Software Design Control & Test Specialist

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

Want to go further in Research & Development for software products? Here's where you take the next step, working with the pioneering teams taking Agilent's world-leading products from the drawing board to the real world.
 
We are seeking a Software Design Control & Test Specialist for our software team in Glostrup, Denmark which is part of Pathology R&D in our Diagnostics and Genomics Group . We want to strengthen our software Lifecycle engineering activities to ensure efficient and successful progress in new or sustain software projects and maintenance of our high-quality portfolio of pathology staining instruments software for cancer diagnostics. As Software Design Control & Test Specialist , you will work with the team to accomplish activities and projects related to our software portfolio including software improvement projects/activities (such as feature enhancements and design optimizations based on customer feedback), software product care/sustaining activities as well as design control test & documentation.

Your key responsibilities will include:

• Execute software design control and test activities adhering to Agilent Quality Management System (QMS)
• Ensure Agilent’s pathology software products are in compliance with regulatory requirements
• Contribute to the product DHF and documentation according to internal and regulatory requirements
• Analyze and convert user needs to product requirements and user stories
• Act as Test responsible for design verification execution including establishment of an automated test suite.
• Collaborate with a broad range of stakeholders in the organization like Marketing, Procurement, Regulatory Affairs, Quality Assurance, Manufacturing, Developers and Global Service, Usability & Solution. 

This is a temporary contract of 2 years based in Glostrup (Copenhagen), where partial remote work would be an option (up to 2 days a week). 
 

Qualifications

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

• Ideally an engineering university degree in IT/Computer/Software , with a background in software product development 
• Experience within design control disciplines and/or Automated testing  
• Desire to work with documentation for requirements engineering, design verification, change control, risk management and defect management 
• Knowledge of regulated environments such as medical devices, pharma or similar would be a strong advantage
• Knowledge of medical standards IEC62304 is a plus
• Knowledge of / experience with Agile software development would be an asset
• Full proficiency in English . Proficiency in Danish would be a plus but is not a requirement

On a personal level, you can drive your activities while communicating and coordinating with various external and internal partners. You are dedicated and driven by results , which you reach by working closely with your colleagues within the team, as well as the rest of the organization. You are also well-structured and have a systematic way of working , seeking simple and effective solutions within the complexity that surrounds a medical device and the accompanying documentation package. You can work with day-to-day deadlines and changing priorities , as well as in projects with longer duration .

We offer:

• Outstanding company culture
• Career development opportunities
• Company pension scheme, individual bonus plan, private health care, medical & life insurance…
• A position within an international organisation, offering a dynamic working environment, with exciting challenges and opportunities

We will make sure you get all 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