Quality Documentation Specialist — Reg & Data Entry

Curium Pharma; Maryland Heights (MO); On-site; USD 25,000 - 33,000; Part time

Job summary

Curium Pharma in Maryland Heights, MO is seeking a contracted Quality Documentation Specialist to support Quality, Regulatory Affairs and R&D by identifying, scanning, sorting and listing various documentation.

Working schedule is Monday to Friday, 6am to 2:30pm. You will catalog, scan, file and retrieve site documents and maintain Quality Indices in Excel while ensuring compliance with safety, SOPs, and global regulatory guidelines.

Qualifications

• Associates preferred; high school diploma required.
• 1+ year of documentation experience in cGMP or medical transcription preferred.
• Experience with Microsoft Office Suite required (Word, Excel, Access, Visio, Outlook, PowerPoint).
• Strong organization, time management and communication skills.

Responsibilities

• Catalog, scan, file, and retrieve site documents.
• Maintain Quality Indices by updating Excel spreadsheets.
• Ensure safety and quality through training, SOP compliance, and regulatory guidelines.
• Maintain department, premises and equipment.
• Ensure operational compliance with FDA, EU, ISO, NRC, and other guidelines.

Skills

Organization

Time management

Communication

Education

Associate Degree

High School Diploma

Tools

Microsoft Word

Microsoft Excel

Microsoft Access

Microsoft Visio

Microsoft Outlook

PowerPoint

Job description

Curium Pharma in Maryland Heights, MO is seeking a contracted Quality Documentation Specialist to support Quality, Regulatory Affairs and R&D by identifying, scanning, sorting and listing various documentation.

Working schedule is Monday to Friday, 6am to 2:30pm. You will catalog, scan, file and retrieve site documents and maintain Quality Indices in Excel while ensuring compliance with safety, SOPs, and global regulatory guidelines.