Quality Engineering Project Manager

Katalyst HealthCares & Life Sciences Inc

  • North Chicago, IL
  • 4 days ago

    Highlights

    Ensure timely completion of quality documentation within Electronic Document Management Systems (EDMS) and Laboratory Information Management Systems (LIMS), where applicable. Bachelor's degree in Engineering (Mechanical, Chemical, Biomedical, Industrial, Manufacturing, Electrical, or related discipline), Quality Engineering, or a related scientific field.

    Numbers & Facts

    LocationNorth Chicago, IL

    Description

    The Quality Engineering Project Manager oversees quality engineering within operations, leading a team to support manufacturing and compliance activities.

    • Quality engineering expertise
    • Validation and qualification
    • Risk management activities
    • cGMP knowledge
    • Statistical quality systems
    • Electronic document management
    • Laboratory information management
    • Physical and chemical characteristics
    • Bachelor's degree in Engineering (Mechanical, Chemical, Biomedical, Industrial, Manufacturing, Electrical, or related discipline), Quality Engineering, or a related scientific field.
    • Lead quality engineering activities to support manufacturing operations, product quality, and regulatory compliance.
    • Manage quality engineering projects from planning through execution, ensuring timelines, budgets, and quality objectives are achieved.
    • Develop, implement, and continuously improve Quality Management System (QMS) processes and procedures.
    • Oversee equipment, process, cleaning, and computer system validation activities, including IQ/OQ/PQ documentation.
    • Provide technical leadership for investigations involving deviations, non-conformances, out-of-specification (OOS) results, and customer complaints.
    • Drive root cause analysis using quality tools such as 5 Whys, Fishbone Diagrams, and Failure Mode and Effects Analysis (FMEA).
    • Lead and support CAPA (Corrective and Preventive Action) activities to ensure effective resolution and continuous improvement.
    • Perform quality risk assessments and implement risk mitigation strategies in accordance with regulatory requirements.
    • Collaborate with Manufacturing, Engineering, Validation, Regulatory Affairs, Supply Chain, and R&D teams to ensure product quality and process robustness.
    • Ensure compliance with FDA regulations, cGMP, ISO standards, and other applicable regulatory requirements.
    • Support internal, customer, and regulatory inspections and audits by preparing documentation and addressing audit observations.
    • Review and approve validation protocols, technical reports, engineering change requests, and quality documentation.
    • Analyze quality metrics and statistical data to identify trends and recommend process improvements.
    • Lead process improvement initiatives using Lean, Six Sigma, or other continuous improvement methodologies.
    • Ensure timely completion of quality documentation within Electronic Document Management Systems (EDMS) and Laboratory Information Management Systems (LIMS), where applicable.
    • Monitor project milestones, identify risks, and communicate project status to stakeholders and senior management.
    • Mentor and provide technical guidance to Quality Engineers and cross-functional team members.
    • Support supplier quality activities, including qualification, audits, and issue resolution when required.
    • Participate in new product introductions (NPI), technology transfers, and manufacturing scale-up activities.
    • Maintain compliance with company quality policies, safety procedures, and industry best practices.

    Similar Jobs

    See more jobs