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Supplier Quality Specialist

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. .

Our mission at Agilent is to help our global customers in fighting cancer and other life threatening illnesses. Our contribution is in providing the best possible tools for precise and fast diagnosis of patients, thereby improving treatments and ultimately their chances of survival. This is what we have been doing since 1967 (and originally name of Dako) to this date. A company of 700+ employees in Glostrup with the same goal either through research & development, production and sales of diagnostic reagents, or via our automation of processes and diagnostic product portfolio.

We are looking for our new QA Specialist to join our highly enthusiastic and dedicated Supplier Quality Assurance team. If you are passionate about working with suppliers then we have an exciting opportunity for you.

To achieve success in this role the ideal candidate will possess the skills and aptitude to perform the crucial duties proficiently. The ability to apply a quality mind-set and knowledge of current regulations to deliver change.

  • Work with Procurement department to ensure supplier performance is regularly reported and that appropriate and timely corrective actions are implemented.
  • Supplier management from approval and quality agreement.
  • Manage critical supplier audit system and schedule
  • Review supplier manufacturing processes, collaborate with suppliers on process improvement and value enhancement opportunities
  • Establish specific short / long term supplier quality goals-KPIs
  • Support the SCAR process
  • Secure good collaboration between relevant partners across the organization and business units.

  • Qualifications


  • Demonstrated experience of QA/RA related work in IVD, Medical Device or Pharma industry, preferably within Supplier handling
  • Understanding of Quality System Regulations 21 CFR part 820 and ISO-13485, Medical Device Singe Audit Program
  • High degree of personal drive, pro-activeness and responsibility.
  • Effective communication at all levels, internally and externally, including partner management experience
  • We offer:

  • Training and development opportunities.
  • A commitment to work/life balance.
  • An independent job among good colleagues, in a growth orientated conglomerate. You will become part of a caring and fast paced environment, built on integrity, information and trust.
  • In addition, you will have the opportunity of becoming part of a company which has the following values: We develop cancer diagnostics, taking it a step further, ensuring the best possible precise and fast diagnosis.We have a deep interest in the needs of our customers and cancer patients, doing our best to people being treated with respect and decency.We value quality in the solutions we deliver to our customers, with our employees and in relation to the processes we work with.
  • Questions

    If you have questions about this position or our application system please contact the recruiter, Sandra Anyanwu on sandra.anyanwu@non.agilent.com.

    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.



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