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Bio Manufacturing Jobs in Florida (NOW HIRING)

Kincell Bio, LLC

Office Coordinator

Gainesville, FL · On-site

$16.25 - $21.75/hr

Kincell Bio engineers cells into therapies. With manufacturing facilities located in Research Triangle Park, NC and Gainesville, FL, Kincell Bio is a contract development and manufacturing ...

ARTHREX

Product Management, Bio/Wound

Naples, FL

Product Management, Bio/Wound Arthrex, Inc. is a global medical device company and a leader in new ... manufacturing coordination for new and emerging products. * Coordinates technical product ...

Arthrex

Product Management, Bio/Wound

Naples, FL · On-site

Product Management, Bio/Wound Arthrex, Inc. is a global medical device company and a leader in new ... manufacturing coordination for new and emerging products. * Coordinates technical product ...

Accurate Biomed Services, Inc

Technician

Ocala, FL

$23.50 - $31.25/hr

Manufacturer certifications and/or experience on oxygen concentrator units or bio-medical equipment highly preferred but we will train and certify the right individuals. Additional Information All ...

Accurate Biomed Services, Inc

Technician

Ocala, FL · On-site

$23.50 - $31.25/hr

Manufacturer certifications and/or experience on oxygen concentrator units or bio-medical equipment highly preferred but we will train and certify the right individuals. Qualifications Additional ...

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All JobsBio Manufacturing JobsBio Manufacturing Jobs in Florida

Bio Manufacturing information

See Florida salary details

$26.5K

$59.7K

$84.1K

How much do bio manufacturing jobs pay per year?

As of Aug 27, 2026, the average yearly pay for bio manufacturing in Florida is $59,667.00, according to ZipRecruiter salary data. Most workers in this role earn between $53,100.00 and $66,500.00 per year, depending on experience, location, and employer.

What is bio manufacturing?

Bio manufacturing, also known as biomanufacturing, is the process of using biological systems like cells or enzymes to produce commercial products such as medicines, vaccines, biofuels, and food ingredients. This field combines biology, engineering, and technology to create products in a controlled and scalable way, often using fermentation or cell culture techniques. Biomanufacturing plays a critical role in the pharmaceutical, biotechnology, and food industries, enabling the production of complex molecules that are difficult to synthesize chemically. Professionals in this field work on developing, optimizing, and scaling up these biological processes to ensure high-quality and cost-effective product output.

What are the key skills and qualifications needed to thrive in bio manufacturing?

To thrive in Bio Manufacturing, you need a solid background in biology, chemistry, or engineering, often supported by a relevant degree or certification. Familiarity with Good Manufacturing Practices (GMP), bioprocessing equipment, and quality control systems is typically required. Attention to detail, problem-solving abilities, and strong teamwork skills help individuals excel in this environment. These competencies are crucial for ensuring product quality, regulatory compliance, and efficient production in the biotechnology industry.

What are some common challenges faced by professionals working in bio manufacturing, and how can they be addressed?

Professionals in bio manufacturing often encounter challenges such as maintaining strict quality control standards, adapting to rapidly evolving technologies, and ensuring compliance with regulatory requirements. Addressing these challenges involves continuous training, staying updated on industry best practices, and fostering strong communication within cross-functional teams. Many companies also encourage ongoing professional development and provide resources to help employees stay current with regulations and technological advancements.

What is the difference between Bio Manufacturing vs Bioprocess Technician?

AspectBio ManufacturingBioprocess Technician
CredentialsTypically requires a Bachelor's degree in Biotechnology, Biology, or related fieldOften requires a diploma or associate degree in Biotechnology or related field
Work EnvironmentManufacturing facilities, laboratories, cleanroomsProduction floors, laboratories, cleanrooms
Industry UsageUsed broadly across biotech, pharmaceutical, and biopharmaceutical companiesPrimarily in biotech and pharmaceutical manufacturing
Job FocusOversees entire manufacturing processes, quality control, and compliancePerforms specific tasks in bioprocessing, equipment operation, and sample testing

Bio Manufacturing involves overseeing the entire production process in biotech and pharmaceutical industries, often requiring higher-level degrees and responsibilities. Bioprocess Technicians focus on executing specific bioprocessing tasks, typically with technical diplomas. Both roles work in similar environments but differ in scope and qualifications.

What are popular job titles related to Bio Manufacturing jobs in Florida?

For Bio Manufacturing jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Bio Manufacturing jobs in Florida look for?

The top searched job categories for Bio Manufacturing jobs in Florida are:

Bio Manufacturing jobs near you
Infographic showing various Bio Manufacturing job openings in Florida as of August 2026, with employment types broken down into 89% Full Time, and 11% Contract. Highlights an 100% In-person job distribution, with an average salary of $59,667 per year, or $28.7 per hour.

