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Operator I, Inspection

2 years
Not Disclosed
10 Sept. 11, 2025
Job Description
Job Type: Full Time Education: B.Sc/ M.Sc/ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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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