Packaging Process Technician I – Accelerate Manufacturing

Novo Nordisk A/S

Clayton (NC)

On-site

USD 28,000 - 39,000

Full time

13 hours ago
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Benefits offered by this job

Health Insurance
Dental Insurance
Vision Insurance
8% 401K company match
14 holidays
Parental & family medical leave
Life & Disability Insurance
Employee product access

Job summary

Novo Nordisk A/S is seeking a Manufacturing Process Technician I (Packaging) for our Clayton, NC site. You will operate manufacturing equipment to support aseptic packaging and finish products, with supervision under the Shift Manager.

The role emphasizes safety, quality, and timely production delivery in a regulated environment. The ideal candidate has a high school diploma or equivalent and at least six months of manufacturing experience; experience in FDA-regulated settings is a plus.

Qualifications

  • High school diploma or equivalent required.
  • Six months minimum manufacturing experience required.
  • Experience in FDA-regulated environments preferred.
  • Production/manufacturing experience preferred.
  • Ability to read, write and understand product documentation and SOPs with attention to detail.

Responsibilities

  • Set up, operate, monitor & control equipment, systems & processes on production lines.
  • Execute production schedule to achieve goals.
  • Maintain production areas and perform cleaning.
  • Participate in event response and safety compliance.
  • Review and author SOPs and other documents as required.
  • Assist during equipment maintenance including predictive and preventative tasks.
  • Record/review production data in batch records and forms.
  • Follow all safety and environmental requirements.

Skills

Manufacturing experience
Attention to detail
Reading/writing SOPs

Education

High school diploma or equivalent

Job description

Novo Nordisk A/S is seeking a Manufacturing Process Technician I (Packaging) for our Clayton, NC site. You will operate manufacturing equipment to support aseptic packaging and finish products, with supervision under the Shift Manager.

The role emphasizes safety, quality, and timely production delivery in a regulated environment. The ideal candidate has a high school diploma or equivalent and at least six months of manufacturing experience; experience in FDA-regulated settings is a plus.

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