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Process Development Cell Gene Therapy Jobs in Florida

TekWissen LLC

Quality Assurance Engineer

Tampa, FL · On-site

$25 - $35/hr

... cell and gene therapy, the company provides comprehensive services across the pharmaceutical ... It supports every stage of drug development, from early research to commercial production, and ...

TekWissen LLC

Packaging Operator I

Tampa, FL · On-site

$15 - $20/hr

... process excellence and helps their customers to deliver new and innovative medicines that help ... cell and gene therapy. Job Title: Packaging Operator I Location: Tampa, FL, 33634 Duration: 12 ...

TekWissen LLC

Packaging Operator I

Tampa, FL · On-site

$20 - $24/hr

... process excellence and helps their customers to deliver new and innovative medicines that help ... cell and gene therapy. Job Title: Packaging Operator I Location: Tampa, FL, 33634 Duration: 12 ...

Socket.dev

Senior Manufacturing Engineer

Pensacola, FL · On-site

$90 - $120/hr

... cell and gene therapies. At Cytiva, you will be able to continuously improve yourself and us ... process, product, manufacturing, quality engineering, R&D, or product development. * Hands-on ...

New

TekWissen LLC

Packaging Operator III

Tampa, FL · On-site

$18 - $20/hr

... process excellence and helps their customers to deliver new and innovative medicines that help ... cell and gene therapy. Job Title: Packaging Operator III Location: Tampa, FL, 33634 Duration: 12 ...

TekWissen LLC

Packaging Operator I

Tampa, FL · On-site

$15 - $20/hr

... process excellence and helps their customers to deliver new and innovative medicines that help ... cell and gene therapy. Job Title: Packaging Operator I Location: Tampa, FL, 33634 Duration: 12 ...

Alphazyme

Manager, QA Operations

Jupiter, FL · On-site

... cell and gene therapy companies. At Maravai, we believe that diverse perspectives are the ... Collaborate with management to identify and fill documentation and process gaps required to ...

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All JobsProcess Development Cell Gene Therapy JobsProcess Development Cell Gene Therapy Jobs in Florida

Process Development Cell Gene Therapy information

What is the difference between Process Development Cell Gene Therapy vs Process Development Associate?

AspectProcess Development Cell Gene TherapyProcess Development Associate
CredentialsBachelor's/Master's in Biotechnology, Molecular Biology, or related fields; experience in cell therapy preferredBachelor's/Master's in Life Sciences; entry-level to mid-level experience in bioprocessing
Work EnvironmentLaboratories focused on cell therapy manufacturing, GMP facilitiesBiotech or pharmaceutical labs, manufacturing support roles
Industry UsagePrimarily in cell and gene therapy companies, biotech firmsBroadly in biotech, pharma, and contract manufacturing organizations

The Process Development Cell Gene Therapy role specializes in developing and optimizing processes for cell-based gene therapies, often requiring specific expertise in cell culture and GMP compliance. In contrast, the Process Development Associate has a broader scope, supporting various bioprocessing activities across different products. Both roles require strong laboratory skills, but the Cell Gene Therapy position emphasizes specialized knowledge in cell therapy manufacturing.

What are popular job titles related to Process Development Cell Gene Therapy jobs in Florida? For Process Development Cell Gene Therapy jobs in Florida, the most frequently searched job titles are:
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Process Development Cell Gene Therapy jobs near you

Quality Assurance Engineer

TekWissen LLC

Tampa, FL • On-site

$25 - $35/hr

Temporary

Re-posted 15 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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