Senior Engineer I, Automation

Moderna; Marlborough (MA); On-site; USD 121,600 - 194,500; Full time

Benefits offered by this job

Competitive healthcare

Well-being programs

Family planning benefits

Generous PTO

Savings and investments

Location-specific perks

Job summary

Moderna is seeking an Individual to support the implementation, optimization, and lifecycle management of process automation systems across Moderna’s Marlborough manufacturing network. This role will help deploy and continuously improve automation platforms across both new and existing facilities.

This position requires hands‑on experience with DeltaV DCS, PLCs, SCADA, MES, and data integrations, collaborating with Manufacturing, Facilities, MSAT, Quality, IT, and Process Engineering teams to

Qualifications

• Bachelor’s degree in Engineering, Computer Science, Chemical Engineering, Electrical Engineering, or related technical discipline.
• 5–8 years of experience in pharmaceutical or biotechnology.
• Knowledge of Industry 4.0 concepts, ISA‑95 and ISA‑88 standards.
• Strong experience with Emerson DeltaV DCS process control systems.

Responsibilities

• Support implementation and expansion of process automation capabilities across facilities.
• Develop, maintain, and improve DCS/SCADA/PLC systems and related tooling.
• Assist with troubleshooting, optimization, and lifecycle support of automation systems.
• Lead validation and commissioning activities (FAT/SAT) as required.

Skills

Pharma/biotech experience

ISA-95/ISA-88

RESTful APIs

System integrations

Troubleshooting

Cross-functional collaboration

Documentation

Education

Bachelor's degree in Engineering/CS/related

Tools

Emerson DeltaV DCS

Kepware

OPC servers

SCADA systems

VMware

Job description

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 position is based in Moderna’s Marlborough, MA offices. This role will help deploy and continuously improve automation platforms across both new and existing manufacturing facilities.

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

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, 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 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

• 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 $121,600.00 - $194,500.00.

We are an E‑Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.

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!

Accommodations

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 [e-mail].