Sr. Engineer, GxP Systems

Reposted 7 Days Ago
Be an Early Applicant
2 Locations
In-Office
122K-195K Annually
Senior level
Healthtech • Biotech
The Role
Design and manage validation and integration of digital enterprise systems. Collaborate on laboratory instrumentation systems, ensuring compliance and data integrity while conducting audits and resolving issues.
Summary Generated by Built In

JOB DESCRIPTION

Title:                    Sr. Engineer, GxP Systems

Reports to:        Director, Product Management

Function:            Digital

Location:            Norwood, MA

The Role:

ModernaTX, Inc. seeks a Sr. Engineer, GxP Systems for its Norwood, Massachusetts location.

Here’s What You’ll Do:

  • 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.

Here’s What You’ll Bring to the Table:

Minimum Requirements:

  • Requires a 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.

  • In the alternative, employer will accept a Bachelor’s degree, or foreign equivalent, in the specified fields and 5 years of the specified 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.

  • May telecommute up to 2 days per week.

The salary range for this role is $121,600 to $194,500. This range reflects the lowest to highest salary we, in good faith, believe we would pay for this role at the time of this posting. The minimum target pay for this particular position, based on its primary location, is $148,600 to $194,500. An individual’s placement within the range will depend on several factors, including but not limited to specific competencies, relevant education, qualifications, certifications, experience, skills, performance, and business or organizational needs.

Apply at https://modernatx.wd1.myworkdayjobs.com/en-US/M_tx (Job ID: R19156) or email resume and cover letter to [email protected] with subject line: R19156

Pay & Benefits

At Moderna, we believe that when you feel your best, you can do your best work.  That’s why our US benefits and global well-being resources are designed to support you—at work, at home, and everywhere in between.

  • 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

The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance.

#DNI

Pay & Benefits

At Moderna, we believe that when you feel your best, you can do your best work.  That’s why our US benefits and global well-being resources are designed to support you—at work, at home, and everywhere in between.

  • 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

The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance.

Skills Required

  • Requires a Master's degree, or foreign equivalent, in Engineering, Computer Science, or related field
  • 3 years of experience as a Validation Engineer, System Engineer, or related position supporting computer systems validation
  • 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
  • GxP Systems Administration and Compliance
  • Risk Management & FMEA
  • GxP Records Management
  • Root Cause Analysis and CAPA management for GxP deviation investigations

Moderna Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Moderna and has not been reviewed or approved by Moderna.

  • Fair & Transparent Compensation Pay is commonly characterized as fair, competitive, and a financial positive, with base pay complemented by bonus and other cash elements.
  • Equity Value & Accessibility Long-term rewards commonly include stock options and RSUs, positioning equity as a meaningful part of overall compensation rather than an occasional add-on.
  • Parental & Family Support Family-related support is extensive, including fully paid parental leave, paid family caregiver leave, family-building benefits such as fertility/adoption/surrogacy support, and childcare resources.

Moderna Insights

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The Company
Cambridge, Massachusetts
6,848 Employees
Year Founded: 2010

What We Do

At Moderna, we believe messenger RNA, or mRNA, is the “software of life.” Every cell in the body uses mRNA to provide real-time instructions to make the proteins necessary to drive all aspects of biology, including in human health and disease. Given its essential role, we believe mRNA could be used to create a new category of medicines with significant potential to improve the lives of patients. We are pioneering a new class of medicines made of messenger RNA, or mRNA. The potential implications of using mRNA as a drug are significant and far-reaching and could meaningfully improve how medicines are discovered, developed and manufactured. To learn more, visit www.modernatx.com. This Moderna page is not the appropriate place to report adverse events (side-effects) for any products. If you are or someone you know is experiencing a side effect, please reach out to your healthcare professional. Moderna is continuously monitoring the safety of its products. We encourage you to report any side effects directly to us at 1‑866‑MODERNA (1‑866‑663‑3762).

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