Job Title:
Manufacturing Associate – Inspection & Packaging
Location:
Bloomington, Indiana, United States
Job Category:
Manufacturing
About Novo Nordisk:
At Novo Nordisk, we’ve been leading diabetes care for over 100 years. Our Bloomington site is a state-of-the-art facility integrating process development, formulation, clinical and commercial biomanufacturing, drug product fill/finish, and packaging. Join a team where innovation meets impact, helping improve the quality of life for millions globally.
What We Offer:
Competitive pay with annual performance bonus
14 paid holidays and generous PTO
Health, dental, and vision insurance effective day one
8% guaranteed 401(k) contribution plus company match option
Family-focused benefits: 14 weeks paid parental leave, 6 weeks family medical leave
Free access to Novo Nordisk-marketed pharmaceutical products
Tuition assistance, life & disability insurance, and employee referral awards
Mentorship, resources, and career growth opportunities
Position Summary:
Operate and maintain manual and semi-automated visual inspection and packaging processes to achieve production goals.
Shift:
3rd Shift – Sunday to Thursday, 11:00 PM to 7:30 AM
(Shift may change based on business needs; candidates must be flexible.)
Reports To:
Manufacturing Supervisor
Key Responsibilities:
Inspection & Packaging:
Entry-level role with training; tasks are supervised and clearly defined
Safely operate basic equipment and support cleaning/organization of work area
Follow GMP documents and participate in continuous improvement initiatives
Report safety and quality concerns, recommending improvements
Inspection Duties:
Manual visual inspection of product families
Operate Semi-Automated Syringe and Vial Inspection systems
Work within fully automated inspection processes
Perform inspection while sitting in a lighted booth for 12-hour shifts
Packaging Duties:
Construct secondary and tertiary packaging for finished products
Perform manual packaging, labeling, and palletization per specifications
Stand for 12-hour shifts and support complex packaging operations
Label Control Duties:
Verify, inspect, and reconcile printed labels
Document workstation line clearances using assigned logbooks
Gather and issue pre-printed material components
Ensure batch readiness and high attention to detail
Qualifications:
Education & Experience:
High School Diploma/GED required
Up to 2 years relevant experience; GMP experience preferred
Technical Skills:
Proficient in Microsoft Office, email, Teams
Ability to learn quality and operations software (ERP: J.D. Edwards®, ComplianceWire®)
Basic understanding of production operations and cGMP/GDP compliance
Strong mathematical skills (addition, subtraction, multiplication, division, conversions)
Behavioral Skills:
Effective communication in English (verbal and written)
Detail-oriented, organized, and able to manage time under high-pressure situations
Ability to work independently or in a team environment
Lead by example and uphold company values and culture
Leadership (if applicable):
Build relationships and trust with peers and departments
Take initiative for personal/professional growth and problem-solving
Physical Requirements:
Frequent sitting (up to 12 hours), standing, walking, reaching, talking, writing, and use of computers
Occasional stooping, kneeling, crouching, bending, lifting up to 35 lbs
Work in a cleanroom environment and comply with EHS responsibilities
Vision requirements must be met
Diversity & Inclusion:
Novo Nordisk is committed to an inclusive recruitment process and equal opportunity employment. We value diversity in perspectives, backgrounds, and cultures. All qualified applicants will receive consideration without regard to race, ethnicity, color, religion, gender, sexual orientation, disability, veteran status, or other legally protected characteristics.
Accommodation Requests:
If you require assistance applying, call 1-855-411-5290. (This number is for accommodation requests only.)
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