Quality Technician

at  PhillipsMedisize

7600 Struer, Region Midtjylland, Denmark -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate20 Oct, 2024Not Specified21 Jul, 2024N/ACollaboration,English,Kaizen,Sap,Instructions,Documentation,Medical DevicesNoNo
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Description:

Your Job
We are looking for a committed and independent employee for our quality control department, which is a key player in ensuring that our customers always receive the expected quality.

WHO YOU ARE (BASIC QUALIFICATIONS)

  • Have a background as a quality or production employee
  • Possess experience operating measuring tools and assessing surfaces
  • Have a willingness and desire to perform responsibly and well in collaboration with your colleagues in the team
  • Possess good IT skills, preferably experience with SAP and the Office suite
  • Work in a structured and systematic way
  • Are good at prioritizing your time
  • Have good collaboration skills regardless of professional group
  • Have a desire to learn new skills.
  • Can speak and understand English at an intermediate level or higher

WHO WE ARE

As a Molex company, Phillips-Medisize mobilizes and deploys specialized capabilities and services across highly regulated industries, including health care, regulated consumer, automotive and defence. We design, develop and create innovative and lifechanging medical technologies for millions of people around the globe.
At Koch, employees are empowered to do what they do best to make life better. Learn how our business philosophy helps employees unleash their potential while creating value for themselves and the company.
Additionally, everyone has individual work and personal needs. We seek to enable the best work environment that helps you and the business work together to produce superior results.

LI-JO

Responsibilities:

You will be part of the QC team, which is responsible for planning, executing and documenting your own work tasks. The team have a wide range of cross functional interactions in the company - from goods receipt to development engineers. We sometimes have a busy workday, but we are good at listening and helping each other.

As a developer and manufacturer of medical devices, there are high quality and documentation requirements for our work. The tasks in the team are diverse, where your primary tasks will be:

  • Incoming and outgoing inspection of items according to instructions
  • Documentation of performed checks on PC
  • Line clearance in production and documentation thereof
  • Control of equipment that needs to be calibrated
  • Be part of continuous improvement activities like 5S, Kaizen, etc.


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Other Industry

Pharma / Biotech / Healthcare / Medical / R&D

Other

Graduate

Proficient

1

7600 Struer, Denmark