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Biotech Startup Jobs in Florida (NOW HIRING)

Who We Are Novir is an emerging diagnostic biotechnology company with an unmatched team of ... Physically traveling from one work site to another Novir is a fast-growing startup with a work hard ...

... and startup, load calculations, utility assessments, energy modeling, design reports, code ... Life Sciences (Pharmaceutical, Biotech, Laboratory) or Food & Beverage industry experience

... and startup, load calculations, utility assessments, energy modeling, design reports, code ... Life Sciences (Pharmaceutical, Biotech, Laboratory) or Food & Beverage industry experience

Who We Are Novir is an emerging diagnostic biotechnology company with an unmatched team of ... Physically traveling from one work site to another Novir is a fast-growing startup with a work hard ...

Customer Success Manager

Saint Petersburg, FL · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... high-growth or startup companies Proven track record of driving high customer retention ... life sciences, biotechnology, or laboratory supplies industry Experience with collections or ...

Customer Success Representative

Saint Petersburg, FL · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... high-growth or startup companies Proven track record of driving high customer retention ... biotechnology, or laboratory supplies industry Familiarity with customer health scoring models ...

Sales Manager

Saint Petersburg, FL · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... or startup environments Proven track record of consistently hitting or exceeding team revenue ... biotechnology, or laboratory supplies industry Adaptable and resilient, with experience leading ...

Showing results 21-38

Biotech Startup information

See Florida salary details

$18.7K

$75.7K

$176.4K

How much do biotech startup jobs pay per year?

As of Aug 13, 2026, the average yearly pay for biotech startup in Florida is $75,723.00, according to ZipRecruiter salary data. Most workers in this role earn between $39,829.00 and $92,405.00 per year, depending on experience, location, and employer.

What is a biotech startup?

A Biotech Startup job involves working in an early-stage company that develops innovative biological or medical technologies. Roles can vary widely, including research, product development, regulatory affairs, and business operations. Employees often wear multiple hats, contributing to both scientific advancements and business growth. The fast-paced environment requires adaptability, problem-solving skills, and a passion for innovation.

What are the key skills and qualifications needed to thrive in a biotech startup?

To thrive at a biotech startup, you need a strong background in life sciences or bioengineering, paired with an entrepreneurial mindset and practical research experience. Familiarity with laboratory equipment, data analysis software, and, in many cases, regulatory compliance certifications like GLP or GMP are vital. Exceptional adaptability, problem-solving abilities, and teamwork skills are also crucial in this fast-paced, multidisciplinary environment. These competencies help ensure innovation, rapid iteration, and successful navigation of the complex challenges faced by emerging biotech companies.

What are some unique challenges of working at a biotech startup compared to larger organizations?

Working at a biotech startup often means taking on a wide variety of responsibilities, as teams are usually small and roles can be less narrowly defined than at established companies. You may regularly transition between lab research, project management, and business development tasks, which can be both challenging and rewarding. Limited resources, tight deadlines, and the pressure to rapidly produce results are common, but these challenges also provide opportunities for accelerated learning and career advancement. Many employees find the collaborative, innovative atmosphere and the ability to make a tangible impact particularly fulfilling in this setting.

What are the most commonly searched types of Biotech Startup jobs in Florida?

The most popular types of Biotech Startup jobs in Florida are:

What are popular job titles related to Biotech Startup jobs in Florida?

For Biotech Startup jobs in Florida, the most frequently searched job titles are:

What cities in Florida are hiring for Biotech Startup jobs?

Cities in Florida with the most Biotech Startup job openings:

Infographic showing various Biotech Startup job openings in Florida as of August 2026, with employment types broken down into 93% Full Time, 4% Part Time, and 3% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $75,723 per year, or $36.4 per hour.

Senior Device Engineer, Pharmaceutical R&D

Transpire BIO Inc.

Weston, FL • On-site

$99K - $136K/yr

Full-time

Re-posted yesterday


Job description

Position Summary
The Senior Device Engineer is responsible for device engineering activities in the context of pharmaceutical research and development (R&D). The device mechanical engineer will be responsible for early to late-stage device development activities and commercialization of drug-device combination products. The Device engineer will be responsible for design, prototyping, technical analysis, and testing of orally inhaled and nasal drug products (OINDPs). Provide device engineering leadership in the direction, initiation, planning, coordination, implementation, execution, control, and completion of specific device project(s) ensuring consistency with organizational strategy, commitments, and goals. The device engineer will need to ensure that the device designs meet user needs, regulatory and quality requirements, and consider manufacturability. This is a hands-on position which requires daily tactical responsibilities leading up to strategic decisions.
Essential Duties and Responsibilities
  • In support of the Product Development Teams, provide technical leadership in the device development area.
  • Execute design and development of orally inhaled and nasal drug products (OINDPs) following design controls.
  • Lead and execute analysis for device and product characterization, design feasibility, and design verification.
  • Lead and execute technical analyses including statistical analysis and tolerance analysis.
  • Lead root cause investigations.
  • Support scale-up and commercialization efforts.
  • Document studies and author documents per US FDA, EMA, MHRA and other global health authority requirements.
  • Interface and lead activities with third party contract research, development, and manufacturing organizations.
  • Contribute towards and maintain device design history files (DHF).
  • Document standard operating procedures (SOPs) for design controls in the context of pharmaceutical drug-device combination products.
  • Provide project updates/reporting through program governance.
  • Provide leadership and support for inter-site best practices (technology transfer, process validation, etc.) and phase appropriate guidelines and policies.
  • Execute project strategy, priorities, and milestones ensuring visibility and accountability.
  • Proactively lead with integrity and engage cross functional project teams and stakeholders.
  • Support organizational / departmental initiatives.
  • Prepare and conduct presentations to all levels of the organization which may include project technical and budgetary information.

Required Qualifications
  • A M.S, in Mechanical Engineering, Electrical Engineering, Material Sciences or related discipline with 7 to 10 years, B.S. with 10 to 14 years device development experience in pharmaceutical or related field.
  • Experience with device development in the context of pharmaceutical R&D and product development is a must to have.
  • Must possess expert knowledge of mechanical design with preference for SolidWorks.
  • Must possess expert knowledge of tools to conduct statistical and tolerance analysis.
  • Must possess knowledge of manufacturing processes including injection molding and metal machining processes.
  • Must possess knowledge of regulations and standards including US 21 CFR Part 820, ISO 13485, ISO 14971, ISO 10993, EU MDR etc.
  • Experience with device assembly processes including manual, semi-automated and/or commercial scale automated processes is a plus.
  • Experience in development of orally inhaled and nasal drug products (OINDPs) is a plus.
  • Experience in mold tool design, optimization and qualification is a plus to have.
  • Experience with Notified Bodies and CE marking is a plus.
  • Strong English language skills including writing ability and oral communication.
  • Demonstrates good judgment as well as cultural, social, and environmental awareness.

Preferred Qualifications
  • Experience in a regulated laboratory (pharma, biotech, medical device, mechanical, or environmental)
  • Knowledge of GMP, GLP, or ISO standards

Why Join Us?
We are a fast-growing pharmaceutical startup dedicated to innovation and improving patient outcomes. Join us to gain hands-on experience in a growing pharmaceutical business, get exposure to various functions with opportunities for career development and work in a collaborative and supportive work environment.