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Qc Biotech Jobs in Florida (NOW HIRING)

QC Microbiologist

Seminole, FL · On-site

$85K - $87K/yr

Quality Control Microbiology Supervisor Overview: Quality Control (QC) Microbiology Supervisor ... Minimum 5 years of hands-on experience in a cGMP pharmaceutical or biotech microbiology laboratory ...

QC Stability Coordinator

Tampa, FL · On-site

$18.75 - $25.75/hr

QC Stability Coordinator Location: Tampa, FL (on-site) Today, Lonza is a global leader in life ... Experience in a regulated environment such as pharmaceutical, biotech, or laboratory settings.

QC Stability Coordinator

Tampa, FL · On-site

$18.75 - $25.75/hr

QC Stability Coordinator Location: Tampa, FL (on-site) Today, Lonza is a global leader in life ... Experience in a regulated environment such as pharmaceutical, biotech, or laboratory settings.

Quality Control Analyst I

Sunrise, FL · On-site

$23 - $30.75/hr

... biotechnology or environmental laboratory o Experience to Labware LIMS V7 and laboratory auditing ... Quality Control Laboratory environment. Requires working knowledge of cGMP, DEA and other ...

Quality Control Lab Technician III

Pensacola, FL · On-site +1

$18.75 - $23.75/hr

... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... The QC Lab Technician III is responsible for conducting routine and non-routine analysis of raw ...

Quality Control Lab Technician III

Pensacola, FL · On-site

$18.75 - $23.75/hr

... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... The QC Lab Technician III is responsible for conducting routine and non-routine analysis of raw ...

Client is seeking an entry-level Quality Assurance / Quality Control Associate to support clinical ... This is a great opportunity for individuals looking to begin their careers in biotech, particularly ...

Assistant Data Entry/Quality Control

Miami, FL · On-site

$16 - $21.25/hr

The Assistant Data Entry/Quality Control staff member completes electronic case report forms by ... Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device ...

Assistant Data Entry/Quality Control

Miami, FL · On-site

$16 - $21.25/hr

The Assistant Data Entry/Quality Control staff member completes electronic case report forms by ... Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device ...

Maravai LifeSciences translates extraordinary science into everyday miracles, helping biotech ... Support Quality Control with customer complaints and Out of Specification (OOS) investigations

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 ...

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Qc Biotech information

What is a QC Biotech?

A QC (Quality Control) Biotech professional is responsible for ensuring that biotechnology products, such as pharmaceuticals, vaccines, or biologics, meet strict quality and safety standards. They perform laboratory tests, analyze samples, and document results to ensure compliance with regulatory guidelines. QC Biotech professionals play a crucial role in maintaining the integrity of products before they reach the market, working closely with other departments to resolve any quality issues. Their work helps protect patient safety and supports the success of biotech companies.

What are the key skills and qualifications needed to thrive as a QC Biotech?

To thrive as a QC Biotech, you need a solid background in biology, chemistry, and laboratory techniques, usually supported by a degree in life sciences or a related field. Familiarity with analytical instruments such as HPLC, PCR, and ELISA, as well as GMP regulations and LIMS software, is typically required. Attention to detail, strong problem-solving abilities, and effective teamwork are crucial soft skills for this role. These skills and qualities ensure accurate testing, regulatory compliance, and the integrity of biotechnological products.

What are some common challenges faced by QC Biotech professionals and how can they be addressed?

QC Biotech professionals often encounter challenges such as adapting to rapidly changing regulatory standards, troubleshooting complex assay discrepancies, and maintaining precise documentation under tight deadlines. Addressing these challenges requires continuous learning, strong attention to detail, and effective collaboration with cross-functional teams like R&D and manufacturing. Leveraging robust Standard Operating Procedures and clear communication with colleagues can help ensure consistent results and regulatory compliance.

What is the difference between Qc Biotech vs Qc Microbiologist?

AspectQc BiotechQc Microbiologist
Required CredentialsBachelor's in Biology, Biotechnology, or related field; GMP/GxP trainingBachelor's in Microbiology, Biology, or related; microbiology certifications
Work EnvironmentBiotech manufacturing labs, quality control departmentsMicrobiology labs, pharmaceutical or biotech settings
Employer & Industry UsageBiotech companies, pharmaceutical manufacturersPharmaceutical firms, biotech research labs
Common Search & ComparisonYesYes

While both Qc Biotech and Qc Microbiologist roles involve quality testing in biotech and pharmaceutical settings, Qc Biotech focuses on overall product quality, including assays and validation, whereas Qc Microbiologists specialize in microbiological testing and contamination control. The roles often overlap but differ in specific expertise and focus areas.

Infographic showing various Qc Biotech job openings in Florida as of August 2026, with employment types broken down into 2% As Needed, 86% Full Time, 7% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 93% Physical, 4% Hybrid, and 3% Remote job distribution.

QC Microbiologist

Eagle Labs, Inc

Seminole, FL • On-site

$85K - $87K/yr

Full-time

Posted 23 days ago


Job description

Quality Control Microbiology Supervisor

Overview:

Quality Control (QC) Microbiology Supervisor oversees daily microbiology laboratory operations and a team of analysts. They ensure all testing—such as sterility, bioburden, endotoxin, and environmental monitoring—complies with strict adherence to the GMP regulations. This role spans method validation, root-cause investigations, and data integrity verification.

Key Duties:

These are only highlighted by major key duties. Other requested duties assigned by Eagle Labs, Inc for job function by Quality Control Manager, Director of Laboratory Operations, or Executive leadership.

  • Scheduling, conducting OOS (Out-of-Specification) investigations, and managing staff training scheduling, conducting investigations, and managing staff training.
  • Supervises routine testing, including sterility testing, bacterial endotoxins (BET), bioburden, microbial limits, and growth promotion of media.
  • Support assay method verification, transfer, and equipment qualification within the Laboratory.
  • Act as a subject matter expert (SME) during internal audits and regulatory inspections.
  • Lead Out-of-Specification (OOS) investigations, initiate Corrective and Preventive Actions (CAPA), and implement change controls.

Core Responsibilities:

  • Team Leadership & Development: Supervise, train, and mentor laboratory analysts. Manage scheduling, performance evaluations, and gowning/aseptic qualifications.
  • Testing Oversight: Oversee and review routine microbiological assays, including sterility, bioburden, bacterial endotoxins (LAL), microbial identification (e.g., MALDI-TOF), and water testing.
  • Environmental Monitoring (EM): Approve EM data, analyze trending reports, and monitor classified cleanroom utilities to maintain compliance.

Qualifications & Requirements

  • Education: Bachelor’s degree in microbiology, Biology, or a closely related life science discipline.
  • Experience: Minimum 5 years of hands-on experience in a cGMP pharmaceutical or biotech microbiology laboratory, including at least 3 or more years in a lead or supervisory capacity.
  • Technical Skills: Advanced understanding of aseptic processing, cleanroom behaviors, and compendial requirements (USP, EP, JP).
  • Soft Skills: Strong problem-solving, data trending capabilities, and excellent verbal and written communication skills.