Senior GxP Instrument Systems Engineer

Pharmatek Consulting

  • Marlborough, Massachusetts
  • 30+ days ago
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    Skills

    • Artificial Intelligence (AI)unmatched
    • Automationunmatched
    • Automation Engineeringunmatched
    • Automation Systemsunmatched
    • Biologyunmatched
    • Biotech and Pharmaceuticalunmatched
    • Business Analysisunmatched
    • Change Controlunmatched
    • Change Managementunmatched
    • Chromatographic Systemsunmatched
    • Cloud Computingunmatched
    • Code of Federal Regulationsunmatched
    • Communication Skillsunmatched
    • Computer Scienceunmatched
    • Cross-Functionalunmatched
    • Data Qualityunmatched
    • Document Managementunmatched
    • External Auditunmatched
    • GMP (Good Manufacturing Practices)unmatched
    • GxPunmatched
    • Instrumentationunmatched
    • Internal Auditunmatched
    • Interpersonal Skillsunmatched
    • Laboratory Analysisunmatched
    • Laboratory Information Management System (LIMS)unmatched
    • Laboratory Managementunmatched
    • Laboratory Systemsunmatched
    • Maintain Complianceunmatched
    • Multitaskingunmatched
    • Process Improvementunmatched
    • Process Managementunmatched
    • Product Lifecycle Managementunmatched
    • Project Engineeringunmatched
    • Quality Controlunmatched
    • Quality Managementunmatched
    • Regulationsunmatched
    • Regulatory Complianceunmatched
    • Roboticsunmatched
    • Scientific Data Management System (SDMS)unmatched
    • Software Engineeringunmatched
    • Software as a Service (SaaS)unmatched
    • Standard Operating Procedures (SOP)unmatched
    • System Integration (SI)unmatched
    • Systems Engineeringunmatched
    • Systems Maintenanceunmatched
    • Team Playerunmatched

    Description

    For a Biotech Company We are looking for an Instruments Engineer:

    The qualified GxP Instrument Systems Engineer / Senior Project Engineer will be responsible for the design, deployment and management of automation and digital enterprise instrumentation systems that support Quality Control laboratories and system integration with connected Digital platforms.

    LOCATION

    On-site 3-4 days/week between Marlborough, MA 

    JOB RESPONSIBILITIES

    Collaborate with Business Analysts and Software/Automation Engineers in the complete product lifecycle management of Digital Quality Automation Systems (Hamilton Venus, Waters Andrew+ with OneLab, etc.) and Enterprise Instrumentation Systems (Chromeleon Chromatography Data System, Scientific Data Management System (LogiLab), CFR Gateway (LogiLab), SoftMax Pro, MODA, etc.) including optimizations, support, maintenance updates and version upgrades

    Translate system/equipment/data integration requirements from various teams into deployable Digital Laboratory System solutions

    Manage change control for regulatory Digital documentation (SOPs, work instructions, etc.) required to demonstrate appropriate compliance

    Partner with stakeholders to validate and integrate key systems into the connected instrument pipeline, future robotics/automation capabilities and AI initiatives

    Identify opportunities to optimize current processes and implement upgraded solutions

    Ensure GMP compliance in the design, delivery, and maintenance of all systems

    Maintain inspection readiness throughout the duration of the project

    Participate in internal and external audits as required



    Requirements

    Bachelor’s degree or equivalent in science, engineering, or computer science discipline

    5 to 7+ years’ experience designing, implementing, and managing life sciences enterprise systems (CDS, SDMS, LIMS, ELN, LES) in a bio pharmaceutical GMP environment

    Direct experience with automation solutions such as Hamilton Venus

    Experience working with advanced automated laboratory analytical systems such as Waters Andrew+, Oxford Nanopore, and Hamilton Venus liquid handlers

    Experience with GAMP and GxP compliance regulation

    Experience with data integrity regulations, instrument integration and laboratory digital workflow optimization

    Experience with Digital systems hosted in the cloud and an understanding of connectivity between on-prem systems and SAAS/Cloud

    Strong understanding of core laboratory systems, related processes, and quality management workflows

    Ability to work independently and in a team setting, with the ability to effectively communicate cross-functionally

    Ability to support multiple concurrent projects in a fast-paced environment

    Strong interpersonal and relationship-building skills



    Benefits

    Attractive Base Salary plus Benefits 


    No Sponsorship Available for this Role.

    Numbers & Facts

    LocationMarlborough, Massachusetts
    Websitewww.consultpharmatek.com

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