Quality Documentation Specialist

Curium Pharma; Maryland Heights (MO); On-site; USD 60,000 - 75,000; Full time

Job summary

Curium is seeking a Contractor Quality Documentation Specialist in Maryland Heights, MO to identify, scan, file and organize documentation supporting Quality, Regulatory Affairs, Research and Development.

Work schedule Monday through Friday 6:00 am to 2:30 pm. The role requires an Associate Degree or higher, one or more years of documentation experience in a cGMP facility, and strong MS Office and data-entry skills.

Qualifications

• Associate degree preferred.
• One+ years documentation in cGMP facility or medical transcription preferred.
• Proficient data entry and MS Office (Word, Excel, Access, Visio, Outlook, PowerPoint).
• Strong organization, time management and communication skills.

Responsibilities

• Catalog, scan, maintain, file and retrieve site documents.
• Maintain Quality Indices by updating Excel spreadsheets.
• Ensure safety, compliance to SOPs and regulatory guidelines.
• Maintain department, premises and equipment in good order.
• Comply with US and international regulatory agencies (FDA, ISO, etc.).

Skills

Data entry

Microsoft Office

Organization

Communication

Education

Associate Degree

High School Diploma

Job description

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(Contractor) Quality Documentation Specialist

Date: Aug 28, 2026

Location: Maryland Heights, MO, United States, 63043

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

This person will work with a small team responsible for identifying, locating, scanning, sorting and listing different types of documentation to support various departments including Quality, Regulatory Affairs, Research and Development.

Work Schedule: Monday - Friday 6am - 2:30pm

Essential Functions

• Catalog, scan, maintain, file, and retrieve various site documents.
• Maintain Quality Indices by accurately updating information in Excel spreadsheets.
• Ensure a safe and quality working environment through training, awareness, and compliance to safety guidelines and SOP’s.
• Ensure the maintenance of their department, premises and equipment.
• 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.).

Requirements

• Associate Degree preferred, High School Diploma or equivalent is required.
• One or more years of documentation experience in a cGMP facility or in the medical transcription field is preferred. Office administration experience will also be considered.
• Experience with computer data entry required. Must be proficient with Microsoft Office, including Word, Excel, Access, Visio, Outlook, and Power Point.
• Strong organization and time management skills, and good communication skills.

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 be able to work indoors and outdoors with exposure to mechanical/moving parts, hazards including corrosive, flammable and toxic material, dust, dirt, odors, and irritants.
• Willingness to complete safety training within allotted timeframes, and work in a team-based environment.
• Must be able to work outside of regular work hours, including off shift, weekend, and holiday work as business needs require.

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 anequal opportunity employerand believes everyone deserves respect, dignity and equality. All applicants will be considered for employmentwithout attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

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