QA Documentation Specialist

Union Agener; Augusta (GA); On-site; USD 45,000 - 65,000; Full time

Benefits offered by this job

Competitive Benefits Package

Employee Assistance Program

401(k) Plan + Company Match

Vacation + End of Year Vacation

Growth Opportunities

Job summary

Union Agener in Augusta, GA is seeking a detail-oriented Quality Control/Quality Assurance professional to support manufacturing documentation and archival processes. You will print and issue batch records, manage document requests, act as documentation steward, perform document release and distribution, and maintain training modules related to SOPs and documentation activities.

A background in cGMPs and manufacturing plant operations is preferred.

Qualifications

• Minimum of a High School Diploma or GED.
• Preferred Associate's degree in a technical related field.
• Three (3) years of experience in Quality Control or Quality Assurance.
• Demonstrated knowledge/application of cGMPs and other pharmaceutical guidelines.

Responsibilities

• Print and issue batch records and labels for all manufacturing operations.
• Execute Document Requests to Create, Revise, Cancel, or Print.
• Act as a documentation steward (ensures a coordinated review of all associated documents).
• Perform document release (ensures a coordinated release of all associated documents).
• Perform document distribution (controlled copy), communication (email), and archive.
• Act as archive room manager.
• Support Training Module Management (courseware requests, roster inquiries, processing course credits, test answer keys).
• Maintain training modules and SOPs related to documentation activities.
• Spreadsheet and database maintenance.

Skills

Detail oriented

Results oriented

Strong interpersonal skills

Teamwork

Adapt to change

Education

High School Diploma or GED

Associate's degree (preferred)

Tools

SAP

Job description

Union Agener in Augusta, GA is seeking a detail-oriented Quality Control/Quality Assurance professional to support manufacturing documentation and archival processes. You will print and issue batch records, manage document requests, act as documentation steward, perform document release and distribution, and maintain training modules related to SOPs and documentation activities.

A background in cGMPs and manufacturing plant operations is preferred.