Project Manager (36 month)

Description

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.

Will you join us in the fight against cancer?

Are you a project manager seeking new challenges? Perhaps you are an IVD or medical devices specialist looking to transition into project management.

We are seeking a Project Manager for a temporary period of 36 months to join the.

In Vitro Diagnostic Medical Devices (IVDR) Program Office, a newly created team within Agilent Pathology R&D, based in Glostrup, Denmark. The IVDR Program Office is responsible for driving the transition of Agilent’s existing IVD pathology portfolio to compliance with the European Regulation on (IVDR).

In this role, you will apply your project management skills and understanding of medical devices/IVDs to lead project teams to successfully transition Agilent Pathology products to IVDR.

Your Main Responsibilities will be:

Lead one or more projects to transition current cancer diagnostic IVDD products to IVDR. 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.

Communicate project status, progress, and challenges effectively.

Manage project risks including identification, mitigation, and contingency planning.

Manage relationships and inter-dependencies with other projects, and related activities.

Motivate and encourage your team

Act independently to identify and resolve challenges

Qualifications

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 ( Prince2, IPMA, PMP etc.) is a plus.

On a personal level, you are open minded, proactive, eager to learn and do not mind challenging the ‘norm’. You are curious and you enjoy solving problems. You also have great interpersonal skills to communicate internally and externally, working with a diverse group of stakeholders.At Agilent it’s where you embrace your curiosity and drive for innovation!

We offer:

The opportunity to be part of a new 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.

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

No

Schedule

Schedule:Full time

Shift

Day

Duration

Over 12 Months

Job Function

Administration