Manufacturing Documentation Specialist

August Bioservices; Nashville (TN); On-site; USD 65,000 - 95,000; Full time

Job summary

August Bioservices in Nashville, TN, is seeking a Manufacturing Documentation Specialist to ensure accurate, compliant batch record review and documentation control in a fast-paced GMP environment. You will collaborate with Manufacturing, Quality, and cross-functional teams to support batch disposition, FDA inspections, and continual improvement while maintaining data integrity.

The role requires a Life Sciences degree and 2–3 years in regulated pharma manufacturing with direct batch record

Qualifications

• Bachelor of Science degree in Life Sciences or related field.
• 2–3 years of experience in a regulated pharma/biotech manufacturing environment.
• Minimum 2 years direct experience performing batch record review.

Responsibilities

• Review executed batch production records to support 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.
• Support Manufacturing on the Floor by assisting with documentation review and GMP requirements.
• Ensure adherence to FDA, ICH, and global GMP standards.
• Support client audits and regulatory inspections by FDA and others, including documentation retrieval.
• Communicate effectively with cross-functional teams to resolve documentation issues.

Skills

GMP knowledge

cGMP compliance

Documentation control

Batch record review

FDA/ICH familiarity

MasterControl

Education

Bachelor of Science in Life Sciences

Equivalent combination of education and experience

Tools

MasterControl

Job description

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.

ESSENTIAL DUTIES & RESPONSIBILITIES

• 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.

QUALIFICATIONS

• 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.

KNOWLEDGE, SKILLS, & ABILITIES

• 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 MasterControl 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.

PHYSICAL REQUIREMENTS

• Ability to perform all required gowning.
• Ability to work in an office and manufacturing environment, including time spent on the production floor as needed.
• Ability to sit or stand for extended periods while reviewing documentation and working at a computer.
• Ability to use standard office equipment, including computers, printers, and scanners.
• Ability to lift and carry materials or files up to 20 pounds, with or without reasonable accommodation.
• Ability to wear required personal protective equipment (PPE) when supporting activities in manufacturing areas.

At August Bioservices, Our Credo is our culture. Everything we do, we do with great care. We believe in the promise of discovery and the power of science to transform lives. We assert that excellence is not a static destination, but a standard, and an every-day measuring stick of our advancement. We aspire to unlock the potential in every person, every process and every molecule – from start to finish. We are committed to doing the right thing the first time and every time, meeting or exceeding all regulatory requirements. We strive to be exceptional, preferred and indispensable partners for our customers; responsible and engaged citizens within our communities; and active, mindful stewards of our environment.

We are August Bioservices. We are pointing the way forward. If this sounds like your kind of working environment, we want you on our team!

August Bioservices is an equal opportunity employer and values diversity. All aspects of employment including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs. August Bioservices does not discriminate on the basis of any status protected under federal, state, or local law.