Biotech & Pharma STEM OPT Jobs in Tennessee
Tennessee's biotech and pharma sector, anchored by companies like Pfizer, Vanderbilt-affiliated research institutions, and a growing Nashville health-tech corridor, actively hires F-1 STEM OPT candidates for research, manufacturing, and regulatory roles. Memphis and Nashville lead in sponsorship activity, giving OPT holders strong options across the state.
Find Biotech & Pharma JobsOverview
Showing 5 of 13+ Biotech & Pharma STEM OPT Jobs in Tennessee










See all Biotech & Pharma STEM OPT Jobs in Tennessee
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Biotech & Pharma STEM OPT Jobs in Tennessee.
Get Access To All Jobs
Job Summary:
The Associate Scientist, R&D - Biological Sciences supports research and development activities by planning and executing laboratory experiments, maintaining accurate scientific documentation, analyzing results, and collaborating with cross-functional teams to advance product development and innovation. This role contributes to research projects from concept through commercialization and supports continuous improvement initiatives across assigned scientific disciplines. Assignments may include work in formulation sciences, biological sciences, analytical sciences, microbiology, or other R&D functions depending on business needs.
Key Responsibilities:
- Conduct laboratory experiments following established protocols and scientific methodologies.
- Design, execute, and document routine research studies under the guidance of senior scientists and project leaders.
- Analyze experimental data and communicate findings through written reports and presentations.
- Maintain accurate, organized, and compliant laboratory notebooks and technical documentation.
- Support new product development, product optimization, technology transfer, and continuous improvement initiatives.
- Operate, maintain, and troubleshoot laboratory equipment within assigned area of expertise.
- Prepare laboratory materials, reagents, samples, and test articles as required.
- Monitor, maintain, and organize laboratory inventory, supplies, and equipment.
- Collaborate with cross-functional teams including Research & Development, Manufacturing, Quality, Regulatory, and Operations to support project objectives.
- Follow all laboratory safety procedures, quality standards, and applicable Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), or other regulatory requirements as applicable.
- Manage multiple projects and priorities while meeting established timelines.
- Stay current with scientific literature, emerging technologies, and industry best practices.
- Perform other duties as assigned.
Required Qualifications:
- Bachelor's or Master's degree in Chemistry, Biology, Biochemistry, Biomedical Sciences, Chemical Engineering, or another related scientific discipline.
- 1–3 years of laboratory or research experience in an academic or industry setting.
- Experience conducting laboratory experiments and maintaining detailed scientific documentation.
- Strong analytical, organizational, and problem-solving skills.
- Excellent verbal and written communication skills.
- Ability to manage multiple priorities in a fast-paced environment.
- Proficiency with Microsoft Office applications.
Preferred Qualifications:
- Formulation development
- Cell biology
- Molecular biology
- Microbiology
- Analytical chemistry
- Product stability testing
- Product development and commercialization
- Laboratory instrumentation and analytical equipment
- cGMP, GLP, or FDA-regulated environments
Knowledge, Skills & Abilities:
- Scientific curiosity and strong attention to detail.
- Ability to learn new laboratory techniques and technologies.
- Strong troubleshooting and critical thinking skills.
- Ability to work independently while collaborating effectively within a multidisciplinary team.
- Excellent documentation and data integrity practices.
- Strong organizational and time management skills.
- Ability to communicate technical information to both scientific and non-scientific audiences.
Working Conditions:
- Laboratory environment with routine exposure to chemicals, biological materials, laboratory equipment, and personal protective equipment (PPE).
- Ability to stand for extended periods and occasionally lift up to 25 pounds.
- May require occasional travel between facilities or to support business needs.
Company Summary:
Crown is a proud member of the Revance Portfolio of skincare offerings. Revance is a global company developing, producing, and distributing industry-leading, differentiated products across aesthetics, skincare, and therapeutics. Revance drives innovation beyond convention to offer treatment options for individuals across generations. The Company's vision is to redefine excellence in aesthetics, skincare, and therapeutics through science-powered innovation, with an unwavering commitment to its providers, patients, and consumers. Revance's award-winning products are the result of robust research and development, a cornerstone for the Company, driven by renowned scientists.
