Facilities Technician II (GMP) Wed - Sat, midnight to noon

UltraGenix Pharmaceutical
Bedford, MA; Woburn, MAPosted 14 March 2026

Job Description

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: ultra curious – Apply your biggest ideas in courageous ways The GMP Facilities Tech II performs preventative and corrective maintenance on a variety of complex utility systems within Ultragenyx GMP QC laboratory and manufacturing facilities. Equipment/systems include but is not limited to HVAC systems, cold storage, compressed air and gas systems, Reverse Osmosis (RO) and Water for Injection (WFI) systems, wastewater treatment, clean steam generation, fire detection/suppression, boilers, pumps/motors, etc. The Facilities Tech II will also perform corrective and preventive maintenance on GMP lab instruments and process equipment such as bioreactors, filling machines, centrifuges, rockers, chromatography columns, autoclaves, and glass washers. With minimal oversight, the Facilities Tech II must be able to interpret drawings, wiring diagrams, and equipment specifications to effectively perform troubleshooting and repair activities. 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. This is a 12 hour shift based position. Hours will be 12 midnight to 12 noon typically Wednesday through Saturday, but days could vary depending on coverage needed. Responsibilities: 1. Perform and document all corrective and preventative maintenance activities performed on GMP facility equipment and/or systems in accordance with GDP requirements. 2. Ensure GMP compliance with all facilities related activities including corrective and preventative maintenance. 3. Troubleshoot complex electrical and controls issues on all building systems and equipment. 4. Maintain all facility equipment and systems at optimum levels of performance, efficiency, and reliability. 5. Ensure that all facilities and maintenance activities are performed in accordance with current internal and external requirements for safety, quality, regulatory environmental, and compliance standards. 6. Execute continuous improvement projects to improve departmental performance. 7. Collaboratively work to resolve issues and improve equipment performance. 8. Always demonstrate good safety practices, including appropriate use of protective equipment. Reports and takes initiative to correct safety environmental hazards. 9. Respond to emergency service calls and resolve identified issues in a timely manner and in accordance with all safety, quality and compliance requirements. 10. Perform weekend walkthrough duties according to schedule. 11. Participate in an On-Call rotation for off hour facility emergencies. 12. Ensure that all required quality an ... (truncated, view full listing at source)
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