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Responsible Engineer for Expansion Projects, Process Engineering

FUJIFILM Diosynth Biotechnologies (FDB) in Hillerød, Denmark continues to expand. We are now starting the new Large Scale Manufacturing Facility Expansion Project and Process Engineering is looking for Responsible Engineers/Package Owners for the new expansion project. We support equipment from solution preparations, through cell culture and harvest to downstream purification operations.

Our Process Engineering department supports process equipment through all phases of the equipment lifecycle – from design, through commissioning and validation activities, in daily operations and changes required to support new process introductions and optimizations. Responsible Engineers are required to make independent decisions based on risk assessment for the design and testing of equipment. We value safety first and have high quality standards.

You will be equipment engineer in the major facility expansion project, where your technical expertise will be needed for ensuring equipment is designed, manufactured, and tested according to specifications. Travel activities are required as part of the project for vendor and factory visits and test activities. In later stages of the project, you will be part of troubleshooting in relation to commissioning and validation.

The role is part of the process engineering group, which is split into two different teams  upstream and downstream. Each team  consists of 12-15 people, who all support each other regardless of individual responsibility. We strongly value collaboration and knowledge sharing. We offer a culture with happiness at work – where we support each other and celebrate our successes.

Responsibilities 

  • Process Engineer in large scale CAPEX projects
  • Creating, reviewing, and ensuring compliance towards equipment specifications
  • Perform equipment walkdowns, supervise coverage testing during factory acceptance testing
  • Review of 3D design models
  • Provide functional specifications/descriptions of unit operations as required
  • Review validation protocols and support commissioning and validation testing
  • Troubleshoot during testing, validation, and commercial manufacturing activities

Requirements

  • Minimum a Bachelor’s Degree within engineering or similar discipline
  • 5+ years of experience in the areas of GMP manufacturing, engineering, or facilities in a pharmaceutical environment
  • Enjoy working as part of a team and also being comfortable working independently
  • Great stakeholder management skills
  • Results-oriented
  • Self-driven
  • Fluent in English both verbal and written  

Has this sparked your interest? Then we urge you to apply as soon as possible. We will continuously invite relevant candidates for job interviews and will close the position as soon as we have found the right candidate. Due to summer vacation, delayed response can be expected.

Degrees of interest: Bachelor’s Degree within engineering

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