Document Control Specialist, QA & eQMS MasterControl

August Bioservices; Nashville (TN); On-site; USD 48,000 - 64,000; Full time

Job summary

August Bioservices, headquartered in Nashville, TN, is seeking a Document Control Specialist to support Quality Assurance documentation systems. You will manage electronic and physical documents, create and revise GMP records, and coordinate with cross‑functional teams to ensure compliant documentation practices across the site.

The role emphasizes accuracy, attention to detail, and the ability to work independently in a fast-paced environment.

Qualifications

• Bachelor of Science in a Life Sciences, Quality, or related field.
• 0–3 years of document management experience within a pharmaceutical FDA-regulated environment.

Responsibilities

• Implement, administer, and improve the Document Control and Archiving Function within Quality Assurance.
• Create/revise SOPs, batch records, and GMP documents in support of site operations in eQMS.
• Proofread, merge, and format documents as they progress through eQMS.
• Initiate document reviews in eQMS and manage logbooks.
• Support site audits/inspections and assist cross‑functional teams with document routing.

Skills

Document management

Quality systems

SOPs

GMP

Education

B.S./B.Sc in Life Sciences or Quality

Job description

August Bioservices, headquartered in Nashville, TN, is seeking a Document Control Specialist to support Quality Assurance documentation systems. You will manage electronic and physical documents, create and revise GMP records, and coordinate with cross‑functional teams to ensure compliant documentation practices across the site.

The role emphasizes accuracy, attention to detail, and the ability to work independently in a fast-paced environment.