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:
- Supporting utility equipment systems from cradle to grave
- Creating partnerships with other teams like Utilities, Manufacturing, Maintenance, and Engineering
- Identifying and executing improvements to equipment, including design, construction, commissioning, and validation work on capital and operational projects
- Managing small engineering projects with some direction, including working with other teams and providing direction to contractors
- Contributing to multi-function teams to implement change and improve engineering design, construction, commissioning, and validation processes
- Maintaining and updating Engineering documentation including drawings, URSs, specifications, change controls, and technical reports
- Ensuring GMP compliance efforts, including personal training, validation document development and execution, compliance workflow tracking, and regulatory audit support
What You'll Do
Provide Plant Engineering support to utility systems, including:
- Monitoring and analyzing system performance
- Investigating equipment failures
- Making operational enhancements
- Executing continuous improvement projects
- Supporting project execution for small OpEx projects
- Working with other Engineering team members to support larger Capital projects
- Executing startup, commissioning, and validation for new and modified facility systems
- Maintaining and updating Engineering documentation as applicable
- Supporting GMP compliance efforts, including personal training, validation document development and execution, compliance workflow tracking, and regulatory audit support
- Bachelor's degree in engineering and 2+ years of progressive engineering experience
- Strong organization, interpersonal, oral, and written communication skills for working across groups and with key stakeholders and management
- 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 willing to participate in an on-call rotation and [rarely] work rotating, or extended shifts as needed to support shutdowns and major projects
- Prefer GMP facility experience 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
Who You Are
You are an energetic and technical person interested in learning a wide range of Engineering systems in a diverse and collaborative environment. You have effective communication and collaboration skills for working cross-functionally to assure objectives are met. You are a problem solver.
Qualifications
Preferred Qualifications
Pay and Benefits
Base compensation range: $77,000.00 - $100,000.00. Benefits include medical, dental, vision, life insurance, fitness and wellness programs, disability insurance, paid vacation, shutdown time off, holidays, sick time, parental leave, retirement plans, and tuition reimbursement.