Sr. Engineer, GxP Systems

Moderna

3d • $121,600 - $194,500 • Hybrid

About The Position

ModernaTX, Inc. seeks a Sr. Engineer, GxP Systems for its Norwood, Massachusetts location. This role involves the design, deployment, validation, and management of digital enterprise instrumentation systems. The engineer will collaborate with business analysts and software/automation engineers throughout the product lifecycle of digital quality enterprise and laboratory instrumentation systems, including specific systems like Chromeleon (CDS), LogiLab SDMS, and SoftMax Pro. A key responsibility is ensuring compliance with FDA 21 CFR Part 11, GAMP 5, and USP 1058 AIQ requirements. The position requires translating system requirements into appropriate digital lab system solutions, managing system change controls and validation, and ensuring successful validation and integration of systems into connected instrument pipelines, robotics, and AI initiatives. The role also includes supporting periodic system reviews, revalidation, and upgrades, and ensuring GMP compliance is integrated into system design and maintenance. Computer System Validation (CSV) activities, including protocol development, execution, and documentation, are essential. The engineer will also resolve production issues, enforce data integrity principles (ALCOA+), participate in audits, implement automated file transfer solutions, and author/review SOPs and other documentation. Facilitating deviation investigations and CAPAs, supporting GxP compliance issue resolution, assessing infrastructure needs, and ensuring alignment with network, cloud, cybersecurity, and database teams are also part of the role. The position involves enterprise system design, configuration, and deployment, focusing on multi-site operations and optimized performance. Identifying and implementing new digital solutions, including automation and AI, to drive continuous improvement, enhance efficiency, and strengthen compliance is expected. Participation in improvement initiatives like CAPA effectiveness reviews and risk assessments is also required.

Requirements

• Master’s degree, or foreign equivalent, in Engineering (any), Computer Science, or related field and 3 years of experience as a Validation Engineer, System Engineer, or related position supporting computer systems validation.
• Alternatively, a Bachelor’s degree, or foreign equivalent, in the specified fields and 5 years of progressive, post-baccalaureate experience.
• 3 years of experience must include: Computer System Validation using IQ/OQ/PQ protocols; Ensuring ALCOA+ data integrity & regulatory compliance; Assessing system requirements, configuring network & security settings, and maintaining system stability & compliance for enterprise systems & infrastructure; System issue troubleshooting for laboratory instruments and systems; GxP Systems Administration and Compliance; Risk Management & FMEA (failure modes and effects analysis); GxP Records Management; and Root Cause Analysis and CAPA management for GxP deviation investigations.

Responsibilities

• Design, deployment, validation and management for digital enterprise instrumentation systems.
• Collaborate with business analysts and software/automation engineers in the complete product lifecycle management of various digital quality enterprise and laboratory instrumentation systems including the Chromatography Data System (Chromeleon), Scientific Data Management System (LogiLab SDMS), and data acquisition and analysis software for microplate readers (SoftMax Pro).
• Ensure all validated laboratory systems comply with FDA 21 CFR Part 11, GAMP 5, and USP 1058 Analytical Instrument Qualification (AIQ) requirements.
• Translate system, equipment, and data integration requirements from digital and business teams for deployment into the appropriate digital lab system solution.
• Manage system change controls and configuration updates and validate changes, ensuring that laboratory systems comply with regulatory and industry best practices.
• Ensure successful validation and integration of key systems into the connected instrument pipeline, robotics/automation capabilities and artificial intelligence initiatives.
• Support periodic system reviews, revalidation efforts, and version upgrades to maintain the validated state and operational efficiency.
• Ensure good manufacturing practices (GMP) compliance is built into the design, delivery, and maintenance of all systems.
• Conduct Computer System Validation (CSV) activities by developing and executing SDLC qualification protocols and writing system configuration specifications, risk assessments, and administration procedures.
• Resolve production issues.
• Implement and enforce data integrity principles across laboratory systems, ensuring compliance with Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, Enduring, and Available (ALCOA+) guidelines.
• Participate in internal and external audits as digital quality expert for a portfolio of systems.
• Implement automated file transfer solutions to support seamless data movement and ensure data integrity, in alignment with evolving business needs.
• Author, review, and maintain Standard Operating Procedures (SOPs), Work Instructions, Change Control Documents, and Training Materials for all laboratory systems.
• Facilitate Deviations, Investigation, Corrective and Preventive Actions (CAPA) of laboratory system issues or non-conformities.
• Support resolving Good Practices (GxP) compliance issues through root cause analysis, remediation plans, and preventive measures.
• Assess server and database requirements and work cross-functionally with Network, Cloud, Cybersecurity, and Database teams to complete the enterprise system multi-site extension.
• Ensure infrastructure design aligns with system requirements, to support seamless connectivity and enterprise-wide accessibility.
• Enterprise System Design and Configuration and Deployment of Infrastructure, ensuring proper system architecture and optimized performance for multi-site operations.
• Identify and implement new digital solutions, including automation and artificial intelligence (AI), that drive continuous improvement, enhance laboratory efficiency, ensure data integrity, and strengthen compliance tracking.
• Participate in improvement initiatives such as CAPA effectiveness reviews, risk assessments, and process optimizations to support sustained operational excellence in a GxP environment.

Benefits

• Best-in-class healthcare coverage, plus voluntary benefit programs to support your unique needs
• A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
• Family planning benefits, including fertility, adoption, and surrogacy support
• Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
• Savings and investment opportunities to help you plan for the future
• Location-specific perks and extras
• Annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior