Validation Engineer

1 month ago


Philadelphia PA United States EPM Scientific Full time

We are looking for a detail-oriented Validation Engineer to join our client based in Philadelphia on a 12 months contract. You will be responsible for ensuring that manufacturing processes, equipment, and systems meet the required standards and regulations.


Key Responsibilities:

  • Develop and execute validation protocols (IQ, OQ, PQ) for equipment, processes, and systems.
  • Conduct risk assessments and develop mitigation strategies.
  • Ensure compliance with regulatory requirements (FDA, EMA, etc.).
  • Conducting regular inspections, performing calibrations, identifying areas for improvement, and alerting management of potential issues.
  • Collaborate with cross-functional teams to support validation activities.
  • Maintain accurate and detailed documentation of validation activities.
  • Investigate and resolve validation-related issues.
  • Participate in continuous improvement initiatives.



Required Qualifications:

  • Bachelor’s degree in Engineering, Life Sciences, or a related field.
  • Minimum of 5 years of experience in validation within the pharmaceutical industry.
  • Strong knowledge of regulatory requirements and guidelines.
  • Strong attention to detail and organizational skills.


Contract:

  • 40 hours per week
  • Start Date: ASAP
  • Contract Length: 12 months
  • Philadelphia, PA
  • W2 only

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