Documentation Systems Specialist III Virginia Economic Development Partnership · Charlottesville, VA 09/07/2026

Moss Interactive, LLC; Charlottesville (VA); On-site; USD 34,000 - 48,000; Full time

Job summary

Afton Scientific is seeking a Documentation Systems Specialist III to join our Quality Assurance team in Charlottesville. You will manage master documents, batch records, SOPs, and change controls, ensuring accuracy and regulatory compliance.

Responsibilities include administering MasterControl or Veeva, supporting audits, and coordinating document changes with cross-functional teams. Candidates should have a Bachelor's degree or 5+ years in pharmaceutical documentation and strong communication

Qualifications

• Bachelor's degree or minimum five years in pharmaceutical administration, documentation, or related role.
• General experience in biopharmaceutical production or Quality Control.
• Knowledge of cGMP and FDA/EU guidance for aseptic processing.
• Experience with GMP-compliant document management systems (MasterControl/Veeva).
• Advanced MS Word and Excel; ability to learn new database apps.
• Strong written and verbal communication; detail-oriented.

Responsibilities

• Manage and administer documentation systems (SOPs, batch records, specifications, change controls).
• Notify stakeholders of document changes and maintain change-tracking records.
• Assign lot numbers and issue batch records; write and edit master documents.
• Review and approve Change Control documentation and Operational Deviation Reports as applicable.
• Support audits and VIP visits by facilitating documentation requests.
• Provide general admin support and cross-functional assistance as qualified.

Skills

Attention to Detail

Documentation

Data Integrity

Quality & Regulatory Compliance

Organization

Communication

Problem Solving

Stakeholder Support

Education

Bachelor's degree or 5+ years experience

Tools

MasterControl

Veeva

GMP Document Management System

Job description

Virginia Economic Development Partnership

Charlottesville, VA Full Time Manufacturing and Production

Afton Scientific is seeking an experienced, detail-oriented Documentation Systems Specialist III to join our Quality Assurance team. This position plays an important role in maintaining the integrity, accuracy, and control of Afton's documentation systems while supporting our pharmaceutical manufacturing and quality operations.

Compensation

• $25.00 – $35.00 per hour

Placement within the range will be based on qualifications, relevant experience, internal equity, and demonstrated competencies.

Primary Responsibilities

• Support the overall administration and management of Afton's Documentation Systems.
• Maintain master lists and approved controlled documents, including SOPs, directives, policies, batch records, protocols, and specifications.
• Notify clients and appropriate stakeholders of changes to controlled documents.
• Maintain records of approved change requests and investigation documentation.
• Assign lot numbers and issue batch records.
• Issue validation protocols for execution and process completed protocols following closure.
• Write, review, and edit master documents, including SOPs, batch records, and specifications.
• Review and approve Operational Deviation Reports (ODRs) and Change Control documentation, as applicable.
• Support audits and pharmaceutical VIP visits by facilitating documentation requests.
• Provide general administrative support as assigned.
• Provide inspection support to Finishing Operations, as qualified.
• Maintain positive and professional working relationships with coworkers, internal customers, and vendors.

Minimum Qualifications

• Bachelor's degree or a minimum of five years of experience in pharmaceutical administration, documentation, or a related role.
• General experience within biopharmaceutical production or Quality Control.
• Comprehensive knowledge of cGMP requirements and applicable FDA and EU guidance related to aseptic processing.
• Experience using a GMP-compliant document management system, such as MasterControl, Veeva, or a comparable platform.
• Advanced computer skills, including Microsoft Word and Excel, with the ability to learn additional database applications.
• Strong written and verbal communication skills.
• Ability to maintain accurate records and manage documentation with a high degree of attention to detail.
• Ability to work effectively with minimal supervision.

Preferred Knowledge and Experience

• Experience administering controlled documentation within a pharmaceutical or biopharmaceutical environment.
• Experience with MasterControl, Veeva, or another electronic document management system.
• Experience working with SOPs, batch records, specifications, protocols, and other GMP-controlled documents.
• Familiarity with Change Control and Operational Deviation processes.
• Experience supporting internal, client, or regulatory audits.
• Experience working cross-functionally with Quality Assurance, Quality Control, Operations, and other departments.

Key Competencies

• Attention to Detail & Accuracy
• Documentation & Data Integrity
• Quality & Regulatory Compliance
• Organization & Prioritization
• Communication & Collaboration
• Accountability & Follow-Through
• Independent Problem Solving
• Customer & Stakeholder Support

What You'll Gain

• Increased exposure to Afton's Quality Management System and controlled-document processes.
• Experience supporting documentation critical to pharmaceutical manufacturing, validation, and Quality Assurance.
• Opportunities to work across departments and support audits, investigations, change controls, and validation activities.
• Continued development of expertise in cGMP documentation and electronic document management systems.
• Opportunities for continued professional development and career growth within Afton Scientific.

Physical & Work Requirements

• Ability to stand for extended periods as necessary.
• Ability to lift up to 50 pounds and bend and reach as required.
• Near vision correctable to 20/20, including through corrective eyewear when necessary.
• Regular on-site attendance is required.