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Biotechnology Engineer Jobs in Miami, FL (NOW HIRING)

STARLIMS

Technical Support Engineer

Hollywood, FL · On-site

... biotech, life sciences, food & beverage, manufacturing, petrochemical refineries and oil & gas ... The Technical Support Engineer delivers accurate and timely technical support, guidance, and ...

STARLIMS

Senior Software Engineer IV

Hollywood, FL · On-site +1

$112K - $147K/yr

Senior Software Engineer IV - STARLIMS Remote, U.S.| Full Time | R&D STARLIMS provides leading ... biotech, life sciences, food & beverage, manufacturing, petrochemical refineries and oil & gas ...

Danaher

Senior Mechanical Engineer

Miami, FL · On-site

$100 - $120K/hr

... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... The Senior Mechanical Engineer is responsible for projects related to new cost savings ...

CRB

Project Manager - Design

Miami, FL · On-site +1

Bachelor's or Master's degree in Architecture, Engineering, or related field. * 7+ years of experience in design project management, preferably in pharmaceutical or biotech facility design. * Strong ...

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All JobsBiotechnology Engineer JobsBiotechnology Engineer Jobs in Miami, FL

Biotechnology Engineer information

See Miami, FL salary details

$32.6K

$84K

$150.5K

How much do biotechnology engineer jobs pay per year?

As of Aug 29, 2026, the average yearly pay for biotechnology engineer in Miami, FL is $84,024.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,020.00 and $95,490.00 per year, depending on experience, location, and employer.

What does a biotechnology engineer do?

A Biotechnology Engineer applies principles of biology, chemistry, and engineering to develop products and technologies that improve human health, agriculture, and the environment. Their work includes designing processes for producing medicines, biofuels, and food, as well as developing equipment and systems for biotechnology applications. Biotechnology Engineers often collaborate with scientists and other engineers to innovate and solve complex biological problems, making their role crucial in advancing medical and agricultural technologies.

What are the key skills and qualifications needed to thrive as a biotechnology engineer?

To thrive as a Biotechnology Engineer, you need a strong background in biology, chemistry, and engineering principles, typically supported by a bachelor's or master's degree in biotechnology or a related field. Familiarity with laboratory equipment, bioinformatics tools, and regulatory standards such as GMP is essential. Critical thinking, problem-solving, and effective teamwork are standout soft skills in this role. These skills and qualities are crucial for developing innovative solutions and ensuring compliance in the rapidly evolving biotechnology industry.

What are some common challenges biotechnology engineers face when working on interdisciplinary teams?

Biotechnology Engineers often collaborate with professionals from biology, chemistry, computer science, and engineering backgrounds. A common challenge is bridging communication gaps due to varying technical vocabularies and priorities among disciplines. Successful engineers develop strong teamwork and communication skills to align goals, understand constraints, and integrate diverse expertise into innovative solutions. Building mutual respect and fostering open dialogue are essential for effective interdisciplinary collaboration.

What is the difference between Biotechnology Engineer vs Biomedical Engineer?

AspectBiotechnology EngineerBiomedical Engineer
Required CredentialsBachelor's or Master's in Biotechnology, Bioengineering, or related fieldsBachelor's or Master's in Biomedical Engineering, Bioengineering, or related fields
Work EnvironmentLaboratories, biotech companies, research facilitiesHospitals, medical device companies, research labs
Industry UsageBiotech firms, pharmaceutical companies, agricultural biotech
Common Search IntentComparing roles in biotech development and research

Biotechnology Engineers focus on developing and improving biotechnological products, often working in labs and biotech firms. Biomedical Engineers design medical devices and work closely with healthcare providers. While both roles require similar educational backgrounds, their work environments and industry applications differ, catering to different aspects of the life sciences sector.

Do biotechnology engineers make a lot of money?

Biotechnology engineers typically earn competitive salaries that vary based on experience, education, and location. According to industry data, the median annual wage is above the national average for engineering roles, with higher earnings possible for those with advanced skills or managerial responsibilities.

What are popular job titles related to Biotechnology Engineer jobs in Miami, FL?

For Biotechnology Engineer jobs in Miami, FL, the most frequently searched job titles are:

What job categories do people searching Biotechnology Engineer jobs in Miami, FL look for?

The top searched job categories for Biotechnology Engineer jobs in Miami, FL are:

Biotechnology Engineer jobs near you
Infographic showing various Biotechnology Engineer job openings in Miami, FL as of August 2026, with employment types broken down into 95% Full Time, 2% Part Time, and 3% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $84,024 per year, or $40.4 per hour.

Bioprocess Specialist, Upstream

Plantation, FL • On-site

Goodwin Biotechnology Inc
See more jobs at Goodwin Biotechnology Incexternal

Full-time

Re-posted 4 days ago

Job description

Description:

Scope of Function:

The Bioprocess Specialist position reports to the Upstream Manufacturing, Manager. Prior experience in GMP manufacturing, operation of GMP process equipment and aseptic technique are prerequisites. This role is responsible for supporting the overall Upstream GMP process, through the application of broad knowledge of theories and principles utilized to solve operational, as well as routine tasks in the production of bulk biologics from microbial and cell culture systems for Phase 1/11/111 and commercial GMP manufacturing.


Specific Duties:

• Operates pharmaceutical manufacturing equipment such as: incubators, wave reactors, single-use and stainless-steel bioreactors, single use mixers, depth filtration skids, TFF skids, chromatography skids and in process testing equipment.

• Executes all Upstream Clinical Manufacturing and Development operations, including but not limited to work functions in cell culture, cell banking, media optimization, seed train preparation, bioreactor operations, harvest/clarification, and technology transfer to manufacturing.

• Demonstrates, understands, and adheres to Goodwin Biotechnology policies, GMP standards and safety procedures.

• Performs and monitors critical processes, execute manufacturing batch records (MBR) for specific projects to manufacture cell-derived biopharmaceuticals in compliance with cGMP guidelines and regulation.

• Performs and monitors critical processes, execute manufacturing batch records (MBR) for specific projects to manufacture cell-derived biopharmaceuticals in compliance with cGMP guidelines and regulations.

• Supports the development of batch records, SOP’s and protocols as required.

• Supports other manufacturing processes teams and other GBI groups as necessary to achieve manufacturing goals.


This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change or new ones may be assigned at any time with or without notice.

Requirements:

Education and Experience Required:

• BS degree in Science or Engineering.

• Associate degree in science or engineering, or related field and minimum of 3 years of experience with biologic production processes under GMP compliance. Downstream experience preferred.

• Minimum of High School Diploma or equivalent and 3 years of experience with biologic production processes under GMP compliance. Upstream experience preferred.

• Excellent documentation skills including comprehension and review & establishing batch production records.