Sr. Automation Controls Engineer

Bristol-Myers Squibb Company; Guam; Sur place; USD 108 000 - 131 000; Plein temps

Avantages offerts par ce poste

Wellbeing support

Retirement plan and financial security

Insurance offerings (medical, dental,視

Flexible Time Off

Holidays: 11 company holidays

Résumé du poste

RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, seeks a Senior Automation/Controls Engineer to support clinical and commercial manufacturing at Indianapolis sites. You will design, develop, and support automation and control systems for radiopharmaceutical processes, ensure GMP compliance, and mentor junior staff.

You will collaborate with engineering, production, and quality teams, lead deviation investigations, CAPA efforts, and work with external vendors to implement robust

Qualifications

• BS in Electrical, Mechanical, Automation, or related engineering field.
• MS or advanced degree preferred.
• 7+ years in automation/control engineering in pharma/regulated manufacturing.

Responsabilités

• Maintain and operate automation/control systems for radiopharmaceutical manufacturing.
• Lead development and lifecycle management of automation systems.
• Support GMP operations including deviation investigations, CAPA, and change control.
• Architect and implement PLC/SCADA/HMI platforms for expansion and manufacturing needs.
• Ensure regulatory and GMP compliance and mentor junior engineers.

Connaissances

Automation design

PLC programming (Rockwell/Siemens)

SCADA/HMI development

Cognex vision systems

Robotics

Process instrumentation

IT infrastructure knowledge

Leadership

Formation

BS in Electrical/Mechanical/Automation Engineering

MS preferred

Outils

Rockwell/Siemens PLCs

SCADA/HMI tools

Cognex vision

Robotics systems

Data historian systems

Description du poste

Life at BMS

At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact-on our science, on our teams, and most importantly, on patients. Learn more about RayzeBio: https://careers.bms.com/rayzebio/

Senior Automation/Controls Engineer

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).

You will design, develop, improve, manage, and support automation and control systems with novel Radiopharmaceutical technologies including, but not limited to, custom Hot Cells, formulation and filling lines, environmental monitoring systems, and building automation systems. Additional responsibilities will include working with engineering firms and specialty equipment manufacturers to achieve our clinical and commercial manufacturing objectives.

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.

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.

Benefits

• Subject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans - including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability).
• U.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year.
• Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays.
• Depending on eligibility, employees may also have access to additional time-off benefits, including paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs. Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Year's Day.
• U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits

RayzeBio and Bristol Myers Squibb

RayzeBio was acquired by Bristol Myers Squibb (BMS) in 2024 and is a wholly-owned subsidiary of BMS; however, RayzeBio will continue to operate as a standalone organization.

Supporting People with Disabilities

BMS and RayzeBio are dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [e-mail] . Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS and RayzeBio will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

For roles based in Los Angeles County only

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/

For roles based in Washington State only

If you live in or expect to work from Washington State if hired for this position, please visit this page for important information about the Washington Fair Chance Act.

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection .

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If this posting is missing required information required by local law or incorrect, contact BMS at [e-mail] with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.