Sr. Facilities Engineer in Bedford

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. To achieve this goal, our vision is to lead the future of rare disease medicine. For us, this means going where other biopharma companies won’t go – 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 ways that are most meaningful for them.

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. Ultimately, we want to be an organization where we would be proud for our family, friends and children to work. If you want to have a meaningful impact, do the best work of your career, and grow a lot, both professionally and personally, come join our team.

Position Summary: ultrafocused – Work together to fearlessly uncover new possibilities. The Senior Facilities Engineer candidate will partner closely with GMP Facilities and be responsible for providing engineering support for GMP and non-GMP utility systems (including WFI, HVAC, chilled water, electrical systems, condensate systems, gases, etc.) at Ultragenyx Gene Therapy GMP Manufacturing and Laboratory facilities located 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 within the sites.

Work Model: Core Lab & Ops: This role typically requires that the majority of the work be conducted on-site.

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.
• Independently solves complex problems within area of expertise without supervision. Exercises independent judgment to determine and recommend appropriate actions on behalf of engineering and represents engineering programs to external regulatory agencies.
• Improves 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/optimisation. 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 8-10 years of experience in technical functions including Utilities/Plant Engineering, or related functions in a cGMP manufacturing environment.
• 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, commissioning, validation, and operation of bioprocessing equipment and utility systems related to drug substance and/or drug product manufacturing.
• Demonstrated experience working with Computerized Maintenance Management Systems (e.g., Blue Mountain RAM, Maximo, EAM, etc).
• Proven record with troubleshooting, problem solving, and investigational skills.
• Experience with quality systems including change controls, CAPAs, deviations, etc.
• Strong interpersonal and communications skills with ability to present to regulatory authorities, key stakeholders, and senior management effectively.
• Willingness to work in a dynamic and changing corporate environment. Flexible in the face of shifting needs and/or priorities.

Physical Demand Requirements:

• Stand for extended periods of time with periodic stooping/bending/kneeling.
• Ability to climb ladders and stairs of various heights.
• Able to lift, push, pull up to 50lbs.
• Work in a controlled environment requiring GxP gowning and wear protective clothing over the head, face, hands, feet, and body.
• Certain tasks may require use of a respirator; medical clearance will be required in advance.
• Working in temperature-controlled environments (cold rooms).

The typical annual salary range for this full-time position is listed below. This range reflects the characteristics of the job, such as required skills and qualifications and is based on the office location noted in this job posting. The range may also be adjusted based on applicant's geographic location. This position is eligible for annual bonus and equity incentives. Actual individual pay is determined by demonstrated experience and internal equity alignment.

Pay Range: $157,800 - $194,900 USD

Full Time employees across the globe enjoy a range of benefits, including, but not limited to:

• Generous vacation time and public holidays observed by the company
• Volunteer days
• Long term incentive and Employee stock purchase plans or equivalent offerings
• Employee wellbeing benefits
• Fitness reimbursement
• Tuition sponsoring
• Professional development plans

* Benefits vary by region and country

Ultragenyx Pharmaceutical is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital and veteran status, and any other status or classification protected by applicable federal, state, and/or local laws. Reasonable accommodation will be provided for all protected statuses or classifications protected by applicable law, including individuals with disabilities, disabled veterans, for pregnancy, childbirth, and related medical conditions, and based on sincerely held religious beliefs. Applicants can request an accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or in any part of the recruitment process, you may contact Talent Acquisition by emailing us at talentacquisition@ultragenyx.com.