Manufacturing Associate I, Contingent Worker

Kincell Bio, LLC

Gainesville, FL • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Kincell Bio engineers cells into therapies. With manufacturing facilities located in Research Triangle Park, NC and Gainesville, FL, Kincell Bio is a contract development and manufacturing organization (CDMO) with the mission to streamline CMC development, apply expertise in analytical and process development and GMP manufacturing, testing and release from early clinical to pivotal studies and product launch. Kincell Bio is focused on supporting innovative companies developing immune cell therapies, including autologous and allogeneic CAR-T, TCR, TILs, Tregs and CAR-NK technologies. We offer challenging career opportunities, competitive benefits, and an environment that recognizes and rewards performance.
For more information, please visit our website at www.kincellbio.com.
As a Contingent Manufacturing Associate I, you will be operating automatic and manual cell and gene therapy equipment with a variety of complexities in CAR-T, CAR-M, or CAR-NK processes in accordance with standard operating procedures and policies. You will perform quality control analyses as required to complete in-process batches and identify variations. You will be trained in handling hazardous materials and emergency procedures since you will be handling leukapheresis cellular materials.
As part of manufacturing operations, you will be relied on to have a good understanding of procedures, techniques, tools, materials, and equipment. Your work and decision-making will be team-based and will focus on the prioritization of workflows centered on the process and available resources. You will follow standard operating procedures to complete tasks which may vary in scope, complexity, and timing.
Patients need individuals who take pride in their work and look for successful outcomes. You will be operating cell and gene therapy process equipment of varying complexity with different processes in accordance with standard operating procedures.
Essential Duties and Responsibilities
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.This list contains the major duties and requirements of the job and is not all-inclusive. Incumbent(s) may be expected to perform role-related duties other than those contained in this document.
  • Working knowledge of Word and Excel
  • Demonstrate Aseptic Qualification
  • Maintaining personal responsibility with Personal Protective Equipment (PPE)
  • Be a collaborator when a team develops Standard Operating Procedures or Manufacturing Batch Records
  • Conduct Quality Control analyses in a Manufacturing setting
  • Able to learn how to handle materials and bring them into a Manufacturing cleanroom.
  • Clean Equipment and Manufacturing Suite / Rooms
  • Be accountable for your own Safety. Also, be accountable for maintaining your own training requirements.
  • Collaborate with the Investigation team when investigating Quality and Safety Incidents
  • Author Minor Quality / Safety Incident Investigation (Deviations) and Minor CAPAs
  • Develop a knowledge of GXP procedures (GMP, GLP, GCP, GDP, etc.)
  • Must help with cleaning with Equipment and Manufacturing process rooms.
  • Contribute to the team's success by sharing knowledge.
  • Review of Applicable Logbooks
  • Support and Conduct Enrollment of Materials / Bill of Materials.
  • Create Purchase Requests / Procuring Items as needed.
  • Escort Vendors / Visitors into the cleanroom
  • Conduct post-campaign line or area clearance

Qualifications
The requirements listed below are representative of the knowledge, skill, and/or ability required to perform this job successfully.
Required:
  • Bachelor of Science degree in Natural Sciences (i.e., Biology, Chemistry, etc.) or Engineering (Chemical, Biomedical, etc.) and 0-2 years of manufacturing experience required or equivalent combination of education and experience.
  • Must be able to work 40 hours per week.
  • Ability to work independently and stay on task in a fast-paced environment without direct supervision.
  • Must be able to recognize when processes, procedures, equipment, products, materials, etc. are out of specification.
  • Hiring will be contingent on passing a visual acuity test. Proof of passing a visual acuity test within the past year will be accepted
  • Effective oral communication.
  • Ability to work well with others in a collaborative team environment.
  • Regular and reliable performance and attendance are required.
  • Able to work in a rapidly changing climate - reacts well to change.
  • Must be able to perform mathematical calculations such as converting milliliters to liters or grams to kilograms. Understands significant figures and rounding.
  • Must be able to lift bags and/or containers of media.
  • Must be able to stand and/or sit for extended periods.
  • Manage your own time and professional development. Be accountable for your own results and prioritized workflows.

Preferred:
  • Have knowledge of cell and gene therapy processing, the metric system, and scales.
  • cGMP clean room experience.

Physical Requirements
  • Vision Acuity Testing
  • Use of a Face Mask

Travel Requirements
  • None

Location
  • This is a site-based temporary position located in Gainesville, FL, and will require some non-standard working hours, including scheduled early mornings, late evenings, and/or weekends.

#LI-Onsite
Kincell Bio provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable, federal, state, and local laws. Kincell Bio complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.
NOTE TO EMPLOYMENT AGENCIES: Kincell Bio values our relationships with our Recruitment Partners. We will only accept resumes from those partners who have been contracted by a member of our Human Resources team to collaborate with us. We are not responsible for any fees related to resumes that are unsolicited or are received without contract.

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