Data Integrity Specialist

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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.

We are seeking a contractor who will provide Data Integrity support for electronic and equipment systems at the Noblesville, IN facility.

Work Schedule:

Monday - Friday 8am - 4:30pm

• Review system documentation (e.g., user manuals, SOPs, validation reports)
• Conduct system assessments and inspections.
• Analyze audit trails for evidence of data manipulation, deletions, or unauthorized access.
• Review data for completeness, accuracy, and consistency.
• Assess data backup and recovery procedures.
• Evaluate user access controls and permissions.
• Compare current practices with data integrity requirements.
• Identify and remediate gaps and deficiencies.
• Prioritize identified gaps based on risk.
• The contract staff will document the assessment process, including findings, recommendations.
• Maintain current knowledge of federal and international data integrity regulations
• Manage and prioritize project in an organized and structured manner
• Maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EP, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.)
• Complete Periodic Reviews of equipment.
• All other responsibilities as assigned with or without accommodation.

• Bachelor Degree preferred. Work experience is considered in lieu of degree.
• Three or more years of relevant work experience understanding and interpreting cGMP, GLP or GCP regulations with a focus on Data Integrity requirements
• Candidates must understand how to apply regulations within manufacturing and laboratory environments.
• Experience reviewing / authoring standard operation procedures.
• Proficiency with core computer software / systems (Microsoft Word, Excel, SharePoint, Project, etc.)

Working Conditions:

• 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 include the ability to lift up to 70 pounds, kneeling, crouching, twisting the upper body, walking, bending, stooping, pushing, pulling, reaching, must be able to physically negotiate stairs and evacuation ladders with or without accommodation, wear and operate safety equipment, enter vessels, and inspect equipment.
• Material handling devices (e.g., hand truck, fork truck, and conveyors) are used when possible, however, use of proper lifting and movement techniques is necessary to prevent injury.
• Must be willing to wear a variety of Personal Protective Equipment (PPE) and hearing protection as needed.
• May be required to sit or stand for long periods of 8+ hours a day while performing duties.
• Must possess good hand-eye coordination; close attention to detail is required.
• Must…