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
• Assist with troubleshooting, optimization, and lifecycle support of process automation systems
• 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
• 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
• 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
• Experience working with industrial protocols including HART, Ethernet I/P, OPC and classic IO
• 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

Benefits

Competitive healthcare, plus voluntary benefit programs to support your unique needs
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

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.

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.