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Bio Recovery Jobs in Florida (NOW HIRING)

Advanced Recovery Systems

Clinical Therapist

Orlando, FL · On-site

$55K - $74K/yr

Join Advanced Recovery Systems (ARS) , an integrated behavioral healthcare management company ... Clinician I will conduct psychosocial and bio-psychosocial assessments. Clinician I will ...

The Recovery Village

IOP Clinical Therapist

Lake Worth, FL · On-site

$52K - $71K/yr

Monday- Thursday 11am-9pm The Recovery Village Palm Beach at Baptist Health is a center that ... The IOP Clinician will conduct psychosocial and bio-psychosocial assessments. This Clinician will ...

The Recovery Village

IOP Clinical Therapist

Lake Worth, FL · On-site

$52K - $71K/yr

Monday- Thursday 11am-9pm The Recovery Village Palm Beach at Baptist Health is a center that ... The IOP Clinician will conduct psychosocial and bio-psychosocial assessments. This Clinician will ...

The Recovery Village

IOP Clinical Therapist

Lake Worth, FL · On-site

$52K - $71K/yr

Monday- Thursday 11am-9pm The Recovery Village Palm Beach at Baptist Health is a center that ... The IOP Clinician will conduct psychosocial and bio-psychosocial assessments. This Clinician will ...

The Recovery Village

Clinical Therapist

Orlando, FL · On-site

$55K - $74K/yr

Join Advanced Recovery Systems (ARS) , an integrated behavioral healthcare management company ... Clinician I will conduct psychosocial and bio-psychosocial assessments. Clinician I will ...

Lakeview Health

Therapist

Jacksonville, FL · On-site

Lakeview Health has helped thousands of people detox, recover and remain abstinent from dangerous ... Conduct comprehensive bio-psycho-social assessments with newly admitted patients * Assess and ...

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Bio Recovery information

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How much do bio recovery jobs pay per hour?

As of Aug 28, 2026, the average hourly pay for bio recovery in Florida is $13.38, according to ZipRecruiter salary data. Most workers in this role earn between $11.49 and $14.38 per hour, depending on experience, location, and employer.

What is a bio recovery technician?

Bio recovery technicians are professionals trained to safely clean, disinfect, and remove hazardous biological materials from crime scenes, accidents, trauma incidents, or locations affected by infectious diseases. Their work involves handling substances like blood, bodily fluids, and other potentially infectious materials, ensuring that sites are fully restored to a safe condition. They follow strict safety protocols and use specialized equipment and cleaning agents to prevent the spread of pathogens. Bio recovery technicians often work in emotionally challenging environments and must adhere to legal and health regulations.

What skills and qualifications are needed to thrive as a bio recovery technician?

To thrive as a Bio Recovery Technician, you need training in hazardous material handling, knowledge of OSHA regulations, and often a certification in biohazard cleanup or crime scene cleaning. Familiarity with personal protective equipment (PPE), cleaning/disinfection chemicals, and specialized decontamination tools is typically required. Attention to detail, emotional resilience, and strong communication skills are essential for both safety and supporting affected individuals. These skills are crucial to ensure thorough, compliant, and compassionate cleanup in environments exposed to biological hazards.

What are common challenges faced by bio recovery professionals, and how are they addressed on the job?

Bio Recovery professionals often encounter emotionally challenging and hazardous situations, such as crime scenes, trauma incidents, or unattended deaths. These challenges require strict adherence to safety protocols, use of personal protective equipment, and strong emotional resilience. Teamwork and ongoing training are essential, as professionals frequently collaborate to ensure thorough cleaning, compliance with regulations, and support for affected environments. Employers typically offer mental health resources and support systems to help staff cope with the demanding nature of the work.

What is the difference between Bio Recovery vs Biohazard Technician?

AspectBio RecoveryBiohazard Technician
CertificationsBloodborne Pathogens, OSHA trainingBloodborne Pathogens, OSHA training
Work EnvironmentCrime scenes, accident sites, trauma scenesCrime scenes, trauma scenes, infectious disease cleanup
Industry UsageCrime scene cleanup, trauma scene remediationBiohazard cleanup, infectious disease decontamination

Bio Recovery specialists and Biohazard Technicians often perform similar tasks in cleaning and disinfecting biohazardous scenes. Both roles require certifications like Bloodborne Pathogens training and work in similar environments such as crime and trauma scenes. However, Bio Recovery typically emphasizes trauma scene cleanup and recovery services, while Biohazard Technicians may focus more broadly on infectious disease decontamination and hazardous material handling.

Do you need a degree to do bio recovery?

Bio recovery technicians typically do not need a college degree but must complete specialized training and certifications in biohazard handling, safety procedures, and sanitation. Employers often prioritize experience, attention to detail, and adherence to safety protocols over formal education.

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

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

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

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

Bio Recovery jobs near you
Infographic showing various Bio Recovery job openings in Florida as of August 2026, with employment types broken down into 81% Full Time, and 19% Part Time. Highlights an 100% In-person job distribution, with an average salary of $27,825 per year, or $13.4 per hour.

