IN facility.

• Oversight of Preventative Maintenance and Demand Maintenance on QC instruments and equipment.
• Manages outside service providers and service contracts to support preventive maintenance, repair activities, qualification services
• Author/Approve analytical method, and equipment/instrument IQ/OQ/PQ protocols, Standard Operating Procedures, Change Controls, etc.
• Ensuring computerized systems and analytical data remain compliant with data integrity expectations.
• 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.).
• Author Change Controls, Protocols, Corrective and Preventive Action items and Periodic Reviews.
• Assure compliance with department training and qualification.
• Work safely with radioactivity and ensure all direct reports maintain ALARA and manage their daily activities accordingly to ensure they meet their quarterly ALARA goals.
• Provides technical counsel concerning the scientific content of methods, analytical testing of samples, evaluation and interpretation of laboratory results, and other QC related issues as required.
• Authors Change Controls in Quality Management systems.

• Bachelor of Science Degree in Chemistry, or other science related field, preferred.
• Twelve or more years of experience in QC laboratory operations, analytical instrumentation, or technical services in a regulated environment required.
• Two or more years of supervisory experience required.
• Strong knowledge of GMP, data integrity, calibration, qualification, and equipment lifecycle management.
• Experience managing outside vendors, maintenance providers, and service contracts.
• Demonstrated ability to author and review SOPs, protocols, reports, and technical documentation.
• Experience supporting deviations, CAPAs, change controls, investigations, and audits.
• Strong project management, problem‑solving, and cross‑functional collaboration skills.
• Familiarity with computerized systems and analytical data platforms used in QC laboratories.
• Ability to prioritize multiple projects and support instrument uptime in a fast‑paced…