Agilent

Supplier Quality Specialist (BB-7ACFF)

Found in: Neuvoo DK

Description:

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 enhancing their chances of treatment and ultimately their chances of survival. This is what we since 1967 (and originally name of Dako) and to this date what 700+ employees in Glostrup have had as their function, either through the research & development, production and sales of diagnostic reagents, or via our automation of processes and diagnostic product portfolio.

Are you our new QA Specialist for our Supplier Quality Assurance team? Are you passionate about working with suppliers? Then we have an interesting opportunity for you. You will work with a team of highly enthusiastic and dedicated team of Supplier QA specialists.

To perform this job successfully, the employee will possess the skills, aptitudes, and abilities to perform the essential duties proficiently.

  • Work with Procurement department to ensure supplier performance is regularly reported and that appropriate and timely corrective actions are implemented
  • Supplier approval process
  • 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
  • Support Quality agreements with critical supplier
  • Secure good collaboration between relevant stakeholders across the organization and business units.
  • Secure good collaboration between different stakeholders

  • Qualifications


  • Solid experience of QA/RA related work, preferable within Supplier handling
  • Furthermore, a Bachelor or Master degree in Engineering, Biochemistry or related field of study experience, combined with experience from IVD, Medical Device or Pharma industry.
  • Furthermore, you have strong skills in more of the areas listed below:

  • Knowledge of global complaint handling requirements within medical devices/IVDs
  • Understanding of Quality System Regulations 21 CFR part 820 and ISO-13485.
  • High degree of personal drive, proactiveness and responsibility.
  • Effective communication at all levels, internally and externally, including sound stakeholder management experience
  • Solid understanding and application of business concepts and practices, including a desire to work in a fast-paced and dynamic environment.
  • Questions
    If you have questions about this position or our application system please contact the recruiter, Cecilia Bengtsson on cecilia.bengtsson@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.


    calendar_today4 days ago

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