Engineer III, Facilities

About This Role

The Facilities Engineer supports both GMP and non-GMP utility systems at a dynamic biologics manufacturing site. Key responsibilities include creating partnerships with other teams, managing small engineering projects, and contributing to multi-function teams.

What You’ll Do

• Provide Plant Engineering support to utility systems, including monitoring and analysis, investigation of equipment failures, and execution of continuous improvement projects.
• Support project support and execution for small OpEx projects and larger Capital projects, including startup, commissioning, and validation.
• Maintain and update Engineering documentation, including drawings, URSs, specifications, change controls, and technical reports.
• Support GMP compliance efforts, including personal training, validation document development, compliance workflow tracking, and regulatory audit support.

Who You Are

• An energetic and technical person interested in learning a wide range of Engineering systems in a diverse and collaborative environment.
• Able to communicate effectively across groups and with key stakeholders and management.
• Able to follow standard practices, processes, and procedures; participate in key strategic initiatives; and identify potential improvements for utility and facility systems.
• A problem solver with strong organizational, interpersonal, oral, and written communication skills.

Qualifications

• Bachelor’s degree in engineering and 2+ years of progressive engineering experience.
• Strong organization, interpersonal, oral, and written communication skills.
• Experience with Engineering documentation requirements (drawings, specifications, URS/FRS, validation protocol, change management, etc).
• Experience with structured problem solving or related approaches.
• Ability to work 100% on site and participate in an on-call rotation and [rarely] work rotating, or extended shifts as needed to support shutdowns and major projects.

Preferred Qualifications

• Experience with GMP facility systems including documentation requirements for GMP manufacturing facilities such as Change Control and Validation.
• Engineering experience supporting clean utilities (air, gases, water), boilers, chillers, process glycol and tower/chilled water systems.
• Experience writing deviations and conducting investigations.