Senior Validation Engineer, Aseptic Manufacturing Leader

Biopharma Careers

Kongens Lyngby

On-site

DKK 651,000 - 957,000

Full time

13 days ago
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Job summary

Novo Nordisk in Lyngby is seeking a Sr. Validation Engineer to join the Manufacturing Technology team in Aseptic Manufacturing Technology Development & Innovation.

You will develop and implement validation strategies for our global aseptic production network, collaborating with process experts, QA and technical specialists to define requirements and risk assessments. The role offers exposure to cutting-edge technologies, engagement with external suppliers, and opportunities to contribute to

Qualifications

  • MSc or BSc in pharmacy, bioscience, chemical engineering, or a related field.
  • Experience working in a GMP-regulated environment.
  • Structured and detail-oriented approach to your work.
  • Strong communication skills and the ability to collaborate across disciplines.
  • Fluency in written and spoken English.
  • Advantage if you have experience with commissioning or validation of automated or computerised systems.

Responsibilities

  • Develop and execute global validation strategies, from planning through to verification
  • Facilitate workshops with process experts, QA and technical specialists to define requirements and risk assessments
  • Collaborate with automation and mechanical engineers to ensure strong documentation and test strategies
  • Support validation and implementation activities across global production sites.
  • Engage with external suppliers to ensure solutions meet Novo Nordisk standards

Skills

GMP experience
Fluent English
Cross-disciplinary collaboration
Structured & detail-oriented
Commissioning/validation of automated/

Education

MSc/BSc in pharmacy, bioscience, chemical engineering or related

Tools

Automation software

Job description

Novo Nordisk in Lyngby is seeking a Sr. Validation Engineer to join the Manufacturing Technology team in Aseptic Manufacturing Technology Development & Innovation.

You will develop and implement validation strategies for our global aseptic production network, collaborating with process experts, QA and technical specialists to define requirements and risk assessments. The role offers exposure to cutting-edge technologies, engagement with external suppliers, and opportunities to contribute to

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