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Drug Discovery Development Jobs in Tennessee (NOW HIRING)

August Bioservices

Quality Engineer

Nashville, TN · On-site

$69K - $89K/yr

... 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 ...

August Bioservices

Critical Utilities Technician

Nashville, TN · On-site

$19.25 - $26.25/hr

... 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 ...

August Bioservices

Critical Utilities Technician

Nashville, TN · On-site

$19.25 - $26.25/hr

... 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 ...

August Bioservices

GMP Cleaner - 3rd Shift

Nashville, TN · On-site

... 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 ...

August Bioservices

Critical Utilities Technician

Nashville, TN · On-site

$19.25 - $26.25/hr

... 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 ...

August Bioservices

GMP Cleaner - 3rd Shift

Nashville, TN · On-site

... 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 ...

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Drug Discovery Development information

What is drug discovery and development?

Drug discovery and development is the process of identifying new candidate medications and bringing them to market. It involves several stages, including target identification, screening of compounds, preclinical studies, clinical trials, and regulatory approval. The goal is to find safe and effective drugs that can treat or prevent diseases. This process is complex, time-consuming, and requires collaboration among scientists, clinicians, and regulatory agencies. Successful drug development can take many years and significant financial investment.

What are some common challenges faced by professionals in drug discovery development when transitioning from early-stage research to clinical trials?

One common challenge in Drug Discovery Development is ensuring that promising compounds identified during early-stage research demonstrate both efficacy and safety in preclinical and clinical settings. This transition requires close collaboration between multidisciplinary teams, including chemists, biologists, toxicologists, and regulatory experts. Navigating regulatory requirements, securing funding, and managing timelines are also significant challenges. Professionals must be adept at adapting project strategies based on new data and feedback from regulatory agencies to keep development on track.

What are the key skills and qualifications needed to thrive in drug discovery development, and why are they important?

To thrive in Drug Discovery Development, you need a solid background in biochemistry, pharmacology, or related life sciences, typically with an advanced degree such as a PhD or MS. Proficiency in laboratory techniques, data analysis software (e.g., Prism, ChemDraw), and familiarity with regulatory standards are essential. Strong problem-solving skills, attention to detail, and effective teamwork set outstanding professionals apart in this field. These skills and qualities are critical for efficiently developing safe, effective drugs and successfully advancing compounds through the discovery pipeline.

What is the difference between Drug Discovery Development vs Drug Regulatory Affairs?

AspectDrug Discovery DevelopmentDrug Regulatory Affairs
Primary FocusIdentifying and developing new drug candidates through research and laboratory workEnsuring compliance with regulations and obtaining approvals for drugs
Work EnvironmentLaboratories, research facilities, early-stage development teamsRegulatory agencies, pharmaceutical companies, compliance departments
Required CredentialsDegree in life sciences, chemistry, or related fields; often PhDs or advanced degreesDegree in life sciences, pharmacy, or related fields; regulatory certifications beneficial

Drug Discovery Development focuses on creating new drugs through research, while Drug Regulatory Affairs ensures these drugs meet legal standards for market approval. Both roles are essential in the pharmaceutical industry but differ in their core responsibilities and work environments.

What are popular job titles related to Drug Discovery Development jobs in Tennessee?

For Drug Discovery Development jobs in Tennessee, the most frequently searched job titles are:

What job categories do people searching Drug Discovery Development jobs in Tennessee look for?

The top searched job categories for Drug Discovery Development jobs in Tennessee are:

What cities in Tennessee are hiring for Drug Discovery Development jobs?

Cities in Tennessee with the most Drug Discovery Development job openings:

Drug Discovery Development jobs near you
Infographic showing various Drug Discovery Development job openings in Tennessee as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, 2% Contract, and 1% Nights. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution.

Quality Engineer

August Bioservices

Nashville, TN • On-site

$69K - $89K/yr

Full-time

Re-posted 21 days ago

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 Quality Engineer is responsible for supporting incoming new client projects from the Quality perspective at August Bioservices. Successful candidates will be a team player and have exceptional technical and communication skills, a strong background in Quality, and a high ability to collaborate with various levels of the organization.
Responsibilities
  • The Quality Assurance Engineer represents the Quality function in internal and external meetings related to new client projects, determining deliverables and timelines, and communicating upcoming activities with all of the Quality Organization (Quality Assurance, Quality Control and Validation).
  • Support technology transfer of product and processes from clients into August Bioservices manufacturing and laboratories from the Quality perspective. Project may span R&D, Formulation Development, Clinical, and Commercial Manufacturing.
  • Works cross functionally with various internal departments to effectively transfer and maintain processes in the facility.
  • Help proactively identify CMC critical path items, risks, and impediments to successful transfer, and drive the identification and development of solutions to help mitigate these risks.
  • Provide support on projects to streamline new product introduction, provide feedback in Change Review Board for change controls to introduce new products.
  • Develop and implement phase appropriate strategies for efficient transfers and identification of Quality deliverables.
  • Works with Product Quality Assurance and Manufacturing to support generation of appropriate batch documentation.
  • Communicates project status, upcoming deliverables and timeliness to the Quality Organization.
  • This position will work in a cross-functional group with Manufacturing, Engineering, Supply Chain, and Commercial Operations to drive technical transfer of client products into August Bioservices for manufacture and laboratory testing.
  • This position will be client facing and the candidate should possess the ability to work collaboratively with clients and internal cross-functional stakeholders to move projects forward.
  • Provides support during internal audits and regulatory inspections.
  • Adhere to company policies and applicable regulatory agencies requirements (ICH, FDA etc.) to ensure compliance.
  • Communicate clearly with cross-functional teams.

Requirements
  • Bachelor's or Master's Degree and 5+ years of experience in Quality Assurance within a biotechnology, biologics, or pharmaceutical manufacturing facility.
  • Must have proven track record with CMC and technology transfer.
  • GMP compliance knowledge including knowledge of 21CFR210, 211, 820 and the PICS Guide to Good Manufacturing Practices Part 1 and 2 or the EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use, including Annex 1 and FDA Guidance on Aseptic Processing and Part 11 compliance knowledge preferred.
  • Work occurs in a fast-paced environment. Individual must be able to efficiently prioritize own work and quickly communicate project information to the team.

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 15 pounds at times.

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.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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