Novo Nordisk

Product Development Engineer

Novo Nordisk

full-time

Posted on:

Location Type: Office

Location: HillerødDenmark

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About the role

  • Lead the development of life-saving packaging systems where technical expertise meets project leadership—and your work protects both product quality and patient safety.
  • Take on a unique hybrid role that combines hands-on technical development of primary packaging with coordination and project leadership responsibilities.
  • Develop robust, compliant packaging systems for parenteral administration while driving cross-functional projects from concept through to delivery.
  • Develop primary packaging systems and components (e.g., vials) including specifications, drawings and test documentation that meet regulatory and industry requirements.
  • Take ownership for planning and coordinating project execution: setting clear goals, managing timelines, resources and budgets, and monitoring progress to meet scope, quality, schedule and cost targets.
  • Lead and engage cross-functional project teams, fostering a committed project culture and ensuring effective governance is in place.
  • Contribute to safety risk management, requirement engineering and medical device development activities.
  • Coordinate and collaborate with external suppliers and manufacturers throughout development and transfer activities.
  • Drive change requests, troubleshoot technical issues and participate in systematic problem-solving across development activities.
  • Report project performance to stakeholders and perform integrated change control while ensuring compliance with Novo Nordisk Quality Management System.

Requirements

  • M.Sc. or B.Sc. in Engineering, Pharmacy, or related field with at least 3 years' relevant experience (M.Sc. with 3+ years or B.Sc. with commensurate experience is considered advantageous)
  • Practical experience with regulatory requirements and standards for primary packaging and understanding of GMP environments
  • Experience in requirement engineering, safety risk assessment, and Parenteral or medical device development
  • Demonstrated ability to coordinate cross-functional projects, manage stakeholders and deliver on milestones
  • Fluent in both written and spoken English
  • Strong analytical, systematic approach and a quality mindset, with excellent communication skills and the ability to manage multiple tasks in parallel
  • 4+ years' project management experience or formal project management certification (nice to have)
  • Experience in leachables/extractables, GMP material documentation, and system engineering (nice to have)
  • Training in Lean methodologies and experience mapping or improving working processes (nice to have)
Benefits
  • A unique opportunity to work in an internationally diverse and highly skilled team at Novo Nordisk with state-of-the-art R&D facilities.
  • You'll benefit from professional development opportunities and broad exposure across technical development and project execution.
  • We are committed to being inclusive and diverse and support career growth across our organization—all within a culture that values curiosity, collaboration, and a focus on patient outcomes.
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
packaging systems developmentprimary packagingspecificationsdrawingstest documentationrequirement engineeringsafety risk assessmentproject managementGMP documentationsystem engineering
Soft Skills
project leadershipstakeholder managementanalytical skillscommunication skillsorganizational skillsproblem-solvingcross-functional collaborationquality mindsetability to manage multiple taskscommitment to project culture
Certifications
project management certification