Sr. Engineer I, Automation
- Employer
- Moderna, Inc.
- Location
- Marlborough, Massachusetts
- Posted date
- Sep 28, 2026
View more categories
- Discipline
- Engineering, Automation Engineer
- Required Education
- Bachelors Degree
- Position Type
- Full time
- Hotbed
- Genetown
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Job Details
The Role
Moderna is seeking an Individual to support the implementation, optimization, and lifecycle management of process automation systems supporting Individualized Neoantigen Therapies (INT) across Moderna’s manufacturing network.
This role will help deploy and continuously improve automation platforms across both new and existing manufacturing facilities. The engineer will collaborate with cross-functional teams to deliver scalable, compliant, and integrated automation solutions that advance Moderna’s smart manufacturing initiatives and vision for lights-out manufacturing.
The ideal candidate is a hands-on, proactive automation engineer with strong technical expertise, a collaborative mindset, and a passion for learning and implementing new technologies in a fast-paced manufacturing environment.
This position is based in Moderna’s Marlborough, MA offices.
Here’s What You’ll Do
Automation Systems Implementation & Support
Support the implementation and expansion of process automation capabilities across new and existing manufacturing facilities
Support the development, maintenance, and improvement of DCS (DeltaV), PLCs (AB/B&R), SCADA systems, DHS (AVEVA PI), Robotics, VMware, including adoption of new technologies and future system upgrades
Assist with troubleshooting, optimization, and lifecycle support of process automation systems
Participate in commissioning, startup, FAT, SAT, and system deployment activities as required
Cross-Functional Collaboration
Collaborate with Manufacturing, Facilities, MSAT, Quality, IT Infrastructure, Process Engineering, and other cross-functional teams to define business and technical requirements
Support integration of automation systems with enterprise platforms including Operational Data Hub (ODH), Manufacturing Execution Systems (MES), VMware, and analytics environments
Standards, Platforms & Continuous Improvement
Contribute to the implementation and maintenance of plant floor Automation Design Guidelines and standards
Help standardize reusable automation aligned with ISA-95 and ISA-88 principles
Identify opportunities to improve processes, equipment, systems, and infrastructure through operational excellence initiatives and implementation of AI technologies.
Promote an AI/ML-forward mindset in system design and data utilization
Own Project Delivery & Lifecycle Management
Lead CAPEX projects from concept through commissioning and transition into OPEX
Provide ongoing lifecycle support for automation systems across Moderna facilities
Provide On-call and floor support
Validation & Compliance
Coordinate and support validation activities in collaboration with Manufacturing, Engineering, QA, and CQV teams
Support compliance activities related to cGMP, GAMP, CSV, and regulatory requirements
Develop and maintain automation documentation including URS, FRS, CDS, SOPs, and validation protocols
Support risk assessments, testing activities, and changing control processes
Here’s What You’ll Need (Basic Qualifications)
Bachelor’s degree in Engineering, Computer Science, Chemical Engineering, Electrical Engineering, or related technical discipline
Minimum of 5–8 years of experience in pharmaceutical or biotechnology.
Understanding of smart manufacturing and Industry 4.0 concepts, ISA-95 and ISA-88 industry standards
Strong experience in designing and supporting Emerson DeltaV DCS process control systems including continuous and batch processes.
Experience working with industrial protocols including HART, Ethernet I/P, OPC and classic IO.
Hands-on experience with middleware tools (e.g., Kepware, OPC servers)
Familiarity with PLCs, and SCADA systems, Robotics and VMware
Understanding of RESTful APIs and system integrations
Working knowledge of cGMP manufacturing operations and practices
Knowledge of GAMP, Computer System Validation (CSV), and regulatory compliance requirements
Background in CSV and regulatory compliance (21 CFR Part 11, Annex 11)
Experience developing automation documentation including URS, FRS, CDS, and validation protocols (IQ/OQ/PQ)
Strong troubleshooting and problem-solving skills in fast-paced manufacturing environments
Here’s What You’ll Bring to the Table (Preferred Qualifications)
Being proactive and self-motivated
Motivation to lead projects and drive initiatives to completion
Motivation and curiosity to learn new technologies and continuously improve
Creative, analytical, and strong problem-solving skills
Ability to work independently and make sound and timely decisions to achieve expected results
Ability to react under pressure to any given situation that may arise, in a professional manner and with positive results, in support of a multi-location environment
Ability to manage multiple priorities in a fast-paced environment
Collaborative mindset with a strong commitment to quality and operational excellence
A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative
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
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.
Our Working Model
As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. 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.
Equal Opportunities
Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law.Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!
Moderna is an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Accommodations
We’re focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations team at leavesandaccommodations@modernatx.com.
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Company
Moderna is advancing messenger RNA (mRNA) science to create a new class of transformative medicines for patients. Moderna’s platform builds on continuous advances in basic and applied mRNA science, delivery technology and manufacturing, providing the Company the capability to pursue in parallel a robust pipeline of new development candidates. Moderna is developing therapeutics and vaccines for infectious diseases, immuno-oncology, rare diseases and cardiovascular diseases, independently and with strategic collaborators.
mRNA is now a turning point in the history of science, medicine, technology, even humankind itself. With this breakthrough discovery, many of the world’s biggest and most challenging medical problems are no longer a question of “how?” but merely a question of “when?”
Come with us as we pursue the uncharted reaches of possibility and make your mark on the future of medicine.
Moderna employees share their thoughts on our culture, values and mission. To hear additional employee stories and learn more about our inclusive and innovative benefits offerings, visit us on our website.
Stock Symbol:
MRNA
Stock Exchange:
USNASDAQ GS
- Phone
- 617-714-6500
- Location
- 200 Technology Square
Cambridge, MA
