Moderna, Inc.

Senior Engineer, Data Historian and Analytics

Moderna, Inc. • $145K — $234K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor’s degree in Engineering, Computer Science, or related field
  • 5+ years of experience in information systems for biotech, pharmaceutical, or manufacturing
  • Familiarity with cGMP and manufacturing practices
  • Knowledge of ISA-95 standards
  • Understanding of computer systems validation (GAMP)
  • Proficient in XML, XSL, SQL, GraphQL
  • Experience with MQTT and OPC UA
  • Familiarity with OSIsoft PI System and Emerson DeltaV

Responsibilities

  • Lead project deliverables such as design documents and validation activities
  • Collaborate with stakeholders for global solutions
  • Ensure technical delivery of digital manufacturing data systems
  • Evaluate products and implement necessary enhancements
  • Support upgrade risk assessment and testing
  • Conduct user training sessions
  • Deliver software code enhancements and manage existing code
  • Diagnose and troubleshoot existing software issues
  • Mentor and train fellow engineers

Benefits

  • Competitive healthcare and voluntary benefit programs
  • Access to fitness, mindfulness, and mental health support
  • Family planning benefits including fertility and adoption support
  • Generous paid time off, including sabbatical and global recharge days
  • Savings and investment options for future planning
  • Location-specific perks and extras
Full Job Description

The Role


Moderna is seeking a Senior Engineer specializing in GMP manufacturing data historian and operational analytics systems to design, implement, support, and advance digital manufacturing data platforms across our manufacturing network.

This is a pharmaceuticalmanufacturing systems engineering role. The successful candidate will have hands-on experience with industrial data historians, manufacturing control-system integration, operational reporting and visualization, and the lifecycle management of computerized systems within a regulated GMP environment.


The Senior Engineer will provide technical ownership and engineering leadership for platforms such as the AVEVA/OSIsoft PI System, SIMCA analytical systems that collect and contextualize data from manufacturing equipment and automation platforms such as Emerson DeltaV.


The role will work closely with Manufacturing, Automation, Engineering, Quality, and Digital teams to ensure manufacturing data is reliable, contextualized, accessible, secure, and fit for GMP operational and analytical use.

This position is based in Norwood, MA.



Here’s What You’ll Do:


·         Serve as a technical subject matter expert for manufacturing data historian, operational analytics, visualization, and reporting systems supporting GMP manufacturing operations.

·         Design, configure, implement, validate, and maintain manufacturing data historian solutions, including historian data structures, asset models, calculations, interfaces, visualization, and reporting capabilities.

·         Provide technical ownership for AVEVA/OSIsoft PI System components and integrations, including PI Data Archive, Asset Framework, PI Vision, and historian interfaces/connectors, as applicable.

·         Provide technical ownership for SIMCA analytical systems to educate and drive user adoption with stakeholders and end users.

·         Develop and maintain integrations between manufacturing data systems and automation/control platforms such as Emerson DeltaV, using industrial communication technologies including OPC UA and MQTT.

·         Partner with Manufacturing, Automation, Process Engineering, MS&T, Quality, and other stakeholders to identify manufacturing data requirements and translate them into scalable technical solutions.

·         Assist in development and maintenance of SIMCA data models that contextualize process, equipment, batch, and manufacturing data for operational monitoring, troubleshooting, process understanding, reporting, and advanced analytics.

·         Design and support manufacturing dashboards, reports, calculations, and analytical applications using historian data and technologies such as Grafana, Tableau, Power BI, SIMCA, Informetric, or similar platforms.

·         Ensure manufacturing data integrity, availability, reliability, and appropriate contextualization across source systems, historian platforms, and downstream applications.

·         Troubleshoot historian, interface, data collection, reporting, and application issues and perform structured root-cause analysis.

·         Lead or support system lifecycle activities including architecture and design documentation, configuration, installation, testing, commissioning, validation, upgrades, periodic reviews, and retirement.

·         Apply GAMP, computer system validation, data integrity, and GMP requirements throughout the system lifecycle.

·         Perform system and application risk assessments and support validated change control, testing, and release activities.

·         Mentor and train fellow Engineers


Here’s What You’ll Need (Minimum Qualifications)


  • Bachelor’s Degree in Engineering, Computer Science, Information Systems, Automation, or a related technical or scientific field.
  • Minimum of 5 years of experience supporting manufacturing information, automation, historian, or operational technology systems within biotechnology, pharmaceutical, life sciences, or another regulated manufacturing environment.
  • Demonstrated hands-on experience implementing, configuring, supporting, or administering an industrial data historian, preferably AVEVA/OSIsoft PI System.
  • Experience working with manufacturing process and equipment data originating from DCS, PLC, SCADA, or other industrial automation systems.
  • Experience integrating manufacturing systems using technologies or protocols such as OPC UA, MQTT, SQL, XML, APIs, or similar industrial/data integration technologies.
  • Experience with Emerson DeltaV or comparable process-control platforms.
  • Working knowledge of GMP manufacturing operations, cGMP requirements, and regulated computerized systems.
  • Understanding of computer system validation and GAMP principles, including system lifecycle documentation, testing, change control, and risk-based validation.
  • Working knowledge of ISA-95 concepts and the integration of manufacturing systems across automation, operations management, and enterprise system layers.
  • Strong troubleshooting skills with the ability to diagnose data collection, connectivity, application, configuration, and system-performance issues.


 

Here’s What You’ll Bring to the Table (Preferred Qualifications)


  • Deep experience with the AVEVA/OSIsoft PI ecosystem, including PI Data Archive, PI Asset Framework, PI Vision, calculations/analytics, and PI interfaces or connectors.
  • Experience designing manufacturing historian architectures and data models for batch and continuous manufacturing environments.
  • Experience contextualizing historian data using equipment, process, batch, recipe, or ISA-95 manufacturing models.
  • Experience with manufacturing visualization and operational analytics tools such as Grafana, Tableau, Power BI, or equivalent platforms.
  • Experience with multivariate or process analytics platforms such as SIMCA.
  • Experience with manufacturing reporting platforms such as Informetric InfoBatch/InfoLog or comparable applications.
  • Experience integrating historian and analytics solutions with MES, LIMS, CMMS, ERP, or other manufacturing applications.
  • Understanding of data integrity expectations for regulated manufacturing systems, including principles associated with attributable, legible, contemporaneous, original, and accurate manufacturing data.
  • Experience developing SQL queries, calculations, scripts, or application configurations used to transform, contextualize, analyze, or present manufacturing data.
  • Experience working directly with Manufacturing, Automation, Engineering, MS&T, and Quality organizations to translate operational needs into technical requirements.
  • Experience supporting validated systems in a production environment, including incident management, change control, system upgrades, and lifecycle management.
  • Strong communication skills and the ability to work effectively in a global, matrixed organization.
  • A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.


Our Working Model


As we build our company, we have always believed that an in-person culture is critical to our success. This role is 100% onsite, reflecting the importance of being physically present to support the work, collaborate closely with colleagues, and contribute to our site-based operations.


Working onsite enables real-time collaboration, strong team connections, direct mentorship, and the hands-on partnership needed to deliver our mission. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact.


Moderna is a smoke-free, alcohol-free, and drug-free work environment.


Pay & Benefits

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

  • Competitive healthcare, 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 investments to help you plan for the future
  • Location-specific perks and extras

The salary range for this role is $145,900.00 - $234,200.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An individual’s position within the salary range will be based on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, experience, skills, performance, and business or organizational needs. 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.

About Moderna

Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.  


By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities. 


We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. 


If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. 

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