API Manufacturing Associate I - Pharma Production Impact

Novo Nordisk

Clayton (NC)

On-site

USD 52,000 - 70,000

Full time

35 hours ago
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Benefits offered by this job

Health Insurance
401K match
Paid time off
Tuition Assistance
Life & Disability Insurance
Parental leave
Product discounts

Job summary

Novo Nordisk is seeking a manufacturing operator for the API facility in Clayton, NC. The role focuses on operating automated equipment, adhering to GMP/cGMP standards, and supporting production goals within a clean room environment.

The position requires strong attention to detail, ability to read technical documentation, and teamwork in a fast-paced pharmaceutical setting. Training and safety programs are provided.

Qualifications

  • High school graduate or equivalent.
  • Associate's degree or higher in Tech, Science, or Engineering preferred.
  • BioWork or equivalent industrial training combined with experience preferred.
  • Minimum two years of manufacturing experience in FDA-regulated environment preferred.
  • Ability to read and understand complicated product documentation and SOPs with attention to detail.

Responsibilities

  • Operate API manufacturing equipment to meet production goals.
  • Follow GMP and cGMP standards and review SOPs and related documents.
  • Load and unload product from trucks, tanks, and ISO containers as required.
  • Review electronic batch records in real time for compliance with SOPs and GMP.
  • Maintain clean room areas and perform environmental monitoring as required.

Skills

Safety awareness
Reading SOPs
Problem solving
Teamwork

Education

Associate's Degree or higher in Tech, Science, or Engineering
BioWork or equivalent training

Tools

Microsoft Office
Computer-driven manufacturing equipment

Job description

Novo Nordisk is seeking a manufacturing operator for the API facility in Clayton, NC. The role focuses on operating automated equipment, adhering to GMP/cGMP standards, and supporting production goals within a clean room environment.

The position requires strong attention to detail, ability to read technical documentation, and teamwork in a fast-paced pharmaceutical setting. Training and safety programs are provided.

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