Associate Director, IT Digital Plant

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 youll 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 impacton our science on our teams and most importantly on patients. Learn more about RayzeBio: a Bristol Myers Squibb company is a dynamic biotechnology company headquartered in San Diego CA. The company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio is developing innovative drugs against targets of solid tumors. Led by a successful and experienced entrepreneurial team RayzeBio aims to be the global leader in radiopharmaceuticals.

Job Description

The Assoc. Director IT Digital Plant is an integral part of bringing RayzeBios innovative drug products to patients in this role you will report directly to the Exec. Director IT and be primarily responsible implementing RayzeBios vision for growth and leading efforts to enable digital processes to achieve commercialization objectives at newly developed site(s). The Indianapolis-based role will ensure the digital systems roadmap is enabled and maintained to successfully deliver novel Radiopharmaceutical technologies. You will work with lab & process automation large corporate systems small biotech systems across all functions for the new company site(s). Additional responsibilities will include setting and managing budgets and working with architectural and IT partners and specialty equipment manufacturers to achieve our technology and commercialization goals.

Job Responsibilities

Accountable for continuous operation and maintenance of IT lab & process automation systems (including MES LIMS local manufacturing quality control and quality management site IT systems) as well as associated site infrastructure.

Lead site service level management scope and process with IT groups and/or vendor managed services i.e. Service Level Agreements (SLAs) Disaster Recovery/Service Continuity etc.

Ensure Digital Roadmap leveraged and aligned to business outcomes. Drive for value realization.

Lead a group of indirect reports and service providers to deliver effective innovative and stable solutions that meet the needs of the site.

Active partner with the site functional leaders. Collaborate with site leadership to develop support and align strategies for business process improvements through information systems automation.

Provide IT leadership to site regulatory inspection readiness and data integrity initiatives.

Participate in high-level strategic communications with the business and site leadership teams.

Manage new demand from the various site functions (Manufacturing Operations Quality Supply Chain Manufacturing Science & Technology)

Identify key technology trends and how new technologies might be leveraged to provide better solutions to the manufacturing site

Responsible for the development of long-term (3 year) roadmaps identifying capabilities that have the greatest impact on business capabilities for the organization. Partnering and benchmarking with external sources.

Education and Experience:

• 10 years IT experience in a cGMP injectable or Radiopharmaceutical environment.

• Proven technical leadership and management experience.

• Demonstrated experience implementing automation and digitization projects.

• BS/MS Information Technology or similar degree or equivalent experience

Skills:

• Strong project management skills with a proven track record of leading multi-disciplinary teams in a regulated environment.

• Ability to influence stakeholders at all levels and drive strategic initiatives.

• Leads complex multi-disciplinary projects including resource and budget allocation and operational leadership.

• Oversees deliverable product sets vision and standards for work products challenges teams.

• It requires strong influence and trust resilience in difficult situations and the ability to encourage calm and rational behavior in teams.

• The leader identifies multiple solutions and recommendations for senior leaders structures communications to achieve organizational goals and tailors communication content and style for stakeholder understanding.

• The role also involves providing strategic feedback to vendors synthesizing multiple analyses to solve broader business issues and representing the discipline or function on program/project teams.

• Additionally the leader identifies gaps in capabilities ensures developmental opportunities for colleagues sets direction with little guidance contributes to multiple topic areas and drives functional direction.

Physical Requirements:

• Standard office environment coupled with GMP production and facility environment.

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

• Must be comfortable working in facility with radioactive materials.

If you come across a role that intrigues you but doesnt perfectly line up with your resume we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

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 employees 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 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 workplaceaccommodations/adjustmentsand ongoing support in their roles. Applicants can request a reasonable workplaceaccommodation/adjustmentprior to accepting a job offer. If you require reasonableaccommodations/adjustmentsin completing this application or in any part of the recruitment process direct your inquiries to. Visit 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: Protection

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