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Biotech Process Engineer Jobs in Florida (NOW HIRING)

Manufacturing Engineer

Orlando, FL · On-site

$68K - $87K/yr

... biotechnology, medical device, or regulated manufacturing environments. * Basic understanding of manufacturing processes and engineering principles. * Familiarity with GMP/cGMP, FDA regulations, ISO ...

... and biotechnology? At Pall Corporation, one of Danaher's 15+ operating companies, our work saves ... Analyze process performance and partner with Quality and EHS teams to ensure compliance with ...

... and biotechnology? At Pall Corporation, one of Danaher's 15+ operating companies, our work saves ... Analyze process performance and partner with Quality and EHS teams to ensure compliance with ...

Our client is a leading biotechnology company that combines technological expertise with world ... Interface with Manufacturing, Packaging, Engineering, MSAT, PD, and QA/QC teams to resolve process ...

Senior Manufacturing Engineer

Pensacola, FL · On-site

$86K - $117K/yr

... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... Solve process and equipment problems, document causes, and implement solutions to prevent ...

Senior Manufacturing Engineer

Pensacola, FL · On-site

$86K - $117K/yr

... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... Solve process and equipment problems, document causes, and implement solutions to prevent ...

... and biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives--and ... Solve process and equipment problems, document causes, and implement solutions to prevent ...

Senior Manufacturing Engineer

Pensacola, FL · On-site

$86K - $117K/yr

... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... Solve process and equipment problems, document causes, and implement solutions to prevent ...

Senior Manufacturing Engineer

Pensacola, FL · On-site

$86K - $117K/yr

... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... Solve process and equipment problems, document causes, and implement solutions to prevent ...

... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... Support Environment, Health, and Safety (EHS) and Process Safety Management (PSM) efforts by ...

... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... Support Environment, Health, and Safety (EHS) and Process Safety Management (PSM) efforts by ...

... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... Support Environment, Health, and Safety (EHS) and Process Safety Management (PSM) efforts by ...

... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... Support Environment, Health, and Safety (EHS) and Process Safety Management (PSM) efforts by ...

Quality Assurance Engineer

Tampa, FL · On-site

$85 - $115/hr

The Quality Assurance Engineer is responsible for ensuring that all turnkey sanitary process ... Experience in the pharmaceutical, biotech, or food processing industry * Hands‑on experience with ...

New

Senior Mechanical Engineer

Miami, FL · On-site

$100 - $120K/hr

... biotechnology? At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work ... Work collaboratively across electrical, optical, fluid, and process engineering fields to design ...

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Showing results 1-20

Biotech Process Engineer information

See Florida salary details

$37K

$68.8K

$106.5K

How much do biotech process engineer jobs pay per year?

As of Aug 19, 2026, the average yearly pay for biotech process engineer in Florida is $68,764.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,700.00 and $77,000.00 per year, depending on experience, location, and employer.

What does a Biotech Process Engineer do?

A Biotech Process Engineer designs, develops, and optimizes processes used in the production of biological products such as pharmaceuticals, vaccines, and biofuels. They work closely with scientists and manufacturing teams to scale up lab procedures to industrial levels while ensuring product quality and regulatory compliance. Their role often involves troubleshooting equipment, improving efficiency, and implementing new technologies within biotech manufacturing environments.

What are the key skills and qualifications needed to thrive as a Biotech Process Engineer, and why are they important?

To thrive as a Biotech Process Engineer, you need a solid background in chemical or biochemical engineering, process design, and regulatory compliance, typically supported by a relevant bachelor's or master's degree. Familiarity with process control systems, bioprocess simulation software, and industry-standard quality systems such as cGMP is essential. Strong analytical thinking, problem-solving abilities, and effective teamwork and communication skills help you excel in cross-functional environments. These skills ensure efficient, compliant, and innovative bioprocess operations, which are critical for product quality and organizational success.

What are some common challenges faced by Biotech Process Engineers during scale-up from laboratory to production?

