Sr 2 Automation Engineer

USA - 3383 Shire Human Genetic Therapies, Inc.; Lexington (MA); On-site; USD 116,000 - 182,000; Full time

Job summary

Takeda in Lexington, MA seeks a Senior II Automation Engineer to lead control systems (DeltaV, PLC, DCS) in a regulated biopharma environment. You will balance hands-on support with ownership of engineering projects and guide automation strategy across the site.

You will define project scope, ensure high-quality delivery, support audits, develop SOPs and data standards, and collaborate cross-functionally with manufacturing, engineering, and site leadership to drive continuous improvement and

Qualifications

• Bachelor’s or Master’s degree in Chemical Engineering, Electrical Engineering, Computer Science, or related field.
• 8+ years of experience in industrial automation or control systems engineering.
• Strong expertise with DeltaV or similar DCS platforms and PLC programming.
• Experience in cGMP, pharmaceutical, biotechnology, or other regulated environments.
• Knowledge of ISA-S88/ISA-S95 standards and batch or continuous manufacturing processes.
• Knowledge of industrial control systems, instrumentation, and networking (Ethernet/IP, Profibus).
• Experience with data historians, reporting systems, and integration tools (OPC, SCADA).
• Demonstrated ability to lead complex projects and deliver solutions aligned with business goals.
• Familiarity with system validation, commissioning, and qualification processes.
• Strong problem-solving, communication, and cross-functional collaboration skills.

Responsibilities

• Serve as the primary SME for control systems (PLC, DCS, MES, and data systems).
• Support manufacturing operations by troubleshooting issues and ensuring system reliability and compliance.
• Lead the full project lifecycle from design through implementation for automation initiatives.
• Define project scope, strategy, and requirements while ensuring timely delivery of solutions.
• Oversee and review technical outputs of automation engineering work.
• Drive continuous improvement, system performance optimization, and innovation initiatives.
• Collaborate cross-functionally through daily operational and project meetings.
• Support audits, inspections, and compliance by preparing and presenting required data.
• Develop and maintain SOPs, work instructions, and engineering standards for automation programs.
• Ensure accurate documentation and lifecycle management of system specifications, drawings, and data.

Skills

Project leadership

Cross-functional collaboration

Communication

Problem-solving

Education

Bachelor’s or Master’s degree in Chemical Engineering, Electrical Engineering, Computer Science, or related field

Tools

DeltaV

DCS/PLC programming

SCADA

OPC

Job description

Job Description

About the Role: As the Senior II Automation Engineer, you will serve as a key automation leader within a high-impact manufacturing environment, supporting critical control systems that enable reliable and compliant biopharmaceutical operations. You will partner closely with manufacturing, engineering, and site leadership to ensure system performance, drive continuous improvement, and deliver innovative automation solutions. In this role, you will balance hands‑on operational support with ownership of complex engineering projects. You will also act as a trusted subject matter expert, guiding best practices and shaping automation strategy across the site. You will report into the Automation Lead.

How You Will Contribute

• Serve as the primary subject matter expert for control systems (PLC, DCS, MES, and ancillary data systems)
• Support manufacturing operations by troubleshooting issues and ensuring system reliability and compliance
• Lead the full project lifecycle from design through implementation for small to large‑scale automation initiatives
• Define project scope, strategy, and requirements while ensuring high‑quality, timely delivery of solutions
• Oversee and review technical outputs of automation engineering work
• Drive continuous improvement, system performance optimization, and innovation initiatives
• Collaborate cross‑functionally through daily operational and project meetings
• Support audits, inspections, and compliance activities by preparing and presenting required data
• Develop and maintain SOPs, work instructions, and engineering standards for automation programs
• Ensure accurate documentation and lifecycle management of system specifications, drawings, and data

Skills and Qualifications

• Bachelor’s or Master’s degree in Chemical Engineering, Electrical Engineering, Computer Science, or a related field
• 8+ years of experience in industrial automation or control systems engineering
• Strong expertise with DeltaV or similar DCS platforms and PLC programming
• Experience in cGMP, pharmaceutical, biotechnology, or other regulated environments
• Knowledge of ISA‑S88/ISA‑S95 standards and batch or continuous manufacturing processes
• Solid understanding of industrial control systems, instrumentation, and networking (e.g., Ethernet/IP, Profibus)
• Experience with data historians, reporting systems, and integration tools (e.g., OPC, SCADA platforms)
• Demonstrated ability to lead complex projects and deliver solutions aligned with business goals
• Familiarity with system validation, commissioning, and qualification processes
• Strong problem‑solving, communication, and cross‑functional collaboration skills

Takeda Compensation and Benefits Summary

We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.

For Location: USA - MA - Lexington - BIO OPS U.S. Base Salary Range: $116,000.00 - $182,270.00

The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.

EEO Statement

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.

Takeda is an equal opportunity employer.

Locations

USA - MA - Lexington - BIO OPS

Worker Type

Employee Worker Sub-Type Regular Time Type Full time Job Exempt Yes

Legal Notice

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Company Overview

Takeda is an industry-leading, global pharmaceutical company with an unwavering dedication to putting patients at the center of everything we do. We live our values of Takeda-ism – Integrity, Fairness, Honesty, and Perseverance – and are united by our mission to strive towards Better Health and a Brighter Future for people worldwide through leading innovation in medicine. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. At Takeda, you will make an impact on people’s lives – including your own.