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Validation Engineer

  • ... Posted on: Sep 06, 2024
  • ... Stellent IT LLC
  • ... Venice, Florida
  • ... Salary: Not Available
  • ... Full-time
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Validation Engineer   

Job Title :

Validation Engineer

Job Type :

Full-time

Job Location :

Venice Florida United States

Remote :

No

Jobcon Logo Job Description :

Title: Validation Engineer
Location: Venice, Florida

  • 5 to 7 years of validation engineering experience with equipment, and / or facilities within a cGMP or FDA regulated environment
  • GMP/cGMP process experience.
  • Clear understanding of industry regulated guidelines for the validation of cGMP facilities
  • Relevant experience within the Pharmaceutical, or Biotechnology industries
  • Develop, write installation (IQ), operational (OQ) and performance qualification (PQ) protocols for production equipment, laboratories and process validation for production processes.
  • Coordinate execution of validation protocols
  • Analyze validation test data - determine systems or processes have met validation criteria.
  • Prepare validation or performance qualification protocols for manufacturing processes, systems, equipment for production.
  • Prepare summary reports for the completed qualifications including recommendations

    • Jobcon Logo Position Details

    Posted:

    Sep 06, 2024

    Employment:

    Full-time

    Salary:

    Not Available

    Snaprecruit ID:

    SD-CIE-0e53a163b85281326dd104e23230bfc77b3ca8ef4c75f0829f391e98f857a812

    City:

    Venice

    Job Origin:

    CIEPAL_ORGANIC_FEED

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    Title: Validation Engineer
    Location:     Venice, Florida

  • 5 to 7 years of validation engineering experience with equipment, and / or facilities within a cGMP or FDA regulated environment
  • GMP/cGMP process experience.
  • Clear understanding of industry regulated guidelines for the validation of cGMP facilities
  • Relevant experience within the Pharmaceutical, or Biotechnology industries
  • Develop, write installation (IQ), operational (OQ) and performance qualification (PQ) protocols for production equipment, laboratories and process validation for production processes.
  • Coordinate execution of validation protocols
  • Analyze validation test data - determine systems or processes have met validation criteria.
  • Prepare validation or performance qualification protocols for manufacturing processes, systems, equipment for production.
  • Prepare summary reports for the completed qualifications including recommendations

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