Biotech Process Engineers often encounter challenges when scaling up processes from laboratory or pilot scale to full production. These challenges can include maintaining product consistency, ensuring process sterility, and adapting equipment to handle larger volumes without compromising yield or quality. Engineers must also collaborate closely with cross-functional teams such as quality assurance, validation, and manufacturing to implement changes efficiently and adhere to regulatory standards. Proactive problem-solving and strong communication skills are key to overcoming these hurdles and ensuring successful technology transfer.

What is the difference between Biotech Process Engineer vs Biotech Manufacturing Technician?

AspectBiotech Process EngineerBiotech Manufacturing Technician
CredentialsBachelor's degree in biotech, chemical engineering, or related field; often requires experience in process designAssociate's or bachelor's degree; focus on operational skills and equipment handling
Work EnvironmentDesigning, optimizing, and overseeing production processes in labs or manufacturing facilitiesOperating and maintaining equipment on the manufacturing floor
Job FocusProcess development, scale-up, troubleshooting, and process improvementExecuting production tasks, quality checks, and equipment setup

Biotech Process Engineers focus on designing and improving manufacturing processes, requiring technical and analytical skills. In contrast, Biotech Manufacturing Technicians handle day-to-day production operations. Both roles are essential in biotech manufacturing but differ in responsibilities and required qualifications.

What job categories do people searching Biotech Process Engineer jobs in Florida look for?

The top searched job categories for Biotech Process Engineer jobs in Florida are:

Infographic showing various Biotech Process Engineer job openings in Florida as of August 2026, with employment types broken down into 70% Full Time, and 30% Contract. Highlights an 94% In-person, and 6% Hybrid job distribution, with an average salary of $68,764 per year, or $33.1 per hour.

Manufacturing Engineer

Stark Pharma Solutions Inc

Orlando, FL • On-site

$68K - $87K/yr

Contractor

Re-posted 5 days ago


Job description

Hi,

My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client and are currently working on a Manufacturing Engineer position. Please send me your updated resume if you have relevant experience and are interested in this opportunity. The detailed job description is as follows.

Job Title: Manufacturing Engineer
Location: Orlando, FL
Duration: Long Term

Position Overview

We are seeking a motivated Manufacturing Engineer with 0–1 year of experience to support manufacturing operations within the pharmaceutical, biotechnology, or medical device industry. This entry-level role is ideal for recent graduates or candidates with internship or co-op experience who are eager to build a career in regulated manufacturing. The selected candidate will assist with process improvements, manufacturing support, equipment qualification, documentation, and quality compliance while working closely with cross-functional teams.

Key Responsibilities

  • Support daily manufacturing operations to ensure safe, efficient, and compliant production.
  • Assist in monitoring and improving manufacturing processes to enhance productivity and product quality.
  • Support equipment installation, qualification, troubleshooting, and maintenance activities.
  • Assist with process validation, equipment qualification (IQ/OQ/PQ), and manufacturing documentation.
  • Prepare and maintain SOPs, work instructions, batch records, and engineering documentation.
  • Collaborate with Manufacturing, Production, Quality Assurance, Validation, Engineering, and Regulatory teams.
  • Collect and analyze manufacturing data to identify process improvement opportunities.
  • Assist with deviation investigations, CAPA activities, and change control documentation.
  • Ensure compliance with GMP, cGMP, FDA regulations, ISO standards, and company quality procedures.
  • Participate in Lean Manufacturing and continuous improvement initiatives.

Required Qualifications

  • Bachelor's degree in Mechanical Engineering, Manufacturing Engineering, Industrial Engineering, Chemical Engineering, Biomedical Engineering, Biotechnology, or a related engineering discipline.
  • 0–1 year of experience through internships, co-op programs, academic projects, or entry-level roles in pharmaceutical, biotechnology, medical device, or regulated manufacturing environments.
  • Basic understanding of manufacturing processes and engineering principles.
  • Familiarity with GMP/cGMP, FDA regulations, ISO 13485, or regulated manufacturing practices is preferred.
  • Basic knowledge of process validation, equipment qualification, and quality systems is a plus.
  • Strong analytical, troubleshooting, and problem-solving skills.
  • Excellent written and verbal communication skills.
  • Ability to work effectively in a cross-functional team environment.
  • Proficiency in Microsoft Office applications.
  • Eagerness to learn and grow in a regulated manufacturing environment.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/