What Revance invests in you:
- Competitive Compensation including base salary and annual performance bonus.
- Flexible PTO, holidays, and parental leave.
- Generous healthcare benefits, HSA match, 401k match, employer paid life and disability insurance, pet insurance, wellness discounts and much more!
This section of the job description is required by the American with Disability Act (ADA). The ADA requires that job descriptions reflect the physical and mental demands required to effectively perform the essential duties of the job. The ADA prohibits employers from discriminating against a "qualified individual with a disability" in all aspects of the employment relationship. A "qualified individual with a disability" is "an individual who meets the education, experience, skill, and other job-related requirements of a position held or desired, and who, with reasonable accommodation, can perform the essential functions of a specified job."
Revance is an Equal Opportunity employer. All qualified applicants will receive consideration for employment based on merit, without regard to race, color, religion, sex, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.
STEM OPT Biotech & Pharma Job Roles in Tennessee
See all Biotech & Pharma STEM OPT Jobs in Tennessee
Sign up for free to filter by visa type, set job alerts, and find employers with verified sponsorship history.
Search Biotech & Pharma Jobs in TennesseeBiotech & Pharma STEM OPT Sponsorship Jobs in Tennessee: Frequently Asked Questions
Which biotech & pharma companies sponsor F-1 STEM OPT visas in Tennessee?
Tennessee employers with a record of F-1 STEM OPT sponsorship in biotech and pharma include Pfizer's Memphis operations, Genoptix, and research-adjacent employers tied to Vanderbilt University Medical Center and the University of Tennessee Health Science Center. Contract research organizations operating in Nashville and pharmaceutical manufacturers in the greater Memphis area also appear in DOL Labor Condition Application filings for STEM OPT roles.
Which cities in Tennessee have the most biotech & pharma F-1 STEM OPT sponsorship jobs?
Nashville concentrates the highest volume of biotech and pharma STEM OPT sponsorship activity, driven by its health-tech cluster and proximity to Vanderbilt's research ecosystem. Memphis is the secondary hub, with pharmaceutical manufacturing and distribution employers filing LCAs for STEM-designated roles. Knoxville, home to Oak Ridge National Laboratory's affiliated private sector partners, also generates STEM OPT opportunities in life sciences and research.
How do I find biotech & pharma F-1 STEM OPT sponsorship jobs in Tennessee?
Migrate Mate filters biotech and pharma job listings specifically for F-1 STEM OPT eligibility, surfacing Tennessee employers with verified sponsorship history based on DOL filing data. This saves significant time compared to manually reviewing LCA disclosures. Search by city, Nashville, Memphis, or Knoxville, and filter by role type such as research associate, regulatory affairs specialist, or quality control analyst to narrow results to positions that match your OPT authorization window.
What types of biotech & pharma roles typically qualify for F-1 STEM OPT sponsorship in Tennessee?
Roles that qualify must correspond to a STEM-designated Classification of Instructional Programs code tied to your degree. In Tennessee's biotech and pharma sector, qualifying positions commonly include bioinformatics analyst, clinical research associate, process development scientist, regulatory affairs specialist, quality assurance engineer, and pharmaceutical manufacturing technologist with a relevant engineering or chemistry degree. The specific CIP code match between your degree and the job's SOC classification determines eligibility, not the job title alone.
Are there state-specific considerations for F-1 STEM OPT sponsorship in Tennessee's biotech sector?
Tennessee does not impose state-level visa sponsorship requirements, but employers in regulated biotech and pharma environments must meet federal E-Verify enrollment requirements for all STEM OPT hires, this is a federal condition, not Tennessee-specific. Tennessee's comparatively lower cost of operating a lab or manufacturing facility has attracted pharmaceutical contract manufacturers to the state, which can translate to more entry-level STEM OPT openings than in higher-cost biotech hubs. Always confirm an employer's E-Verify status before accepting an offer.