Facilities Engineer; Junior - Senior Level); West Lebanon, NH

About the Department

Site New Hampshire, located in West Lebanon, is where Novo Nordisk’s life‑saving treatments are brought to life. Our manufacturing facility produces a global supply of our hemophilia and growth hormone product lines, as well as our next generation of cutting‑edge medications.

• Leading pay and annual performance bonus for all positions
• 36
  
  Paid days off including vacation, sick days & company holidays
• Health Insurance, Dental Insurance, Vision Insurance
• Guaranteed 8% 401K contribution plus individual company match option
• 14weeks Paid Parental Leave
• Free access to Novo Nordisk-marketed pharmaceutical products

At Novo Nordisk, you will find opportunities, resources and mentorship to grow and build your career. Are you ready to realize your potential?

Responsible for supporting the design and implementation of manufacturing support processes, instrumentation and equipment start‑ups for offices, labs and manufacturing scale. This role provides support for facilities processing, engineering, design, project coordination, start‑up and validation of GMP and non‑GMP utilities and facilities areas and systems. This role will primarily support our black utilities systems such as: chilled water, HVAC, plant steam, wastewater/water treatment, and electrical distribution.

This role will work cross functionally with departments across the site and work closely with project managers to support their ongoing projects. This is an onsite based role Monday‑Friday at our West Lebanon, NH bio‑production facility. Job title and level will be commensurate with experience. Prior experience in a GMP or similar cleanroom/sterile environment is a plus but not required.

Reports to:

Senior Manager, Project Engineering

• Facilities, Utility, Systems and Equipment (FUSE) troubleshooting to support deviations, corrective actions and related manufacturing impact or quality issues
• Tracking and evaluating process trends or issues in collaboration with quality, mfg. sciences and manufacturing
• Coordinating fabrication, procurement, installation, engineering start‑up and validation activities of new equipment and systems including documentation of IQ/OQ protocols, executions and summary reports
• Participate in the development and implementation of procedural or automation improvement changes
• Participating in design and hazard reviews of plant expansions or process changes and serving as the technical point of contact or user representative for contractor services including design, fabrication, installation and validation
• Serves as an interface between engineering, facilities, process development, quality assurance, validation and operations
• Technical point of contact for solvent, waste and emission control and related cost optimizations/efficiencies
• Point person for assigned process improvement activities. These may include performing or overseeing material and energy balances, creating/update Planviews, Isometrics, Orthographics, P&IDs and PFDs, authoring equipment specifications, user and functional requirements specifications and necessary FAT and SAT protocols
• Managing small projects and tracking spending of budgets, creating scope of work, risk assessments, justification, cost estimates, implementing purchase order requisitions, contracts, funding requests and controlling their payment
• Design and execution of engineering runs to test equipment or to troubleshoot problems
• Partner with contractors on troubleshooting assistance for issues found in the manufacturing environment
• Ability to provide evening, nighttime and weekend on‑call support as needed
• Incorporates the Novo Nordisk Way and 10 Essentials in all activities and interactions with others
• Performs all job…