Job 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 www.agilent.com.

Will you join us in the fight against cancer?

We are seeking a temporary R&D Scientist to support our department with lifecycle management of our Pathology products. In this position, you will contribute to the product enhancement and lifecycle management of cutting-edge in vitro diagnostic devices that make a meaningful difference for patients around the world.

Your key responsibilities will include leading design control activities, driving product improvement initiatives, and maintaining our risk management documentation. All tasks will be carried out in compliance with applicable regulatory standards and guidelines.

Your tasks will include:

Planning, generation and update of Design Control documentation according to Agilent Quality Management System (QMS)Writing of study protocols and reports including data analysisDocument and specifications writingProduct care initiatives such as design changes to existing productsPost Market Surveillance activitiesComplaint handling when R&D support is needed for root cause investigationPlanning of R&D activities for projectsStakeholder management/communication (internal and external)Act as subject matter expert during internal audits and external inspections.Drive Continuous Improvement initiatives

You will be based at our Glostrup, Denmark office, working in a vibrant, dynamic, and diverse environment alongside approximately 26 colleagues. Our department is organized into two teams, and you will be joining one that includes 3 Design Responsibles, 8 R&D Scientists, and a Department Manager.

Qualifications

We are looking for a motivated individual with the following background:

Master’s/PhD in Biology, Biochemistry, Biotechnology or similar ¨Proven experience of at least 2 years within design control of Medical/Diagnostic devicesKnowledge of IHC (Immunohistochemistry), ISH (in situ hybridization) or special stains is a plusFull fluency in English. Note that Danish is not required

On a personal level, you are rigorous, driven and process oriented. You also have excellent interpersonal and communication skills to interact with many external and internal partners. You enjoy working both autonomously and as part of a team. Whilst being flexible and adaptable, you have also strong planning, organizational and time management skills.

What we offer:

Outstanding company cultureA position in an international and dynamic working place with exciting challenges and opportunitiesAn exciting and diverse work environment with many challenging tasksA chance to be part of the lifecycle support of state-of-the art IHC, ISH and primary stains products to the benefit of cancer patients, worldwideGreat colleagues and a strong team spiritMany opportunities for personal career and expertise developmentCompany pension scheme, individual bonus plan, private health care, medical & life insurance

We will make sure you get the training and development opportunities you need to become the best in your field.

Additional Details

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: No

Shift: Day

Duration: Over 12 Months

Job Function: R&D