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Director, Automation Engineering

Job in Bedford, Middlesex County, Massachusetts, 01730, USA
Listing for: Ultragenyx Pharmaceutical Inc.
Full Time position
Listed on 2026-06-09
Job specializations:
  • Engineering
    Systems Engineer, Electrical Engineering, Automation Engineering
Salary/Wage Range or Industry Benchmark: 125000 - 150000 USD Yearly USD 125000.00 150000.00 YEAR
Job Description & How to Apply Below

Position Summary

ultra innovative - Tackle rare and dynamic challenges

Work Model

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

Responsibilities
  • Strategic Focus Areas:
    • Development of an Automation Roadmap that encourages continuous improvement through the identification and implementation of new ideas that positively impact a segment or area of the organization and its overall performance.
    • Evaluate new technologies for their application in GMP manufacturing facility.
    • Collaboratively work with IT and other internal and external partners to resolve issues and improve site performance.
  • This job requires a level of technical proficiency in multiple skill areas and the ability to interpret complex information to solve problems. It also requires a service provider mindset that supports a variety of customers within Manufacturing, Engineering, Validation, QC, etc.
  • Works independently to drive all automation strategies and deliverables with limited to no direct supervision or technical oversight required. Represents automation systems and programs to worldwide regulatory agencies.
  • Ability to present to and solicit alignment from senior leadership on both known and unknown challenges/problems.
  • Provide technical solutions to a wide range of process, building, and networking challenges associated with automated systems.
  • Subject matter expert in all site automation systems.
  • Program, configure, and integrate equipment into the site OT Network, QMAS, and BMS systems.
  • Develop, review, and approve engineering documentation including equipment specifications, test protocols, engineering standards, and procedures.
  • Support the Manufacturing facility and QC Laboratory with regards to automation and instrumentation requirements.
  • Participate in cross‑functional teams created to perform investigations, root cause analysis, CAPA creation or improvement opportunities as needed.
  • Ensure that all required training is completed on time and current.
  • Manages employees and contract staff.
  • Manages contracts/SOWs, purchase orders, budgets for automation support & initiatives.
  • Establishes operational objectives and work plans and reviews objectives to determine success of the Automation Engineering department.
  • Participates with other senior managers to establish plans and objectives and make decisions on operational matters.
  • Requirements
  • Required education:
    Bachelor’s degree in chemical, Electrical, Mechanical, Biomedical Engineering, or Computer Science with appropriate industrial controls experience.
  • 10+ years of experience in manufacturing support environment, as a system integrator or automation engineer. 5+ years of Management experience preferred.
  • PLC and DCS coding, installation, and support, including but not limited to Allen Bradley, Siemens, and Delta

    V.
  • Understanding and configuration of systems such as PI, Win-911, and Info Batch.
  • Experience with BMS systems (Delta Controls preferred).
  • Experience with analytical equipment such as balances, pH/DO meters, Nova FLEX2, Beckman Coulter Vi-CELL, filter integrity testers, etc.
  • Understanding of instrumentation, electrical, and wiring standards.
  • Understanding of network architecture, including firewall, and switch configuration and virtualized environments.
  • Familiarity with industry standard communication protocols such as Ethernet IP, PROFINET, Modbus TCP, OPC, and BACnet.
  • Experience with current trends in automation and instrumentation to be able to select and implement modern controls architectures.
  • Adherence to domestic and international GMP regulations.
  • Experience with data integrity, specifically the understanding of FDA Part 11 and European Annex 11 requirements and experience applying these standards to the qualification of automation systems.
  • Able to effectively manage the automation lifecycle of controls components.
  • Familiarity with bioprocessing systems for Drug Substance and Drug Product manufacturing.
  • Physical Demand Requirements Manufacturing

    Facilities Mechanic:

    • 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 50 lbs.
    • Work in a…
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