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August Bioservices

Associate Technology Transfer Engineer (MSAT)

Nashville, TN, United States

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Job details

Posting language: English
Posted: Aug 3, 2026

Original 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 Associate Technology Transfer Engineer is responsible for assigned tasks associated with the technology transfer for sterile drug products and Biologics. The responsibilities include working with Formulation Development, Process Engineers, Analytical Development, Production, Quality, and Regulatory to identify product and process criticalities and finding scientific data driven solutions to any Technology Transfer process. Associate Technology Transfer Engineers will generally lead maintenance of more established programs or support more experienced leads in designing and implementing more complex New Product Introductions.

Apart from supporting Technology Transfer activities, the position requires writing of technical documents to support, including protocols, reports, SOPs, Work Instruction, Batch records, and technical and risk assessments. The Engineer is this role is expected to work with other Technology technical services/process engineers to support process development within a team-based environment. This position will be responsible for participating in interdisciplinary teams and primary contact for the operations team throughout the product’s lifecycle. The Engineer is supported directly by more experienced Technology Transfer Engineers and departmental leadership as required.

ESSENTIAL DUTIES & RESPONSIBILITIES

Review of technology transfer documents such as product development reports, batch manufacturing and/or packaging records to provide the technical analysis for the overall process.
Based on analysis, identify gaps in capabilities needed to support new product/process introductions and recommend solutions to close these gaps
Support the evaluation of collected data during development and scale-up activities and recommend opportunities for process optimization for assigned projects
Work with leads or established SME’s training and familiarization efforts for new processes and equipment including development of operation SOP and work instructions for assigned projects
Support execution of Toxicological, Clinical, Scale up, Exhibit/Registration, Commercial manufacturing and process Performance Qualification/Validations with the production team inside production areas.
Support or lead the identification and procurement request process of materials recommended for assigned client projects
Maintain a clean, organized and documentation compliant R&D laboratory and pilot-scale spaces including proper storage and labeling of materials specific to client
Support the evaluation and selection of new equipment in support of fill/finish production operations in collaboration with client and internal stakeholders.
Participate in multidisciplinary project teams through the complete product transfer journey to support ongoing client projects on-time
Identify opportunities to recommend additional value-added services through sound technical evaluation of client product and processes
Support execution of phase specific studies based on DOE (Design of Experiments) as needed, for formulation optimization and process confirmation.
Apply elements of Quality-By-Design (QbD) approach in the product development program to improve the drug formulation and manufacturing process with support from more experienced team members or SME’s.
Contribute to Investigations and Corrective Actions analysis and support.
Write comprehensive technical reports, business evaluations, process description with supervision where required.
Support revisions to documents including master batch records, protocols and reports, SOPs, Work Instructions, and other necessary technical documents.
Support peer review and approval of protocols, batch records and summary reports
Troubleshoot and resolve less complex technical issues, diagnosing technical problems and identifying short and long-term solutions
Working with Cross-Functional Team leads to identifying opportunities for enhancements and champion projects which will improve overall site function.
Aptitude to learn and apply Quality system software such as Master control and related task such MOC (change control), CAPA, Issue Reviews, Work Orders, collaboration, and approval of various documents.

QUALIFICATIONS

• The candidate requires B.S in Pharmaceutical Sciences (or equivalent), M.S in Pharmaceutical Sciences (or equivalent), or PhD in Pharmaceutical Sciences (or equivalent).

• The candidate requires B.S in Pharmaceutical Sciences (or equivalent) with 1-2 year of experience, M.S in Pharmaceutical Sciences (or equivalent) with <1 year of experience, or PhD in Pharmaceutical Sciences (or equivalent) with <1 year of experience.

KNOWLEDGE, SKILLS, & ABILITIES

Knowledge of general pharmaceutical manufacturing unit operations.
Knowledge of general pharmaceutical processing technologies such as mixers, transfer pumps, temperature control devices
Knowledge of general process requirements for sterile operations including: compounding, sterile filtration, aseptic formulation, sterile filling for vials, pre-filled syringes and flexible IV bags
Software: Minitab® (or equivalent), Microsoft Office® etc., Microsoft Visio

PHYSICAL REQUIREMENTS

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Prolonged periods sitting at a desk and working on a computer.
Must be able to lift up to 25 pounds at times.

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.

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!

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More about this job

Skills

Packaging
Procurement
Documentation
Collaboration
Manufacturing processes
Troubleshoot
MasterControl
Pharmaceutical processes
Control systems
Minitab
Microsoft Office
Microsoft Visio
Heavy lifting

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