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!

· Lead the preparation, review, and approval of analytical reports, data summaries, protocols, specifications, analytical methods, and other technical documentation.

· Review analytical data packages supporting release testing and stability studies, including raw chromatographic data and Empower-generated reports.

· Collaborate closely with Scientists and cross-functional teams to ensure analytical documentation and reports are completed accurately and within established timelines.

· Support analytical method development, validation, qualification, transfer, and lifecycle management activities across development and commercial programs.

· Prepare, review, and manage technical documents, including analytical methods, validation protocols and reports, specifications, and analytical trend reports.

· Coordinate analytical reporting activities for drug substance and drug product stability programs, ensuring analytical data are accurately documented, assessed, and communicated.

· Participate in investigations associated with deviations, OOS, OOT, and other laboratory events, ensuring appropriate documentation and compliance with quality and regulatory requirements.

· Lead continuous improvement initiatives designed to enhance analytical reporting processes, data integrity, document quality, and operational efficiency.

· Master's degree with 2+ years of pharmaceutical experience or a Bachelor's degree with 3-5 years of pharmaceutical experience.

· Must have 3 or more years of reviewing cGMP analytical method documents.

· Experience in analytical development, analytical reporting, or related pharmaceutical development functions.

· Strong understanding of small-molecule analytical development, method validation and transfer, stability testing, specifications, and analytical control strategies.

· Demonstrated experience preparing, reviewing, and approving technical documentation, including analytical methods, protocols, and reports.

· Working knowledge of analytical techniques such as HPLC/UPLC, LC-MS, GC-MS, ICP-MS, wet chemistry, particle size analysis, capillary electrophoresis, and other pharmaceutical characterization techniques.

· Familiarity with ICH, FDA, EMA, and other global regulatory requirements applicable to analytical development.

· Strong scientific writing, data interpretation, problem-solving, and project management capabilities.

· Excellent written and verbal communication skills, with the ability to clearly convey complex technical information to diverse audiences.

· Proficiency in Microsoft Office applications

· Proven ability to collaborate effectively within cross-functional, matrixed organizations and establish strong relationships with internal stakeholders and external partners.

· Highly organized and capable of managing multiple priorities and deadlines in a fast-paced biotech environment.

· Able to work in flexible shifts or weekends to meet timelines.