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Biotech Quality Control Jobs in Florida (NOW HIRING)

TekWissen LLC

Quality Assurance Engineer

Tampa, FL · On-site

$25 - $35/hr

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 ...

Alphazyme

Manager, QA Operations

Jupiter, FL

Support Quality Control with customer complaints and Out of Specification (OOS) investigations ... non-academic biotechnology related industry * 1-3 years of supervisory experience * Proven ...

Vhr_unither

Senior Quality Engineer

Jacksonville, FL · On-site

$82K - $111K/yr

The job details are as follows: Who We Are We are the first publicly-traded biotech or ... Who You Are The Senior Quality Control Engineer performs activities supporting the full equipment ...

Danaher

Senior Quality Engineer

Pensacola, FL

$83K - $113K/yr

... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... Ensure design control process compliance throughout the product lifecycle and deliver training on ...

Danaher

Senior Quality Engineer

Pensacola, FL · On-site

$83K - $113K/yr

... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... Ensure design control process compliance throughout the product lifecycle and deliver training on ...

Danaher

Quality Inspector II

New Port Richey, FL

$29 - $32/hr

... and biotechnology? At Pall Corporation, one of Danaher's 15+ operating companies, our work saves ... This position reports to the Quality Control Inspection Manager. This position requires access to ...

Danaher

Senior Quality Engineer (Sunday-Thursday)

Pensacola, FL · On-site

$83K - $113K/yr

... biotechnology? At Cytiva, one of Danaher's 15+ operating companies, our work saves lives-and we're ... Directed process validation and control strategies (IQ/OQ/PQ, SPC), improving process capability ...

Danaher

Quality Inspector II

New Port Richey, FL · On-site

... and biotechnology? At Pall Corporation, one of Danaher's 15+ operating companies, our work saves ... This position reports to the Quality Control Inspection Manager. This position requires access to ...

Danaher

Quality Inspector II

New Port Richey, FL

... and biotechnology? At Pall Corporation, one of Danaher's 15+ operating companies, our work saves ... This position reports to the Quality Control Inspection Manager. This position requires access to ...

Danaher

Quality Inspector II

New Port Richey, FL · On-site

... and biotechnology? At Pall Corporation, one of Danaher's 15+ operating companies, our work saves ... This position reports to the Quality Control Inspection Manager. This position requires access to ...

Danaher

Quality Inspector II

New Port Richey, FL

... and biotechnology? At Pall Corporation, one of Danaher's 15+ operating companies, our work saves ... This position reports to the Quality Control Inspection Supervisor. This position requires access ...

Danaher

Quality Inspector II

New Port Richey, FL · On-site

... and biotechnology? At Pall Corporation, one of Danaher's 15+ operating companies, our work saves ... This position reports to the Quality Control Inspection Manager. This position requires access to ...

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Showing results 21-40

All JobsBiotech Quality Control JobsBiotech Quality Control Jobs in Florida

Biotech Quality Control information

See Florida salary details

$22.8K

$60.8K

$96.8K

How much do biotech quality control jobs pay per year?

As of Aug 9, 2026, the average yearly pay for biotech quality control in Florida is $60,772.00, according to ZipRecruiter salary data. Most workers in this role earn between $45,200.00 and $74,700.00 per year, depending on experience, location, and employer.

What does a biotech quality control do?

On a daily basis, a Biotech Quality Control professional performs routine testing and analysis of raw materials, intermediates, and finished products to ensure they meet established specifications. This involves preparing samples, operating analytical equipment, maintaining accurate records, and documenting results in compliance with regulatory guidelines. Quality Control staff also collaborate closely with production, quality assurance, and research teams to troubleshoot issues and support process improvements. Regular internal audits and participation in team meetings are common, making communication and teamwork key parts of the job.

What is a biotech quality control?

A Biotech Quality Control (QC) job involves ensuring that biological products, processes, and facilities meet regulatory and quality standards. QC professionals conduct testing, analyze data, and document results to verify product safety and efficacy. They work with laboratory techniques such as PCR, HPLC, and microbiological testing. The role is critical in maintaining compliance with industry regulations like GMP and FDA guidelines.

What are the key skills and qualifications needed to thrive in biotech quality control?

To excel in Biotech Quality Control, candidates typically need a background in biology, chemistry, or related sciences, with strong knowledge of laboratory techniques and regulatory requirements. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and common analytical instruments such as HPLC or PCR is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this role. These competencies are vital for ensuring that biotech products consistently meet quality and compliance standards essential for patient safety and regulatory approval.

