Senior Engineer I, Automation

About 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.

Responsibilities

• 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
• Aid with troubleshooting, optimization, and lifecycle support of process automation systems
• Participate in commissioning, startup, FAT, SAT, and system deployment activities as required
• 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
• 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

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
• Familiarity with PLCs, and SCADA systems, Robotics and VMware
• 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

Preferred Qualifications

• 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

The salary range for this role is $121,600.00 - $194,500.00. 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.

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.