Process Engineer III

Company : BioSpace, Inc.

Location : West Lebanon, NH, 03784

Posted Date : 15 September 2025

Job Type : Contractor

Category : Industrial Engineering

Occupation : Process Engineer

Job Details

Job Details
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. It's not your average production site - it's a tight-knit, supportive community working together to contribute to a better tomorrow for our patients. Ethics and quality are held in the highest regard, and a patient-focused mindset guides everything we do. We're looking for individuals who are self-starters with a strong work ethic to join our team. At Novo Nordisk, you will find opportunities, resources and mentorship to grow and build your career. Are you ready to realize your potential?
The Position
Responsible for the design and implementation of manufacturing processes, instrumentation, and equipment start-ups from the laboratory through manufacturing scale. This role will be part of a Manufacturing Engineering team providing direct support to the manufacturing floor with: equipment troubleshooting and direct support to manufacturing teams, conduct deviation investigations, root cause analysis, validations for new equipment installs, and other tasks helping our manufacturing operations succeed day to day. This role will work closely with different functional groups accross the site for projects including: Manufacturing, MSAT, QA, and other engineering teams.
This is an onsite based role 5 days a week Monday-Friday. Relocation assistance is available for eligible candidates. The specific level of this role will be commensurate with experience.
Relationships
Reports to: Lead Engineer, Manufacturing Engineering (Supervisor)
Essential Functions

Leads process and equipment troubleshooting to support deviations, corrective actions and related issues
Coordinate fabrication, procurement, installation, engineering start-up, and validation activities of new equipment and systems, including documentation of IQ/OQ protocols, test executions, and summary reports
Participate in the development and implementation of procedural or automation improvement changes
Participate 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
Point person for process improvement activities, including performing or authoring equipment specifications, user and functional requirements specifications, and necessary FAT and SAT protocols
Initiate and manage projects, tracking spending of budgets, creating scope of work, justification, risk assessments, cost estimates, implementing purchase order requisitions, and controlling

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