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Biotech Equity Research Associate Jobs in Tennessee

Tom James Company

Payroll Associate

Franklin, TN

$20 - $22/hr

Review and validate payroll changes, including pay rates, bonuses, allowances, equity/stock ... research, and correction of coding issues * Assist with payroll cash account balancing and related ...

Tom James Company

Payroll Associate

Franklin, TN · On-site

$20 - $22/hr

Review and validate payroll changes, including pay rates, bonuses, allowances, equity/stock ... research, and correction of coding issues * Assist with payroll cash account balancing and related ...

Tom James Company

Payroll Associate

Franklin, TN · On-site

$20 - $22/hr

Review and validate payroll changes, including pay rates, bonuses, allowances, equity/stock ... research, and correction of coding issues * Assist with payroll cash account balancing and related ...

Spectra Tech, Inc.

Fermentation Manager

Memphis, TN · On-site

Partner with R&D for product scale-up and Quality Assurance (QA) for final product approval ... Science, Microbiology, Biotechnology, Chemical Engineering, or a related field. Experience ...

New

SPECTRA TECH INC

Fermentation Manager

Memphis, TN

Partner with R&D for product scale-up and Quality Assurance (QA) for final product approval ... Science, Microbiology, Biotechnology, Chemical Engineering, or a related field. Experience ...

New

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Biotech Equity Research Associate information

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$14

$29

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How much do biotech equity research associate jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for biotech equity research associate in Tennessee is $29.53, according to ZipRecruiter salary data. Most workers in this role earn between $23.80 and $33.61 per hour, depending on experience, location, and employer.

What is a biotech equity research associate?

Biotech Equity Research Associates are professionals who analyze biotechnology companies and the broader biotech sector to provide investment insights and recommendations to clients, such as institutional investors or portfolio managers. They support senior analysts in evaluating clinical trial data, financial statements, and industry trends to assess the potential of biotech firms. Their work involves building financial models, preparing research reports, and sometimes interacting with company management. The goal is to help investors make informed decisions about buying, holding, or selling biotech stocks.

What are the key skills and qualifications needed to thrive as a biotech equity research associate?

To thrive as a Biotech Equity Research Associate, you need a strong background in finance and life sciences, typically supported by a degree in biology, chemistry, finance, or a related field. Familiarity with financial modeling, Bloomberg Terminal, and Excel, as well as certifications like CFA, are often required. Analytical thinking, attention to detail, and excellent communication skills help you stand out when interpreting data and presenting investment recommendations. These skills and qualities are crucial for generating insightful research, supporting investment decisions, and effectively communicating complex scientific and financial information to stakeholders.

What are some common challenges faced by biotech equity research associates when analyzing early-stage companies?

One frequent challenge for Biotech Equity Research Associates is evaluating early-stage companies that often lack extensive financial histories or approved products. This requires associates to rely heavily on scientific data, clinical trial progress, and management credibility to assess future growth potential. Navigating the technical complexity of drug development pipelines and regulatory uncertainties also demands strong analytical skills and ongoing collaboration with scientific experts. Staying updated on industry trends and regulatory changes is essential to provide accurate and insightful recommendations.

What is the difference between Biotech Equity Research Associate vs Biotech Analyst?

AspectBiotech Equity Research AssociateBiotech Analyst
CredentialsBachelor's degree in life sciences, finance, or related field; often pursuing CFA or similar certificationsBachelor's or master's in biology, biotech, or finance; CFA preferred
Work EnvironmentFinancial firms, investment banks, or asset management companiesFinancial institutions, research firms, or investment firms
Industry UsageSupports investment decisions by analyzing biotech companiesProvides detailed industry and company analysis for investment purposes

Both roles involve analyzing biotech companies, but the Biotech Equity Research Associate typically supports senior analysts with data collection and report preparation, while the Biotech Analyst conducts in-depth research and makes investment recommendations. The associate role is often an entry point, focusing on data and support tasks, whereas the analyst role involves more independent analysis and decision-making.

What are the most commonly searched types of Biotech Equity Research jobs in Tennessee?

The most popular types of Biotech Equity Research jobs in Tennessee are:

What are popular job titles related to Biotech Equity Research Associate jobs in Tennessee?

For Biotech Equity Research Associate jobs in Tennessee, the most frequently searched job titles are:

What job categories do people searching Biotech Equity Research Associate jobs in Tennessee look for?

The top searched job categories for Biotech Equity Research Associate jobs in Tennessee are:

What cities in Tennessee are hiring for Biotech Equity Research Associate jobs?

Cities in Tennessee with the most Biotech Equity Research Associate job openings:

Biotech Equity Research Associate jobs near you
Infographic showing various Biotech Equity Research Associate job openings in Tennessee as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $61,432 per year, or $29.5 per hour.

Associate Technology Transfer Engineer (MSAT)

Nashville, TN • On-site

August Bioservices
Pharmaceutical and Medicine Manufacturing • 51 - 200 employees
Learn more about August Bioservicesexternal

Full-time

Posted 27 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 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!

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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