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/

Summary

RayzeBio is seeking a LIMS Specialist, reporting to the Associate Director of Quality Control. The position will be responsible for the continuing implementation and ongoing operation of the Veeva LIMS system in support of the laboratories at RayzeBio's Indianapolis manufacturing plant.  The implementation consists of three phases, of which the first phase is complete.  After all phases are complete, the LIMS Sr. Associate Scientist will be responsible for continued operation of the system.

The position will be on-site; located at RayzeBio's manufacturing plant, in Indianapolis, IN.

Job Responsibilities

Essential duties and responsibilities include the following.  Other duties may be assigned.

• Develop LIMS procedures for the laboratories and manufacturing, as needed; develop and maintain documentation for LIMS processes, user guides, and system validation.

• Maintain, configure, and troubleshoot the LIMS to support laboratory workflows and data integrity.

• Serve as the primary point of contact for LIMS-related issues in the laboratories and production, coordinating with IT and laboratory staff for timely resolution.

• Implement system updates, enhancements, and change controls in accordance with regulatory requirements (including, but not limited to, GxP, 21 CFR Part 11).

• Develop and Maintain the current studies and sample management protocols in the laboratory and continue to implement these protocols in LIMS per laboratory and quality requirements.

• Provide user training and support to laboratory personnel, ensuring effective and compliant use of the LIMS.

• Participate in audits and inspections, providing LIMS data and documentation as required.

• Collaborate with cross-functional teams to support new laboratory initiatives and system integrations.

• Ensure data security, user access management, and backup procedures are in place and effective.

• Support laboratory business continuity and disaster recovery planning as it relates to LIMS.

• Conduct hands-on training sessions (e.g., lunch-and-learns) to demonstrate system navigation, sample and test lookup, and day-to-day LIMS use for laboratory staff as needed.

• Solicit and synthesize user feedback across laboratory stakeholders (e.g., via surveys) to inform system configuration and improve usability and data integrity.

• Support review of process engineering decisions, including electronic signature and audit-trail/reason-for-change requirements, to ensure alignment with 21 CFR Part 11.

• Maintain working knowledge of the LIMS implementation roadmap and key project milestones to support planning, on-site vendor visits, and readiness activities.

Skills and Qualifications

• BS in Chemistry, Science, or relevant field with seven to ten years of experience in pharmaceutical or other cGMP experience. An advanced degree with less experience will be considered provided the LIMS experience requirement can be met.

• One to three years of experience with LIMS system, experience with Veeva LIMS strongly preferred. Experience with other modern LIMS systems preferred (i.e. Labware).

• Experience with injectable pharmaceuticals or radiopharmaceuticals is strongly preferred.

• Experience with HPLC, TLC, GC, Gamma Spec, and ICP preferred; or experience with microbiology lab equipment preferred.  Experience with laboratory instruments in some form is required.

• Multi-disciplined scientist with GMP experience.

• Highly motivated and organized professional with the ability to work independently or in a team environment.

• Experience with root cause techniques such as 6 M's, 5 Why's, fishbone, or similar preferred.

• Very personable with strong communication skills.

• Excellent professional ethics, integrity, and ability to maintain confidential information.

• Must be comfortable working in a controlled environment with ionizing radiation and able to lift 40 lbs.

• Comfortable coordinating on-site vendor visits and cross-functional milestone reviews as part of a phased system implementation.

• Uses AI tools to enhance individual productivity and quality of work

Work Environment

The noise level in the work environment is usually moderate.

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

#LI-Onsite

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

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 [email protected]. 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/

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 [email protected] 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.