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Temp Change Control Jobs in Florida (NOW HIRING)

TekWissen LLC

Quality Assurance Engineer

Tampa, FL · On-site

$25 - $35/hr

Temporary Position Work Type: Onsite Summary The QA Engineer is responsible for ensuring the timely ... Proficiency in Change Control, CAPA, Deviations, and Quality Systems documentation. * Understanding ...

Aerotek

Control Panel Technician

Largo, FL · On-site

$20 - $22/hr

Benefits are subject to change and may be subject to specific elections, plan, or program terms. If ... temporary role may include the following: • Medical, dental & vision • Critical Illness ...

Aerotek

Quality Control Inspector

Jacksonville, FL · On-site

$22 - $27/hr

Benefits are subject to change and may be subject to specific elections, plan, or program terms. If ... temporary role may include the following: • Medical, dental & vision • Critical Illness ...

AllSTEM Connections

Application Engineer

Orlando, FL · On-site

$87K - $153K/yr

Key Responsibilities Release Governance & Change Control • Change Record Management: Act as the ... For temporary assignments lasting 13 weeks or longer, AllSTEM Connections is pleased to offer major ...

BRPH

Construction Project Manager

Cape Canaveral, FL · On-site

Job requirements may include travel, temporary duty assignments, or relocations. Willingness to ... RFIs, change control and management, and any issues that may come upon the projects. SPECIALTY ...

Unicon Pharma Inc.

CQV Lead

Davie, FL · On-site

$45 - $50/hr

Monday - Friday 8.00AM to 5.00PM Temp to perm: Possible based on openings and performance Core ... change control, deviation investigations, and CAPA implementation. • Ensure alignment with cGMP ...

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Quality Assurance Engineer

Quality Assurance Engineer

TekWissen LLC

Tampa, FL • On-site

$25 - $35/hr

Temporary

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. 

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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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