What are the most commonly searched types of Biotech Quality Control jobs in Florida? The most popular types of Biotech Quality Control jobs in Florida are:
What are popular job titles related to Biotech Quality Control jobs in Florida? For Biotech Quality Control jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Biotech Quality Control jobs in Florida look for? The top searched job categories for Biotech Quality Control jobs in Florida are:
What cities in Florida are hiring for Biotech Quality Control jobs? Cities in Florida with the most Biotech Quality Control job openings:
Biotech Quality Control jobs near you
Infographic showing various Biotech Quality Control job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, 1% Temporary, 3% Contract, and 2% Nights. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $60,772 per year, or $29.2 per hour.

Quality Assurance Engineer

TekWissen LLC

Tampa, FL • On-site

$25 - $35/hr

Temporary

Re-posted 13 days ago

Job description

Overview:  
 
TekWissen group is a workforce management provider throughout the USA and many other countries in the world. Our client is a leading biotechnology company that combines technological expertise with world-class manufacturing and scientific insight to support the delivery of innovative medicines for a wide range of diseases. Specializing in pharmaceutical ingredients, bioscience, biopharmaceuticals, custom manufacturing, and cell and gene therapy, the company provides comprehensive services across the pharmaceutical, biotech, and life sciences sectors. It supports every stage of drug development, from early research to commercial production, and offers solutions in biologics, small molecules, and specialty ingredients. Committed to quality and innovation, the company serves as a critical partner in advancing therapeutic solutions and streamlining complex manufacturing processes, with a global presence that ensures access to scalable, flexible, and compliant technical expertise.
 
 
Job Title:        Quality Assurance Engineer
Location:        Tampa, FL - 33634
Duration:        12 months 
Job Type:        Temporary Position
Work Type:    Onsite
 
 
Summary
 
The QA Engineer is responsible for ensuring the timely development, review, and approval of engineering, validation, and lifecycle documentation in compliance with corporate procedures, SOPs, cGMP standards, and industry best practices. This role supports validation activities across the full lifecycle and ensures the facility remains inspection-ready and compliant.
Work Model: 100% On-site.
 
Responsibilities:
  • Review and approve engineering and validation documentation, including IQ, OQ, PQ, and PPQ protocols, validation master plans, risk assessments, calibration, and periodic reviews.
  • Collaborate with plant and external engineering teams to ensure new installations, systems, and commissioning documentation comply with cGMP requirements.
  • Support the full Validation Lifecycle from design through operational improvements and revalidation programs.
  • Represent QA in cross-functional teams supporting production facility build-outs and laboratory move activities (commissioning, validation, CSV).
  • Create, review, and approve SOPs, Change Controls, CAPAs, deviations, forms, reports, and other quality system documentation.
  • Partner with internal and external stakeholders to provide quality validation support aligned with project and regulatory requirements.
  • Interface with Manufacturing, Packaging, Engineering, MSAT, PD, and QA/QC teams to resolve process issues and implement changes.
  • Conduct risk identification and management throughout the product lifecycle using risk management tools.
  • Support deviation investigations related to manufacturing equipment, utilities, automation, computer systems, validation, and laboratory instruments.
  • Contribute to continuous improvement initiatives within GMP Validation and Change Control programs.
  • Participate in internal, client, and regulatory audits.
  • Ensure the site maintains cGMP compliance and inspection readiness.
  • Establish, maintain, trend, and report Quality KPIs and metrics.
  • Participate in Management Review, Quality Review Board, Deviation Review Board, and Change Review Board meetings.
  • Perform additional duties as assigned by the Senior Manager of QA Operations.
Required Qualifications
  • Strong knowledge of cGMP regulations and compliance requirements.
  • Hands-on experience with validation processes (IQ, OQ, PQ, PPQ).
  • Experience reviewing and approving validation and engineering documentation.
  • Proficiency in Change Control, CAPA, Deviations, and Quality Systems documentation.
  • Understanding of Validation Lifecycle and revalidation processes.
  • Experience supporting audits (internal, client, regulatory).
  • Risk management knowledge and application in GMP environments.
  • Cross-functional collaboration and stakeholder management skills.
  • Strong analytical, documentation, and problem-solving skills.
  • Experience supporting facility start-up, commissioning, or laboratory relocations.
  • Exposure to computerized system validation (CSV).
  • Experience in biologics, pharmaceutical, or medical device manufacturing environments.
  • Knowledge of KPI tracking, trending, and quality metrics reporting.
  • Continuous improvement mindset and experience in quality system enhancement initiatives.
TekWissen® Group is an equal opportunity employer supporting workforce diversity.

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.

TekWissen® is an equal opportunity employer supporting workplace diversity. 

TekWissen logo

About TekWissen

Sourced by ZipRecruiter

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Ann Arbor, MI, US

Year founded

2009

Social media

Twitter

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