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RayzeBio in Indianapolis, IN, seeks a Facilities Maintenance Supervisor to lead 3–5 technicians, oversee preventive and corrective maintenance across HVAC, electrical, plumbing, and utilities, and coordinate with contractors to ensure GMP-compliant operations at the RayzeBio radiopharmaceutical site.
You will supervise daily work, ensure safety, training, and performance, and report KPIs to leadership while maintaining CMMS records and supporting new equipment turnover.
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/
We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.
Job Title: Facilities Maintenance Supervisor
Department: Facilities Engineering
Location: Indianapolis, IN
FLSA Status: Exempt
Reports To: Associate Director, Facilities Engineering
Direct Reports: 3–5 (Facilities Technicians)
The Facilities Maintenance Supervisor leads the day‑to‑day operation, maintenance, and upkeep of building systems and infrastructure at RayzeBio's radiopharmaceutical manufacturing site in Indianapolis. This role directly supervises a team of 3–5 Facilities Technicians, coordinating and prioritizing preventive and corrective maintenance activities across HVAC, electrical, plumbing, chilled water, compressed air, and emergency power systems in both cleanroom and non‑cleanroom environments. Acting as the primary point of contact for day‑to‑day contractor activity, the Supervisor manages vendor scheduling, work quality, and site access for calibration, repair, test and air balance (TAB), HEPA certification, and minor improvement projects, escalating larger capital or engineering initiatives to the Associate Director of Facilities Engineering. This position bridges hands‑on technical execution with first‑line people leadership, ensuring the technician team is deployed effectively, trained, and held accountable to safety, quality, and GMP standards, while keeping site leadership informed on maintenance performance, backlog, compliance status, and contractor‑related quality issues.
High school diploma or equivalent required; technical certification, trade school education, or an Associate's degree in a relevant field (electrical, mechanical, HVAC, or similar) preferred.
5+ years of hands‑on facilities maintenance experience, including at least 1–2 years in a lead or supervisory capacity, preferably within pharmaceutical, healthcare, biotech, or another regulated industry.
Experience reviewing and overseeing contractor‑performed TAB activities and HEPA certifications in cleanroom, controlled environment, pharmaceutical, healthcare, biotech, or other regulated facilities preferred.
Experience coordinating outside contractors or vendors for maintenance, calibration, or facility improvement work.
Familiarity with GMP, EHS, and NRC compliance standards; radiopharmaceutical or sterile/injectable environment experience is a plus.
Strong working knowledge of building systems including HVAC, electrical, plumbing, chilled water, compressed air, and emergency power.
Demonstrated ability to lead, train, and hold a small technical team accountable in a fast‑paced, regulated environment.
Effective vendor and contractor management skills, including scheduling, scope clarification, and quality verification.
Ability to evaluate TAB reports and HEPA certification documentation, identify unacceptable results or documentation gaps, and coordinate resolution with contractors, Quality, and Engineering stakeholders.
Proficient with CMMS platforms (e.g., BMRAM, Maximo, SAP) and comfortable maintaining accurate maintenance and calibration records.
Working knowledge of BAS/BMS systems and standard diagnostic tools (volt/ohm meters, current clamps, signal generators).
Strong organizational and prioritization skills, with the ability to balance hands‑on troubleshooting with supervisory and administrative duties.
Clear written and verbal communication skills, including the ability to report status and issues to site leadership.
High degree of personal accountability, safety mindset, and professional integrity.
Uses AI tools to enhance individual productivity and quality of work.
While performing the duties of this job, the employee is regularly required to stand, walk, climb ladders and stairs, bend, stoop, push, pull, and reach, and must be able to lift and/or move up to 50 pounds. Specific vision abilities required include close and distance vision. This position requires periodic work in a GMP cleanroom environment, including gowning, and occasional exposure to mechanical and utility spaces.
The noise level in the work environment is usually moderate to loud in mechanical and utility areas. The role operates across office, mechanical/utility, and GMP manufacturing environments, and may occasionally require response to after‑hours equipment alarms or facility issues.
Monday – Friday, 1st Shift; however, occasional overtime or on‑call coverage may be needed to support building upkeep and production operations.
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.
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.
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.
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 adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
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/
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