The ideal candidate will have:
· 1 to 3 years of experience in document control, quality assurance, or regulated environments
· Intermediate to advanced skills in Microsoft Word and Excel
· Highschool diploma or GED
· Strong attention to detail and organizational skills
· Strong communication skills, with the ability to coordinate effectively across multiple functions and in a cross-cultural environment
· A reliable, structured, and adaptable work approach, with a consistent ability to meet deadlines
· Experience with Agile or product lifecycle/document management systems (preferred)
· Coordinate implementation activities related to label and IFU updates in close collaboration with teams in Carpinteria and Glostrup, Denmark
· Act as a key point of contact across multiple functions, including project managers, Label Subject Matter Experts, production, procurement, and external partners
· Manage contact with external suppliers, such as translation vendors and IFU print providers
· Update Raw Material Specifications (RMSs) related to IFUs
· Ensure that project deliverables are completed in alignment with agreed project plans and timelines
· Register work time for cross-charging in Agilent’s time-keeping system
In this role, you will support and drive the implementation of label and (IFU) updates for In Vitro Diagnostic (IVD) products, ensuring timely and compliant execution of all activities. This will be done in close collaboration with cross-functional teams based in both the US and Denmark.
You will be organizationally part of the Labeling & Packaging Material team, which currently consists of 10 employees in Denmark (including the hiring manager) and 1 employee in the US.