Validation Engineer II

Legacy Foundation-posted 15 days ago
Full-time • Mid Level
Onsite • Miami, FL
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The Validation Engineer II ensures the reliability, consistency, and compliance of our processes, equipment, and systems to meet regulatory requirements and quality standards. This role mainly drives the preparation and execution of validation documentation, including User Requirements Specifications, Installation, Operational and Performance Qualification Protocols and Validation Summary Reports. This includes leading and/or supporting validation of processes, equipment, and computer systems. The Validation Engineer II also provides assistance to system owners with impact risk assessments to identify the qualification and validation requirements, carrying out validation activities on equipment before returning or handing over to the system owner, and assist in arranging external services when required.

  • Perform critical review of Validation Engineer I project plans and related documents to ensure implementation is accurate and timely.
  • Independently lead and coordinate cross-functional projects and related resources to ensure completion in a timely manner. Communicate to management of performance against project plan.
  • Perform data and technical presentation reviews as needed.
  • Lead specific tasks or larger projects and ensure their successful completion, with minimal oversight.
  • Develop and execute validation plans for both new and existing processes, equipment, and systems.
  • Generate and execute qualification protocols to perform equipment qualifications and process validations. This includes establishing performance criteria, equipment troubleshooting, and ensuring compliance with safety and quality standards.
  • Support company's Master Validation Plan (MVP) including commissioning activities and protocols executions and establishing re-validation criteria.
  • Collaborate with cross-functional teams to provide validation-related guidance, solve technical problems, and contribute to project milestones.
  • Assess the impact of process, material, or equipment changes on validation status and provide guidance on revalidation or change control measures.
  • Identify potential risks associated with manufacturing processes and implement appropriate mitigation measures to minimize those risks effectively.
  • Train personnel involved in validation activities and offer expertise and support to other departments on validation-related matters.
  • Ensure personal and company compliance with all federal, state, company and regulatory bodies' regulations, policies, and procedures.
  • Other duties as assigned.
  • Bachelor's degree in engineering or a related technical discipline (e.g. Biology, Chemistry, etc.). Proficiency in microbiology preferred.
  • At least 2-5 years of experience in related Engineering role. Experience in validations preferred.
  • Strong knowledge of FDA, AATB, and cGTP guidelines preferred.
  • Experience in Tissue Banking, Pharmaceutical, Medical Device, or Biologics industry.
  • Experience with Non-Conformance, Deviation, Complaint, and Corrective and Preventive Actions (CAPAs) preferred.
  • Strong knowledge of relevant software applications (Microsoft Project, Word, Excel, and PowerPoint).
  • Effective oral, written, communication, and presentation skills.
  • Strong analytical and problem-solving skills.
  • Project management skills preferred.
  • Ability to be assertive and influence others and lead significant change.
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