Quality Assurance Engineer

Job Description:

Are you a hardworking and dedicated QA Engineering professional located in Tampa, FL? Do you have experience in a Pharmaceutical Manufacturing environment?

Apply today to join a team where your growth, well-being, and success are our top priority!

Details:

• $35 - $40.99 per hour pay rate
• Full Time
• Contract - 1 year
• Onsite in Tampa FL
  
  

What's in it for you?

• Health, Dental, Vision insurance offered
• 401k options
• Work with a great team!
  
  

Only considering candidates with the following:

• Bachelor's degree in Engineering, Life Sciences, Chemistry, Microbiology, or related field (advanced degree preferred)
• Knowledge of Quality Assurance, Validation, and GMP-regulated manufacturing
• Understanding of cGMP regulations (FDA, EMA, ICH) and validation requirements
• Experience with IQ, OQ, PQ, PPQ protocols, and validation documentation
• Familiarity with commissioning and qualification of equipment, utilities, and lab systems
• Knowledge of computerized system validation (CSV) and data integrity requirements
• Experience with change control, CAPA, deviations, and quality systems
• Participation in internal, client, or regulatory audits
• Ability to support risk management and investigations across the product lifecycle
• Collaboration with Manufacturing, Engineering, MSAT, QA/QC, and Packaging teams
• Strong technical writing, documentation review, and reporting skills
• Ability to manage multiple projects in a GMP environment
• Experience supporting facility start-up, expansion, or inspection readiness (preferred)
  
  

Responsibilities:

• Review and approve engineering and validation documentation, including IQ, OQ, PQ, PPQ, validation master plans, risk assessments, and periodic reviews
• Collaborate with plant and external engineering teams on new installations and systems to ensure cGMP-compliant documentation
• Support all phases of the Validation Life Cycle, including design, operation, improvements, and revalidation
• Represent QA in multi-disciplinary teams for facility builds and laboratory moves, including commissioning, validation, and computerized system validation
• Create, review, and approve SOPs, Change Control, CAPA, and other quality system documentation
• Provide Quality validation support across multiple internal and external functions to meet project requirements and regulatory standards
• Interface with Manufacturing, Packaging, Engineering, MSAT, PD, and QA/QC to resolve process issues and implement changes
• Identify, analyze, and manage risk throughout the product lifecycle using risk management tools
• Assist with investigations and reviews of deviations related to manufacturing equipment, utilities, automation, computer systems, validation, and laboratory instruments
• Support continuous quality system improvements, including GMP Validation and Change Control Programs
• Participate in internal, client, and regulatory audits
• Maintain a cGMP-compliant facility in a state of 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 as needed
• Perform other tasks as assigned by the Senior Manager of QA Operations
  
  

Click apply today!

Corestaff powered by Swipejobs is a Women Owned company and an Equal Opportunity Employer. We believe we are best equipped to support our candidates and clients when we really know them. That means understanding, respecting, and valuing diversity- unique styles, experiences, identities, abilities, ideas and opinions- while being inclusive of all people.

Please note that we are unable to sponsor applicants requiring work authorization or visas for the positions currently available. We kindly request that only candidates who already possess the legal right to work in the United States apply for consideration.

$35.00 - $40.99 / hr

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