• Detroit, MI
    18 days ago

    Job Description

    Our client is seeking multiple Validation Engineers to support commissioning, qualification, and validation activities for a new manufacturing facility, including Process validation, cleaning validation and Computer system validation.

    • Bachelor's degree in Engineering, Life Sciences, Chemistry, Biotechnology, or a related field.
    • 3-7+ years of experience in validation within pharmaceutical, biotechnology, or medical device industries.
    • Experience in equipment qualification, process validation, or computer system validation (CSV).
    • Knowledge of GMP, FDA regulations, and applicable industry standards.
    • Experience preparing and executing IQ, OQ, and PQ protocols.
    • Proficiency in validation documentation, risk assessments, deviation investigations, and CAPA.
    • Familiarity with change control, SOPs, and quality management systems.
    • Strong technical writing, analytical, CAPA, and communication skills.
    • The consultant will be responsible for developing and executing qualification protocols, supporting SATs, and performing cleaning validation and CSV activities across a variety of process equipment and manufacturing systems.
    • Equipment may include filtration systems, filters, tanks, pumps, chromatography systems, bioreactors, and associated process equipment. Responsibilities will include preparing and executing IQ/OQ/PQ documentation as applicable, supporting equipment readiness and startup, reviewing technical documentation, and ensuring systems meet approved requirements and applicable GMP standards.
    • The ideal candidate will have a strong background in equipment qualification and validation within pharmaceutical, biotechnology, or other regulated manufacturing environments.
    • Experience with cleaning validation, computerized system validation, risk assessments, requirements traceability, deviation resolution, and validation documentation is highly desirable.
    • The consultant will work closely with engineering, quality, automation, and equipment vendors to resolve deficiencies, maintain compliance, and support the successful startup of manufacturing operations.

    Numbers & Facts

    LocationDetroit, MI

    Skills

    • Analysis Skillsunmatched
    • Automationunmatched
    • Biologyunmatched
    • Biotech and Pharmaceuticalunmatched
    • Change Controlunmatched
    • Chemistryunmatched
    • Chromatographic Systemsunmatched
    • Commissioning - Engineeringunmatched
    • Communication Skillsunmatched
    • Computer Systemsunmatched
    • Consultingunmatched
    • Corrective and Preventative Action (CAPA) Systemsunmatched
    • Documentationunmatched
    • Equipment Validationunmatched
    • FDA Requirementsunmatched
    • GMP (Good Manufacturing Practices)unmatched
    • Industry Standardsunmatched
    • Maintain Complianceunmatched
    • Manufacturingunmatched
    • Manufacturing Operationsunmatched
    • Manufacturing Systemsunmatched
    • Medical Equipmentunmatched
    • Process Manufacturingunmatched
    • Process Validationunmatched
    • Pumpsunmatched
    • Quality Managementunmatched
    • Requirements Managementunmatched
    • Risk Analysisunmatched
    • Standard Operating Procedures (SOP)unmatched
    • Startupunmatched
    • System Start-Upunmatched
    • System Validationunmatched
    • Technical Writingunmatched
    • Traceabilityunmatched
    • Validation Documentationunmatched
    • Writing Skillsunmatched

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