Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek -- so they can do what they do best: improve the world around us. Information about Agilent is available at www.agilent.com.
Join Agilent Denmark: Pioneering Cancer Diagnostics and Improving Lives
About Agilent Denmark
As a global leader in cancer diagnostics, Agilent Denmark is dedicated to maintaining the highest standards of quality and compliance, holding ISO 13485, IVD, IVDR, and MDSAP certifications. Our commitment to temperature-controlled storage and shipping ensures the safe delivery of our products to customers around the globe.
Your role: Logistics Admin & Support
We are looking for a passionate and skilled Logistics Admin to join our team consisting of 50 co-workers. In this role, you will support logistics processes, drive the Continuous Improvement (CI) program, drive projects, and ensure logistics compliance. Your work will directly impact patient diagnoses, making a real difference in people’s lives.
Key responsibilities:
CI lead: Lead the CI program to ensure improvements are successful.Project Management: Lead and manage logistics projects to enhance efficiency and effectiveness.Process Development: Innovate and improve logistics processes.Compliance Support: Ensure adherence to logistics compliance standards.Global Collaboration: Represent Agilent Denmark in global projects, working with colleagues worldwide.Additional Support: Driving or assisting with various administrative tasks.QualificationsA Bachelor’s in Logistics, Business Administration, or a related field.Proficiency in English (written and spoken); Danish is preferred.Very strong communication and presentation skills.Besides good MS Office working knowledge, experience with SharePoint is preferredAttention to detail.Experience with ERP systems, especially SAP, preferredWorking knowledge of Medical Device or other Regulated production (e.g., ISO 13485)1-5+ years of relevant experience.Special requirement:
Approval by PET to work as a Known Consignor.What we offer:
Independence and Collaboration: Enjoy an independent role within a supportive, growth-oriented team.Work/Life Balance: We are committed to helping you maintain a healthy work/life balance.Professional Growth: Opportunities to learn and advance in the field of Regulatory Affairs.Comprehensive Benefits: Including Agilent Result Bonus, Stock Purchase Plan, Life Insurance, Pension, Healthcare, Employee Assistance Program, generous holiday allowance, and engaging company activities.Join us at Agilent Denmark and be part of a team that is making a difference in the world of cancer diagnostics. Apply today and help us continue to improve lives through innovative solutions.
Additional Details
This job has a full time weekly schedule.Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locationsAgilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.Travel Required: OccasionalShift: DayDuration: No End DateJob Function: Manufacturing