Project Support Engineer

at  Novo Nordisk

Project Support Engineer
Category: Manufacturing
Location:Køge, Region Zealand, DK
Do you dream about working daily to ensure and live up to good engineering and manufacturing practice in exciting projects? Is ‘validation’ your middle name? Are you ready to bring your expertise and knowledge to a higher level while working with highly skilled colleagues?
Then you might be the Project Support Engineer we are looking for! Read on and apply today!

QUALIFICATIONS

To succeed in this role, you have:

• A min. bachelor’s degree in pharmaceutical engineering, chemical engineering, mechanical engineering, automation engineering or similar technical and/or life sciences background.
• Experience with Good Manufacturing Practice (GMP) from production environment, within production equipment, utilities, automatization, process validation, operational process, design of equipment and installations, validation and/or qualification.
• Ability to make concrete requirements to production equipment and some knowledge within automation, regulation, and measurement techniques.
• A flair for IT and automation.
• Full professional proficiency in English and Danish.

As a person, you are a dedicated team player, who enjoys witnessing the team’s success and taking pride in everyone’s contributions brings great energy. Thriving in this role requires the ability to find solutions to problems and maintain a positive and constructive mindset in the face of adversity.
We will welcome a colleague who finds working with IT systems easy and is curious about new technology within data collection and improvements.

The main tasks will be to:

• Make suggestions for design, equipment, components, and physical construction.
• Contribute to the implementation of engineering standards, which ensures that all technical, quality- and safety inputs are adjusted and implemented.
• Participate in end-to-end processes (determining business needs, creating user requirements specifications, designing solutions, and writing documentation such as procedures and change requests).
• Implement operational standards and ensure that all quality and safety input are adjusted and implemented.
• Approve Acceptance Criteria for URS requirements - Acceptance Criteria for PQ, PV, System Acceptance and Release (SAR) and Decommissioning Plan and report

To succeed in this role, you have:

• A min. bachelor’s degree in pharmaceutical engineering, chemical engineering, mechanical engineering, automation engineering or similar technical and/or life sciences background.
• Experience with Good Manufacturing Practice (GMP) from production environment, within production equipment, utilities, automatization, process validation, operational process, design of equipment and installations, validation and/or qualification.
• Ability to make concrete requirements to production equipment and some knowledge within automation, regulation, and measurement techniques.
• A flair for IT and automation.
• Full professional proficiency in English and Danish