Project Manager/Senior Project (12-month parental leave cover)
Job Description
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Background
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 us in the fight against cancer
Are you a project manager passionate about playing a key role in advancing cancer diagnostics? Or do you bring expertise in IVD or medical devices and want to step into project leadership?
We are looking for a Project Manager / Senior Project Manager to join our In Vitro Diagnostic Regulation (IVDR) Program Office in Glostrup, Denmark, where you will play a key role in transitioning Agilent’s pathology portfolio to compliance with the European Regulation on in vitro diagnostics.
This is a unique opportunity to contribute directly to the availability of high\-quality cancer diagnostics for patients worldwide.
Your Main Responsibilities will be:
- Lead one or more IVDR transition projects for cancer diagnostic products. This may include delivery of technical file documentation, submission to a notified body, and ensuring manufacturing readiness.
- Develop project plans, budgets, and resource plans in collaboration with stakeholders.
- Lead geographically diverse, cross\-functional project teams, including, but not limited to, Marketing, Research and Development, Regulatory, Quality Assurance, and Manufacturing.
- Monitor project progress and communicate status, risks, and mitigation plans to stakeholders
- Manage risks, dependencies, and cross\-project interfaces
- Proactively resolve challenges and drive decision\-making
- Foster alignment, accountability, and engagement within project teams
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We are looking for a motivated individual with the following background:
- A relevant Master’s background related to Life Science or Engineering.
- Experience with coordination of project teams and proven success in delivering results in a highly regulated industry.
- Solid understanding of working with design control documentation for *in vitro* diagnostic or medical devices.
- Strong collaboration, stakeholder management and communication skills to align and set direction for project teams
- Excellent English verbal/written communications skills.
- Problem solving, planning and analytical skills.
- Ability and flexibility to manage uncertainty, ambiguity, and changes in direction in a fast\-paced work environment.
- Knowledge of IVDR is a plus.
- Certification in Project Management (e.g. Prince2, IPMA, PMP etc.) is a plus.
We offer:
- The opportunity to be part of a dynamic team
- A role among passionate colleagues, in a growth orientated and inclusive environment. You will become part of a caring and fast paced environment, built on integrity, sharing and trust.
- A chance to be part of the lifecycle management of state\-of\-the\-art diagnostic assays, benefiting cancer patients worldwide
- An international work environment
- A commitment to work/life balance.
- Career development opportunities in an international company.
- Competitive compensation and benefits package.
This job has a full time weekly schedule.
Agilent 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:
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DayDuration:
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0\-3 MonthsJob Function:
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R\&D
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