Operator , Inspection; WPM - F, S, S

Join to apply for the Operator I, Inspection (WPM - F, S, S) role at Bio Space

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.

• Leading pay and annual performance bonus for all positions
• All employees enjoy generous paid time off including 14 paid holidays
• Health Insurance, Dental Insurance, Vision Insurance – effective day one
• Guaranteed 8% 401K contribution plus individual company match option
• Family Focused Benefits including 14 weeks paid parental & 6 weeks paid family medical leave
• Free access to Novo Nordisk-marketed pharmaceutical products
• Tuition Assistance
• Life & Disability Insurance
• Employee Referral Awards

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.

Operate and Maintain Manual, visual inspection production process to achieve production goals.

Shift: WPM Fri - Sunday 6pm-7:30am

This will be the initial shift, but may change in the future due to business needs, so candidates must be flexible for shift changes, including working weekends.

Reports to Manufacturing Supervisor.

• Entry-level position with little or no prior relevant training or work experience
• Work is prescribed and completed with close supervision
• Duties are clearly defined, and methods and tasks are described in detail
• Safely operates basic equipment
• Supports cleaning and organizational efforts, including maintaining visual factory
• Required to read, understand, and follow GMP documents
• Participates in area continuous improvement activities
• Reports safety, quality concerns, and recommends improvements
• Demonstrates mathematical skills, including the ability to perform addition, subtraction, multiplication, division, and conversions
• Accurately count product via product count procedures
• Must be able to effectively palletize product and material per written specifications
• Inspection:
  Perform inspection techniques for manual visual inspection product families
• Perform inspection activities while sitting in a lighted booth for a 12-hour shift
• Perform inspection activities while operating in a Semi-Automated Syringe Inspection system and a Semi-Automated Vial Inspection System
• Perform inspection activities within a fully automated inspection process
• Packaging:
  Perform basic packaging activities by constructing secondary and tertiary containers for finished packaging products
• Must be able to stand for a 12-hour shift
• Must be able to perform manual packaging and labeling activities within complex packaging operations
• Label Control:
  Works autonomously OR with limited supervision within established procedures
• Required to read, understand, follow, and review GMP documents
• Demonstrates mathematical skills, including the ability to perform addition, subtraction, multiplication, division, and conversions
• Collaborates and communicates with support teams
• Utilize the assigned logbook to document workstation line clearances
• Ensures batch readiness by gathering materials and documents required for such activities
• High attention to detail due to criticality of labeling process
• Verification and inspection of printed labels
• Gather and Issue pre-printed material component
• Perform reconciliation/destruction and return of printed materials

• High School Diploma/GED required
• Up to 2 years relevant experience
• GMP experience preferred
• Technical Requirements:
  Proficient with Microsoft Office programs, Email, Teams, etc.
• Ability to learn and use quality and…