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Senior Utilities Plant Engineer II

Job in Bedford, Middlesex County, Massachusetts, 01730, USA
Listing for: Ultragenyx
Full Time position
Listed on 2025-11-15
Job specializations:
  • Engineering
    Process Engineer, Quality Engineering, Biomedical Engineer
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below

Why Join Us

Be a hero for our rare disease patients. At Ultragenyx, we fundamentally believe that taking real impactful action to care for the needs of patients and our people is always the right thing to do. Our vision is to lead the future of rare disease medicine by challenging the status quo and creating a new model that advances our field so more patients and caregivers can benefit from life‑changing treatments.

We do this by following the science, applying a novel rapid development approach, making innovative medicines at fair and reasonable prices, and creating a collaborative ecosystem to reach patients in meaningful ways.

Our commitment and care for patients extends to our people, so culture is an essential cornerstone for Ultragenyx. We remain continuously focused on creating a supportive and inclusive environment of profound learning and growth so employees can thrive in all areas of their lives, in and outside of work.

Position Summary

The Senior Utilities & Plant Engineer will partner closely with GMP Facilities and provide engineering support for GMP and non‑GMP utility systems (including WFI, HVAC, chilled water, electrical systems, condensate systems and gases) at Ultragenyx Gene Therapy GMP Manufacturing and Laboratory facilities in Bedford, MA and Woburn, MA. The candidate will be the primary engineering resource for operational support and process improvements related to the facility and utility systems.

Work

Model

Core Lab & Ops:
This role typically requires that the majority of the work be conducted on‑site and thus will be subject to certain on‑site safety protocols during the pandemic.

Responsibilities
  • Technical and Quality ownership of facility and utility systems including on‑site troubleshooting and investigations; provides on‑call operational support in the event of any equipment issues.
  • Develops preventative maintenance program and strategies within the CMMS that maximize system/equipment reliability and availability.
  • Use reliability‑centered maintenance concepts and data to prioritize efforts and system improvements/optimization. Monitor and trend repeat equipment failures and perform root‑cause analysis to identify cause and recommend and implement corrective actions, as necessary.
  • Help establish, monitor, and drive continuous improvements for facility and utility KPI’s.
  • Independently owns tasks and deliverables for projects and will be main Engineering point of contact for facility and utility projects from design through commissioning/validation.
  • Provide technical ownership of multiple complex projects/changes at a time.
  • Active training and mentoring of junior team members.
  • Solutions are expected to incorporate broad experience and input from expert & industry sources.
  • Subject matter expert for investigations of any facilities or equipment system deviations or failures and drives the development and implementation of CAPAs.
  • Owns and executes change management for facility and utility systems.
  • Ensure systems/equipment comply with industry standards and regulations.
  • Support the development and revision of governing system/equipment SOPs.
  • Identify and drive opportunities for innovation and efficiency in facility systems.
  • Supports equipment shutdowns and general repairs when necessary.
Requirements
  • Minimum of a Bachelor of Science degree in Chemical, Mechanical, or related engineering field preferred.
  • Minimum of 15 years of experience in a biotech engineering/manufacturing environment preferred.
  • Minimum of 15 years of experience in technical functions including Utilities/Plant Engineering, or related functions.
  • Demonstrated leadership skills in executing projects within an FDA/EMA regulated environment, including direct experience working at a biologic or advanced therapy medicinal product (ATMP) manufacturing site.
  • Experience and knowledge related to reviewing and approving equipment submittals, functional and configuration specifications, maintenance and calibration, equipment installation, and specifications with facilities, equipment, and utilities related to drug substance and/or drug product manufacturing.
  • Extensive knowledge of industry standards for cGMP engineering design,…
Position Requirements
10+ Years work experience
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