Manufacturing Documentation Specialist

Headquartered in Nashville, TN – one of the fastest-growing and most exciting cities in the United States – August Bioservices is a privately-owned, high-growth, and high-impact Contract Development Manufacturing Organization (CDMO). As a US-based outsourcing partner that provides a wide array of expert drug discovery, drug formulation, and drug manufacturing services to pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical industry.

Our work is instrumental in helping to develop molecules today that can become the life-changing therapies of tomorrow. To support our growth plans, August is investing significant capital in a two-phase expansion project – including building a new state-of-the-art facility adjacent to our current facility. For those seeking dynamic opportunities, rewarding career paths and a chance to make a difference in global health, come grow with August!

The Manufacturing Documentation Specialist supports GMP manufacturing by performing detailed review of batch production records and driving corrections. This role plays a critical part in ensuring accurate, compliant, and timely batch record review activities in support of batch disposition and release.

The Manufacturing Documentation Specialist collaborates closely with Manufacturing, Quality, and other cross-functional teams to ensure documentation accuracy, data integrity, and compliance with current Good Manufacturing Practices (cGMP) and applicable regulatory requirements. This position also supports record release, continuous improvement and inspection readiness activities within a fast-paced, regulated manufacturing environment.

• Review executed batch production records to support batch disposition and release activities.
• Identify and drive continuous improvements to GDP through record enhancements.
• Track GDP performance and record release timing through sitewide metrics.
• Participate in on the floor real-time review.
• Create, revise, proofread, format, and merge GMP documentation, including SOPs, batch records, and logbooks in support of site operations.
• Support Manufacturing on the Floor by assisting with documentation review, clarification of GMP requirements, and real-time support.
• Ensure adherence to company policies, procedures, and applicable regulatory requirements, including FDA, ICH, and global GMP standards.
• Support client audits and regulatory inspections by FDA and other regulatory agencies, including preparation and retrieval of documentation.
• Communicate effectively with cross-functional teams to resolve documentation issues and support timely completion of quality activities.

• Bachelor of Science degree in Life Sciences, or a related discipline required, or an equivalent combination of education and relevant experience.
• Minimum of two (2) to three (3) years of experience working in a regulated pharmaceutical, biotechnology, or medical device manufacturing environment required.
• Minimum of two (2) years of direct experience performing batch record review activities required.

• Working knowledge of cGMP requirements, including 21 CFR Parts 210, 211, 820, and familiarity with PIC/S Guide to Good Manufacturing Practice Parts I and II or EU GMP guidelines, including Annex 1.
• Knowledge of FDA Guidance on Aseptic Processing and 21 CFR Part 11 electronic records and signatures requirements preferred.
• Proficiency in electronic quality management systems, including Master Control or equivalent platforms.
• Strong attention to detail and documentation accuracy, with the ability to identify errors, inconsistencies, and compliance gaps.
• Excellent organizational and time management skills, with the ability to prioritize multiple tasks in a fast-paced environment.
• Strong written and verbal communication skills, with the ability to communicate clearly and professionally with cross-functional teams.
• Ability to work independently while maintaining accountability to quality standards, timelines, and procedures.
• Demonstrated commitment to data integrity, compliance, and continuous improvement.

The physical…