Bemærk at denne jobannonce er udløbet!
Annoncen er udløbet, og stillingen kan ikke længere søges. Opslaget vises udelukkende som reference

QA IT Specialist

Job Description


We are looking for a QA IT Specialist to help us with the continuously improvement of Agilent's Computerized System Validation (CSV) process and Application Lifecycle Management.

You will be part of a great QA team and have direct responsibility for the QA oversight, supporting the implementation and improvement of our GxP IT applications, throughout the entire lifecycle.

Furthermore, you will be working closely with relevant process(es) stakeholders, ensuring an effective risk-based approach to CSV, in accordance with internal requirements and external regulatory requirements. KPIs and visual management is an important part of our workday, so efficiency and accountability are key skills in this role.

One of our missions at Agilent is to help our customers around the world fight cancer and other life-threatening diseases. By providing our customers with the best solutions to ensure accurate and early diagnosis, our aim is to improve patient treatment and enhance survival rates. This is your chance to contribute to this great mission.

In this role, you will be:

  • QA responsible in IT projects.
  • Supporting IT/CSV validation and change management activities.
  • Coordinating and participating in QA IT related projects.
  • Analyzing and evaluating systems and processes to improve work processes and service to internal customers.
  • Responsible for driving improvement projects in our team.
  • This is a great opportunity to also collaborate with a broad range of other departments including IT, RA, QA, Production, Marketing, etc.

    You will report into the Manager for the QA Process Department in Enterprise Quality Assurance & Regulatory Affairs.

    You will become a part of a company that live the values around innovation and contribution, uncompromising integrity, trust, respect and teamwork, speed, focus, and accountability.


    Qualifications


    Your profile:

  • Solid technical understanding gained through an engineering degree or other relevant, technical experience.
  • Min. 3 years of relevant experience with QA, preferably from the MDD/IVD industry.
  • Experienced within Computerized System Validation and GAMP 5.
  • Fluency in English, oral and written.
  • Danish language skills will be an advantage.
  • Familiar with ISO13485 and FDA regulations (21 CFR part 820, part 11).
  • Good planning, communication and stakeholder management skills.
  • Team player.
  • Result oriented and ambitious.
  • Adaptable and enjoy working in a high pace environment.
  • Questions:
    For further information about the position, please contact Hiring Manager Fouad Channir on +45 5162 8739 or Recruitment Partner Tinne Bigum on +45 8830 5115.


    Mere af samme slags?

    Modtag jobannoncer der minder om dette job i din indbakke.




    Når du tilmelder dig accepterer du samtidig vores privatlivspolitik. Du kan altid trække dit samtykke tilbage.

    Mere af samme slags?

    Modtag jobannoncer der minder om dette job i din indbakke.




    Når du tilmelder dig accepterer du samtidig vores privatlivspolitik. Du kan altid trække dit samtykke tilbage.