Aseptic Process Engineer II – Growth & Innovation

Novo Nordisk

Clayton (NC)

On-site

USD 90,000 - 120,000

Full time

7 days ago
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Benefits offered by this job

Paid time off including holidays
Health Insurance
Dental Insurance
Vision Insurance
8% 401K contribution with companyMatch
Parental & family medical leave
Tuition Assistance
Life & Disability Insurance
Employee Referral Awards

Job summary

Novo Nordisk is seeking an experienced engineer to join FFEx in Clayton, NC, supporting development and installation of new equipment for aseptic and finished production to meet evolving business and regulatory requirements. The role emphasizes reliability, standardization, and cross-functional teamwork within a global setting.

The ideal candidate brings hands-on experience with autoclaves, CIP/SIP, and related cleaning/sterilization processes, plus a track record in pharmaceutical

Qualifications

  • Bachelor's degree in engineering or related field required.
  • Minimum 5 years of engineering experience in maintenance, design, or process improvement.
  • Knowledge of instrumentation, electrical, mechanical, and control systems.
  • Familiarity with RCA and RCM methodologies; Six Sigma Green Belt preferred.

Responsibilities

  • Develop new equipment and processes for aseptic and finished production.
  • Coach and mentor Engineering & Maintenance Technicians.
  • Support technical development and standards of the process.
  • Employ lean tools and problem-solving methods.
  • Work with global teams and vendors on equipment design.
  • Install and qualify new equipment and processes as part of the engineering team.
  • Maintain standards for procedures and maintenance plans.
  • Act as part of the DFP Technology Network team.

Skills

Autoclaves
CIP/SIP systems
Engineering experience

Education

Bachelor's Degree in engineering/related field

Job description

Novo Nordisk is seeking an experienced engineer to join FFEx in Clayton, NC, supporting development and installation of new equipment for aseptic and finished production to meet evolving business and regulatory requirements. The role emphasizes reliability, standardization, and cross-functional teamwork within a global setting.

The ideal candidate brings hands-on experience with autoclaves, CIP/SIP, and related cleaning/sterilization processes, plus a track record in pharmaceutical

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