Facilities Maintenance Supervisor

The Facilities Maintenance Supervisor leads the day-to-day operation maintenance and upkeep of building systems and infrastructure at RayzeBios radiopharmaceutical manufacturing site in Indianapolis. This role directly supervises a team of 35 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.

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

• Directly supervise schedule and coach a team of 35 Facilities Technicians assigning daily work reviewing performance and supporting hiring onboarding and development.
• Plan and prioritize preventive and corrective maintenance work orders across HVAC electrical plumbing chilled water compressed air backup generator UPS and lighting systems to minimize downtime and ensure continuity of operations.
• Serve as the primary day-to-day site contact for contractors and vendors performing maintenance calibration and minor improvement work coordinating scheduling site access and scope confirmation and verifying work quality and completion.
• Review and supervise contractors performing test and air balance (TAB) activities and HEPA certification work ensuring reports results and field execution meet site expectations GMP requirements and applicable cleanroom performance standards.
• Support quality event management for facilities-related issues by providing technical input leading or supporting change controls and contributing to CAPA and deviation investigations and responses.
• Own and maintain the site CMMS work order queue for the maintenance team ensuring accurate timely closure of work orders and up-to-date equipment and calibration records.
• Conduct and oversee routine facility walkthroughs and inspections identifying safety performance or compliance issues and driving timely resolution.
• Monitor critical utility systems and respond to or direct the teams response to equipment alarms and facility issues including after-hours and on-call escalations as needed.
• Ensure maintenance activities are performed in compliance with GMP NRC and EHS requirements and support internal and external inspections as a subject matter resource for maintenance operations.
• Support commissioning and turnover activities for new equipment and facility spaces coordinating technician and contractor involvement as needed.
• Track and report team KPIs including work order aging PM completion rate and contractor performance to the Associate Director of Facilities Engineering.
• Assist with authoring and revising SOPs work instructions and CMMS procedures related to maintenance activities.
• Manage minor maintenance and improvement project budgets and quotes escalating capital-scale needs to the Associate Director.
• Participate in safety initiatives emergency response planning and drills and promote a strong safety culture within the maintenance team.

• High school diploma or equivalent required; technical certification trade school education or an Associates degree in a relevant field (electrical mechanical HVAC or similar) preferred.
• 5 years of hands-on facilities maintenance experience including at least 12 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 doesnt 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 Years Day.

U.S.-based job seekers can explore full benefit offerings at 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 qualified applicants with arrest and conviction records pursuant to applicable laws in your area.

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