Technician II, Engineering - Process

About the Department

At Novo Nordisk, we want to make a difference. For more than 100 years, we have led the way in diabetes care. Being part of Novo Nordisk allows our employees to embark on the opportunity to help improve the quality of life for millions of people around the world.

Our Bloomington, Indiana site is a state‑of‑the‑art facility where we have an integrated model from process and formulation to clinical and commercial biomanufacturing and drug product fill/finish and packaging. The Bloomington campus is a recognized facility where talented teams work with innovators to help develop, manufacture and supply products to patients around the world.

At Novo Nordisk, you will find opportunities, resources, and mentorship to help grow and build your career. Are you ready to realize your potential? Join Team Novo Nordisk and help us make what matters.

A Production Technician's primary duty is to provide direct technical support to operations area as it relates to equipment. This role will work collaboratively with multiple functions and departments to ensure equipment and associated production systems operate in a safe, and quality-oriented manner.

Responsibilities include:

providing training and assessment support for equipment operation, set‑up, changeover, and troubleshooting, providing recommendations and implementing solutions to resolve equipment and/or process problems in a timely manner, creating and revising GMP as it relates to equipment activities, supporting or owning work orders and preventative maintenance.

NOTE:

This role works 6PM - 6:30AM on a 2/2/3 rotating schedule (Shift

B)

Reports to Manager or Supervisor.

• Complete work under supervision by more experienced team members with increasing independence as experience, training, and job specific aptitude are gained
• Use judgment within generally defined guidelines to identify solutions to problems
• Interact with other departments to schedule activities around the production schedules of the cGMP Manufacturing and Process Development departments. Schedule self‑performed work assigned at beginning of month and due by end of month
• Follow general instructions on routine work and detailed instructions of new work
• May design new approaches to problems encountered and use a wide application of complex principles, theories, and concepts in the specific field
• Use hand tools, power tools, and delicate testing equipment in performance of duties
• Complete non‑routine repair work orders for regulated and unregulated systems
• Effectively document work performed following required documentation practices
• Be available and respond to site as part of the on‑call rotation (optional for Calibration)
• Escort and supervise contractors through facility for routine inspections or repairs, ensuring they complete activities per procedure or agreements
• Perform basic troubleshooting as it related to assigned job duties
• Work with shipping to send out equipment or standard for offsite vendor service and track status
• Contribute to the creation of maintenance and calibration procedures and update existing procedures to match best practices and lessons learned
• Identify and order spare or replacement parts for equipment utilizing inventory management system
• Recommend facility improvements to meet OSHA safety, ISPE, or FDA guidelines
• Opportunity to contribute on Safety Committee, Environmental Engagement Committee, or other corporate responsibility areas
• Assist with onboarding new equipment and retiring obsolete equipment
• Follow all safety and environmental requirements in the performance of duties
• Other duties as assigned

Freq…