Sr Automation Controls Engineer - Indianapolis IN

VetJobs; Indianapolis (IN); On-site; USD 108,000 - 131,000; Full time

Job summary

RayzeBio in Indianapolis seeks a Senior Automation/Controls Engineer to lead automation systems for radiopharmaceutical manufacturing, report to engineering leadership, and support GMP manufacturing with deviation investigations, CAPA, and change control. On-site role with travel up to 15% and strong emphasis on safety and regulatory compliance.

The ideal candidate has 7+ years in automation/control engineering in regulated manufacturing, BS in a related field, and experience with

Qualifications

• BS degree in Electrical, Mechanical, Automation, or related Engineering field
• MS or advanced degree preferred
• Minimum 7 years' experience in automation/control engineering, ideally within the pharmaceutical or a regulated manufacturing industry

Responsibilities

• Ensure continuous operation and maintenance of automation and control systems for radiopharmaceutical manufacturing.
• Lead development, deployment, and lifecycle management of automation systems for radiopharmaceutical manufacturing processes and equipment.
• Support GMP manufacturing by leading deviation investigations, CAPA, and change control, with on-call after hours.
• Architect and implement PLC, HMI, SCADA platforms to enable facility expansions and commercialization.
• Oversee integration of automated systems with production lines and corporate business systems, ensuring GMP compliance.
• Optimize automation system performance, troubleshoot complex issues, and develop strategies for preventative and predictive maintenance.
• Provide technical leadership in commissioning, validation, and upgrades of process automation equipment.
• Collaborate with Engineering, Production, and Quality teams to define requirements and deliver high-quality automation solutions.
• Manage relationships with external vendors, partners, and contractors for system selection, installation, and validation.
• Author, review, and approve detailed technical documentation, including SOPs, system specifications, and validation protocols.
• Champion compliance with EHS, Radiation Safety, and regulatory requirements.
• Mentor and train junior engineers and staff on automation technologies.
• Leverage AI tools to enhance productivity and quality.
• Support business needs through up to 15% travel, as required.

Skills

Automation system architecture

PLC programming (Rockwell/Siemens)

SCADA

HMI development

Cognex vision systems

Robotics

Process equipment troubleshooting

Instrumentation and VFDs

Leadership

GMP/compliance knowledge

Education

BS degree in Electrical, Mechanical, Automation, or related Engineering field

MS or advanced degree preferred

Tools

Rockwell PLC

Siemens PLC

SCADA systems

HMI development tools

Cognex vision systems

Job description

Job Description

Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post.

The Senior Automation/Controls Engineer is an integral part of bringing RayzeBio’s innovative drug products to patients in need. In this role, you will report directly to engineering leadership and be primarily responsible for automation engineering work supporting clinical and commercial manufacturing objectives at the Indianapolis site(s).

Job Responsibilities

• Accountable for continuous operation and maintenance of automation and control systems for Radiopharmaceutical Clinical and Commercial manufacturing.
• Lead development, deployment, and lifecycle management of automation and control systems for radiopharmaceutical manufacturing processes and equipment.
• Support GMP manufacturing operations by leading and/or contributing to deviation investigations, CAPA development and execution, and change control activities, with on-call responsibility during evenings, weekends, and other non-standard business hours.
• Architect and implement robust PLC, HMI, SCADA, and related automation platforms to enable facility expansions and commercialization efforts.
• Oversee integration of automated systems with existing production lines and corporate business systems, ensuring regulatory and GMP compliance.
• Optimize automation system performance, troubleshoot complex issues, and develop strategies for preventative and predictive maintenance.
• Provide technical leadership and expertise in commissioning, validation, and upgrades of process automation equipment and instrumentation.
• Collaborate extensively with Engineering, Production, and Quality teams to define requirements and deliver high-quality automation solutions.
• Manage relationships and direct activities with external vendors, partners, and contractors for system selection, installation, and validation.
• Author, review, and approve detailed technical documentation, including SOPs, system specifications, and validation protocols.
• Champion compliance with EHS, Radiation Safety, and all relevant regulatory requirements, fostering a culture of safety and quality.
• Mentor and train junior engineers and staff on automation technologies and best practices.
• Leverage AI tools to enhance individual productivity and quality of work.
• Support business needs through up to 15% travel, as required.

Auto req ID 485278BR

Minimum Education Required Bachelors

Education and Experience

• Minimum 7 years' experience in automation/control engineering, ideally within the pharmaceutical or a regulated manufacturing industry.
• Experience in cGMP Biopharmaceutical, Radiopharmaceutical, or Medical Device environment equipment engineering design, development, and validation is preferred.
• BS degree in Electrical, Mechanical, Automation, or related Engineering field required.
• MS or advanced degree preferred.

Skills

• Expert in automation system architecture, design, integration, and troubleshooting.
• Strong knowledge of Rockwell/Siemens PLC programming, SCADA, and HMI development.
• Strong knowledge of Cognex vision systems and Robotics.
• Strong troubleshooting experience on process equipment, including but not limited to: Field instrumentation Control panels VFDs (Variable Frequency Drives).

Experience With Data Historian Systems And IT Infrastructure Preferred

• Deep understanding of GMP, validation, regulatory standards, and industry best practices.
• Proven leadership with the ability to lead complex technical projects and mentor team members.
• Commitment to continuous improvement and operational excellence.
• Excellent professional ethics, integrity, and ability to maintain confidential information.
• Organized and detail-oriented.
• Strong time management and organizational skills.
• Strong interpersonal communication skills.
• Motivated, adaptable, accountable, and collaborative. Able to support a manufacturing environment under pressure.

Physical Requirements

Standard office environment coupled with GMP production and facility environments.

Responsibilities also include the ability to lift 50 lbs., walk, bend, stoop, push, pull, reach, and climb stairs with or without accommodation.

Ability to sit or stand for long periods of time while performing duties.

Must be willing to wear personal protective equipment (PPE) as required.

Must be comfortable working with radioactive materials.

This is a position that requires working in a laboratory environment. Protective clothing, gloves, and safety glasses are required while working in a laboratory environment with radioactive materials.

Compensation Overview

Indianapolis - RayzeBio - IN: $107,904 - $130,754
The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully – carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance.

City Indianapolis

State Indiana

Job Category Health/Medical other

Job Code Pharmaceutical Pharmaceutical

Affiliate Sponsor Bristol Myers Sqibb BMS

Salary Range >$100,000