Job Details

Director of Reliability Engineering & Asset Management - BioPharma

JLL empowers you to shape a brighter way.

As the Director of Reliability Engineering & Asset Management in a BioPharma environment, you will lead and direct a team of professionals overseeing Reliability Engineering & Asset Management operations, maintenance, and strategic initiatives within pharmaceutical manufacturing and research facilities. This key leadership role involves managing and guiding subject matter experts within the following verticals: Facilities Engineering, Reliability Centered Maintenance, IIoT Smart Buildings, Special Projects, and BIM/VDC programs. You will be responsible for ensuring compliance with FDA regulations, cGMP standards, and other relevant industry requirements while fostering a culture of safety and operational excellence. Your mission will be to drive the adoption of new technologies and innovation, maintaining high performance in facility systems and operations. The primary vision is to develop and lead the best Reliability Engineering & Asset Management program within JLL, setting new standards in the BioPharma sector.

What your day-to-day will look like:

• Lead and oversee a team of SMEs and provide oversight for the following verticals:
  • Engineering programs
  • Strategic Reliability Engineering & Asset Management initiatives: Reliability Engineering & Asset Management operations - oversee, enhance, implement and lead CMMS systems, PMRM, PdM/CbM routes & inspections
  • Special projects, including budgets/timelines
  • BIM/VDC which includes energy & sustainability - IIoT Smart Buildings
  • Maintenance & operation of facility and process systems
  • Continuous improvement initiatives & within an outcomes-based model
• Oversee and support client building systems: HVAC, Electrical, Plumbing, Fire/life safety, Controls (BAS), Critical environments, Vertical Transportation, Building Envelope
• Collaborate with Quality, Manufacturing, and R&D teams
• Ensure infrastructure documentation, compliance and AHJ requirements are closely managed.
• Promote safety culture and embed within reliability and asset management programs, including bad actor reports and CAPA programs
• Coordinate with vendors and contractors as necessary
• Analyze maintenance and equipment data; develop KPIs and SLAs
• Plan work and personnel; ensure regulatory compliance
• Support quality management systems and documentation practices
• Act as primary Reliability Engineering & Asset Management liaison during inspections and audits

Required Qualifications:

• Bachelor's degree in Chemical, Mechanical, Electrical, or Biomedical Engineering; Master's preferred and or a minimum 10 years of experience in pharmaceutical/biotech engineering, with 5+ years in a leadership role within an engineering discipline.
• Strong command of FDA regulations, cGMP, and other relevant compliance standards.
• Certified Maintenance & Reliability Professional (CMRP) with a strong understanding and background implementing Reliability Centered Maintenance.
• CRL certification.
• 5S+Safety experience/knowledge.
• Strong understanding of ISO9000, 9001 & 9004 and ISO55000.
• Proven ability to manage large scale capital projects and engineering operations.
• Vendor and contract management experience.
• Experience with CMMS and preventive maintenance systems.
• Excellent leadership, analytical, and problem‑solving abilities.
• Exceptional communication and stakeholder management skills.
• Demonstrated ability to drive innovation and implement emerging JLL technologies in a regulated environment.

Preferred Qualifications:

• Strong leadership capabilities in leading a team of industry professionals.
• Strong capability of meeting and delivering key deadlines/milestones.
• Experience with aseptic processing, sterile manufacturing, and cleanroom design.
• Familiarity with process analytical technology (PAT), continuous manufacturing, and single use systems.
• Knowledge of automation systems and Industry 4.0 technologies in pharma.
• Proficiency in CAD/modelling software and project management methodologies (e.g., Six Sigma, Lean).
• Certification within a Six Sigma discipline, with a minimum of a Green Belt Certification.
• Familiarity with sustainability practices in pharmaceutical facility engineering.
• Advanced knowledge of MEP systems (mechanical, electrical, plumbing), including chilled water, steam, compressed air, and exhaust systems.
• Complete understanding of Asset Management governed under ISO55000.
• Familiarity with CAR & SAMP practices.

Estimated compensation for this position:

USD 174,900.00 – 214,200.00 per year

Location: Remote - San Diego, CA

Benefits:

• 401(k) plan with matching company contributions
• Comprehensive Medical, Dental & Vision Care
• Paid parental leave at 100% of salary
• Paid Time Off and Company Holidays