Lead Validation Engineer

Bristol Myers Squibb EU Policy; Indianapolis (IN); On-site; USD 124,000 - 151,000; Full time

Benefits offered by this job

Health Coverage

Paid Time Off

Job summary

RayzeBio in Indianapolis is seeking a Lead Validation Engineer to support GMP operations and to lead commissioning, qualification, and validation of facility, utility, equipment, analytical systems, and cleaning validation; you will help draft, review, and execute validation documentation to support the transition from construction to clinical development and commercial operations.

From a degree in engineering or science and 5+ years in radiopharmaceutical GMP manufacturing, you will apply

Qualifications

• BS or MS in a scientific or engineering discipline, or equivalent work experience.
• 5+ years in radiopharmaceutical, injectable, or other regulated GMP manufacturing.
• 5+ years of validation experience within GMP.
• Experience leading complex validation programs and cross-functional initiatives.
• Mentoring engineers or leading project workstreams preferred.

Responsibilities

• Lead cross-functional validation activities for facility, utility, equipment, analytical, cleaning, and process validation programs.
• Develop, implement, and continuously improve commissioning, qualification, and validation strategies for GMP and non-GMP spaces including office, warehouse, development, quality control, sterility/microbiology, and production areas.
• Partner with project teams, consultants, contractors, Quality, Engineering, QC, and Operations to deliver validation milestones aligned with business and compliance objectives.
• Provide technical leadership for day-to-day development and GMP manufacturing support, including troubleshooting, risk assessments, and validation impact assessments.
• Own and manage complex validation programs and ensure timely execution of protocols, reports, and lifecycle documentation.
• Review and approve validation documents including SOPs, forms, protocols, technical reports, deviations, CAPAs, change controls, and summary reports.
• Lead deviation investigations and support root cause analysis, corrective actions, and preventive actions related to validation and manufacturing systems.
• Drive continuous improvement projects that enhance compliance, efficiency, and operational readiness.
• Mentor, coach, and develop validation engineers and cross-functional team members.
• Support regulatory inspections and internal audits by presenting validation strategies, rationale, and supporting documentation.
• Track and communicate departmental KPIs, project status, risks, and resource needs to leadership.
• Support onboarding of new technologies, facility modifications, and expansion projects as required.

Skills

Technical writing

Regulatory knowledge

Leadership

Cross-functional collaboration

Communication

Project management

Validation expertise

AI in decision making

Independent work

Education

BS/MS in engineering or science

5+ years GMP experience

5+ years validation experience

Mentoring experience

Job description

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/

Summary

The Lead Validation Engineer will support the Radiopharmaceutical facility and GMP operations in Indianapolis and serve as a technical leader for commissioning, qualification, and validation activities. This role is responsible for leading the drafting, review, and execution of commissioning, qualification, and validation documents and protocols supporting highly specialized facility, utility, analytical, and process equipment. The position applies broad engineering and GMP knowledge to support the transition from construction to clinical development and commercial operations, while also providing leadership in process improvement, deviation investigation, CAPA management, new technology implementation, and future expansion initiatives.

Job Responsibilities

• Lead cross-functional validation activities for facility, utility, equipment, analytical, computerized systems, cleaning, and process validation programs.
• Develop, implement, and continuously improve commissioning, qualification, and validation strategies for GMP and non-GMP spaces including office, warehouse, development, quality control, sterility/microbiology, and production areas.
• Partner with project teams, consultants, contractors, Quality, Engineering, QC, and Operations to deliver validation milestones aligned with business and compliance objectives.
• Provide technical leadership for day-to-day development and GMP manufacturing support, including troubleshooting, risk assessments, and validation impact assessments.
• Own and manage complex validation programs and ensure timely execution of protocols, reports, and lifecycle documentation.
• Review and approve validation documents including SOPs, forms, protocols, technical reports, deviations, CAPAs, change controls, and summary reports.
• Lead deviation investigations and support root cause analysis, corrective actions, and preventive actions related to validation and manufacturing systems.
• Drive continuous improvement projects that enhance compliance, efficiency, and operational readiness.
• Mentor, coach, and develop validation engineers and cross-functional team members.
• Support regulatory inspections and internal audits by presenting validation strategies, rationale, and supporting documentation.
• Track and communicate departmental KPIs, project status, risks, and resource needs to leadership.
• Support onboarding of new technologies, facility modifications, and expansion projects as required.
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Education And Experience

• BS or MS in a scientific or engineering discipline, or equivalent work experience.
• 5+ years of experience in a radiopharmaceutical, injectable, or other regulated GMP manufacturing environment.
• 5+ years of validation experience within a GMP-regulated environment.
• Demonstrated experience leading complex validation programs and cross-functional initiatives.
• Prior experience mentoring engineers or leading project workstreams is strongly preferred.

Skills And Qualifications

• Strong technical writing and document review skills.
• Deep understanding of regulatory expectations for validation, lifecycle management, and risk management.
• Strong leadership, decision‑making, and problem‑solving skills.
• Ability to work independently while effectively influencing cross‑functional teams.
• Excellent communication, organization, and project management capabilities.
• Proven ability to prioritize multiple initiatives in a fast‑paced GMP environment.
• Broad validation knowledge across areas such as process validation, cleaning validation, computer system validation, equipment qualification, and QC assets.
• High level of professional ethics, integrity, and ability to maintain confidential information.
• Applies AI to improve team execution and decision‑making

Physical Demands

While performing the duties of this job, the employee is regularly required to sit, reach with hands and arms, and talk or hear. The employee must occasionally lift and/or move up to 30 pounds. Specific vision abilities required by this job include close vision and distance vision. This position requires working in a GMP cleanroom environment, wearing protective clothing, and handling radioactive materials.

Work Environment

The noise level in the work environment is usually moderate.

Compensation Overview:

Indianapolis - RayzeBio - IN: $124,449 - $150,803

The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.

Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.

Benefit Offerings Are Subject To The Terms And Conditions Of The Applicable Plans In Effect At The Time And May Require Enrollment. Our Benefits Include:

• Health Coverage: Medical, pharmacy, dental, and vision care.
• Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
• Financial Well‑being and Protection: 401(k) plan, short- and long‑term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.

Work-life Benefits Include:

Paid Time Off

• US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
• Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non‑Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays

Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

All global employees full and part‑time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.

• Eligibility Disclosure: The summer hours program is for United States (U.S.) office‑based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote‑by‑design or lab‑based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.

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 for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

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/

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 you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at [e-mail]. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response.

R1604504 : Lead Validation Engineer