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 hiring 2 R&D scientists for a temporary position (36 Months) to join us in the development and sustain of state-of-the art in vitro diagnostic devices to the benefit of patients throughout the world.

Your primary role will be to generate and update design control documentation for Pathology products. All work will be conducted in accordance with relevant regulatory guidelines and standards.

Your tasks will include:

Scientific contributorPlanning, generation and update of Design Control documentation according to Agilent Quality Management System (QMS)Sustain activities related to our Pathology Products such as design changes to existing products, or risk file maintenanceDrive Continuous Improvement initiativesStakeholder management/communication (internal and external)Planning of R&D activities for projects in close collaboration with project managersWork closely with cross-functional teams to engage in collaborative problem-solving, address challenges and ensure compliance through innovative and cooperative solutions.Serve as the key connector between R&D and other departments and facilitate effective communication and collaboration with various stakeholders to achieve common goals.

You will be based in our Glostrup, Denmark office, working in an exciting and dynamic diverse environment with around 24 colleagues. Our department is divided into two teams. The team you will join includes 3 Design Responsible, 9 R&D Scientists, and a Department Manager.

QualificationsMaster’s/PhD in Biology, Biochemistry, Biotechnology or similarKnowledge of IHC (Immunohistochemistry), ISH (in situ hybridization) or special stains is a plusExperience with Design Control, Risk Management, Design Changes or Manufacturing around Medical/Diagnostic devices is an advantageFull fluency in English. Note that fluency in 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