Manufacturing Associate III

Kincell Bio, LLC

Gainesville, FL • On-site

Full-time

Posted 5 days ago

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.
Kincell is seeking a highly motivated Associate III who will be a key contributor to a dynamic and collaborative Manufacturing team. We offer challenging career opportunities, competitive benefits and an environment that recognizes and rewards performance. As an Associate III, you will be operating automatic and manual cell therapy equipment with a variety of complexity 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 a team member who is 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. You will contribute to the team's success by sharing knowledge. Patients need colleagues like you who take pride in their work and look for successful outcomes. You will help ensure patients have the therapies they need when they need them. You will be operating cell therapy process equipment of varying complexity with different processes in accordance with standard operating procedures.
Essential Duties and Responsibilities
Reasonable accommodation 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.
  • Independently execute and oversee complex GMP manufacturing operations under approved SOPs and Master Batch Records (MBRs), serving as a senior technical resource on the manufacturing floor.
  • Perform and lead high-risk and critical manufacturing steps, including complex aseptic manipulations, open processing, formulation, and final drug product fill activities.
  • Demonstrate advanced proficiency with manufacturing equipment relevant to cell and gene therapy processing, including setup, execution, basic troubleshooting, and readiness verification.
  • Act as a technical point-of-contact during GMP operations, supporting issue resolution, real-time decision-making, and escalation as needed.
  • Maintain and demonstrate aseptic technique qualification and serve as a role model for cleanroom behavior, contamination control, and GMP discipline.
  • Ensure manufacturing activities are executed Right-the-First-Time, identifying and correcting errors proactively before QA intervention.
  • Perform and independently verify complex calculations (dilutions, yields, recoveries, volumes) and assess process outcomes for accuracy and compliance.
  • Author and lead manufacturing deviations, including root cause analysis (5M / 5-Why), impact assessments, and proposed corrective actions, with QA partnership.
  • Support and, when assigned, own manufacturing-driven Change Controls, including technical justifications, execution readiness, and implementation support.
  • Support and execute CAPAs, ensuring actions are practical, effective, and sustainable on the manufacturing floor.
  • Demonstrate strong application of Good Documentation Practices (GDP) across paper-based and electronic systems.
  • Identify systemic risks, recurring issues, and process gaps, and proactively escalate improvement opportunities.
  • Serve as a subject-matter resource during audits, inspections, and internal quality reviews as applicable
  • Serve as a Qualified Trainer for multiple tasks, equipment, or procedures, including aseptic qualification and complex manufacturing operations.
  • Mentor Manufacturing Associate I and II personnel, providing technical coaching, feedback, and development support.
  • Support onboarding, qualifications, and readiness of new hires and newly qualified associates.
  • Contribute to the design, refinement, and continuous improvement of training curricula, OJTs, and qualification pathways.
  • Provide day-to-day floor leadership, coordinating execution activities and supporting shift or campaign readiness in the absence of formal supervision.
  • Collaborate cross-functionally with QA, MSAT, Engineering, Supply Chain, and QC to resolve issues and ensure execution readiness.
  • Lead or significantly contribute to continuous improvement initiatives, process optimizations, and risk reduction efforts.
  • Provide technical input and review for SOPs, MBRs, Work Instructions, and protocols, ensuring clarity, compliance, and execution feasibility.
  • Support batch readiness activities, pre-campaign equipment verification, and 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:
  • Education and Experience (one of the following):
    • Bachelor's Degree (BS) in Natural Sciences (e.g., Biology, Chemistry, Life Sciences) or Engineering (Chemical, Biomedical, or related) with a minimum of 2+ years of relevant GMP manufacturing experience.
    • Associate's degree (AS) in Life Sciences, Engineering, or related discipline with a minimum of 3+ years of relevant GMP manufacturing experience.
    • High School Diploma (or equivalent) with a minimum of 5+ years of relevant GMP manufacturing or regulated technical experience.
  • Demonstrated ability to lead and execute complex GMP manufacturing operations independently.
  • Must be able to work 40 hours per week. Overtime will be required frequently to meet production needs.
  • Ability to adapt to changing priorities, production schedules, and operational demands.
  • Strong proficiency in Microsoft Excel, Word, and PowerPoint for documentation, data review, investigations, and operational tracking.
  • Strong written and verbal communication skills suitable for deviation authorship, technical discussions, and cross-functional collaboration.
  • Proven ability to identify, investigate, and resolve manufacturing and compliance issues.
  • Ability to meet physical requirements of the role, including lifting materials/media and standing or sitting for extended periods.
  • Successful completion of visual acuity requirements, as applicable.

Preferred:
  • B.S degree in Natural Sciences (i.e, Biology, Chemistry, etc.) or Engineering (Chemical, Biomedical, etc.) and 3+ years of manufacturing experience.
  • Experience working within electronic Quality Management Systems (QMS) (e.g., Veeva Vault) for deviations, CAPAs, training, and document control.
  • Prior experience owning or leading Change Controls in a GMP manufacturing environment.
  • Experience supporting regulatory inspections, audits, or client-facing reviews.
  • Advanced experience in cell and gene therapy manufacturing, aseptic processing, or complex cell culture platforms.
  • Demonstrated leadership in process improvement, risk assessments, or operational excellence initiatives.
  • Experience working in cGMP cleanroom environments (ISO 5-8)

Travel Requirements
  • Little to none

Physical Demands
  • Adjusting or moving objects weighing up to 50lbs
  • Vision Acuity Testing
  • Use of a Face Mask

Location
  • This is a site-based 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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