Oferta: Technical Documentation Coordinator

Technical Documentation Coordinator
Miejsce pracy: Szczecin

3Shape is the “Google” of the dental industry, the leader of the dental CAD/CAM market. We are specialists in the production of 3D scanners, present in Poland for over 10 years.

 

To support further growth, we are looking for Technical Documentation Coordinator for our Product Lifecycle team of around 15 mechanical, electronics and software engineers. The team works on improving the quality of products in the field and efficiency in production by conducting production near RD in close collaboration with Global Quality, Production, Procurement and Support as well R&D colleges from Denmark and Ukraine.

 

The position is based in the R&D department at our Production facility in Szczecin (Poland).

Our offer:
  • Competitive employment terms and benefits
  • Stable employment conditions (contract of employment)
  • Personal growth and development through continuous learning
  • The chance to influence the future of a rapidly expanding company
  • Informal atmosphere, among best-in-class colleagues with a strong emphasis on supporting creativity and fostering well-being of the employees An attractive work environment in a brand-new production facility with canteen and observation deck.
  • No worries about lunch - you can buy it in our canteen for only 2 PLN
  • Company events
Job Description


We are looking for a systematic and structured engineer to conduct and document product changes to improve quality, production efficiency and drive down cost.

 

To thrive and succeed in the position you should be good at following set processes and procedures and finishing tasks. We imagine that you are good at making and following checklists, can review technical documentation to see if it is compliant and can suggest improvement to make our processes can be improved to become more efficient.

 

You will both work on your own changes and support the team of R&D engineers in everyday activities by coordinating the administrative work around product and tooling design changes, as well as corrective and preventive actions (CAPAs).

 

The work will be carried out in close collaboration with both local Engineers in Poland and R&D engineers from Poland and Denmark.

 

Your role:


In your new job you will:

  • Support R&D engineers in processing and filing highly technical and specific information
  • Perform systematic review of changes implementation status and documentary finalization of completed changes
  • Follow up on actions required by product change procedures
  • Have a continuous dialog with the stakeholders (QA, R&D, Production)
  • Maintaining lists of ongoing product changes and activities around them (e.g., corrective actions, sourcing issues)
  • Communicate the Product Changes overview on regular basis
  • Prioritizing the tasks within Product Changes
  • Creating, updating and approving quality and production documentation according to company needs
Candidate profile


The ideal candidate is hands-on, implementer with some years of experience within development or production of technical products and has:

  • B.Sc., M.Sc in Quality Engineering, Quality Management or related
  • Experience with quality and validation processes
  • Experience in production of medical devices is a big advantage
  • Experience in performing root cause analysis of failures
  • Strong technical skills and fundamental understanding
  • Fluent English
  • Knowledge of: Microsoft Office and SolidWorks
  • High communication skills
  • Comfortable in interdisciplinary and international environment
Job Description


We are looking for a systematic and structured engineer to conduct and document product changes to improve quality, production efficiency and drive down cost.

 

To thrive and succeed in the position you should be good at following set processes and procedures and finishing tasks. We imagine that you are good at making and following checklists, can review technical documentation to see if it is compliant and can suggest improvement to make our processes can be improved to become more efficient.

 

You will both work on your own changes and support the team of R&D engineers in everyday activities by coordinating the administrative work around product and tooling design changes, as well as corrective and preventive actions (CAPAs).

 

The work will be carried out in close collaboration with both local Engineers in Poland and R&D engineers from Poland and Denmark.

 

Your role:


In your new job you will:

  • Support R&D engineers in processing and filing highly technical and specific information
  • Perform systematic review of changes implementation status and documentary finalization of completed changes
  • Follow up on actions required by product change procedures
  • Have a continuous dialog with the stakeholders (QA, R&D, Production)
  • Maintaining lists of ongoing product changes and activities around them (e.g., corrective actions, sourcing issues)
  • Communicate the Product Changes overview on regular basis
  • Prioritizing the tasks within Product Changes
  • Creating, updating and approving quality and production documentation according to company needs
Candidate profile


The ideal candidate is hands-on, implementer with some years of experience within development or production of technical products and has:

  • B.Sc., M.Sc in Quality Engineering, Quality Management or related
  • Experience with quality and validation processes
  • Experience in production of medical devices is a big advantage
  • Experience in performing root cause analysis of failures
  • Strong technical skills and fundamental understanding
  • Fluent English
  • Knowledge of: Microsoft Office and SolidWorks
  • High communication skills
  • Comfortable in interdisciplinary and international environment
Please add consent for processing personal data included: In accordance with the Law of Personal Data Protection of 29.08.1997 (Journal of Laws No. 133, item 883) I give my consent to processing of my personal data contained in my application for the purpose of current and future recruitment process within 3Shape Group.In accordance with art. 24 sec. 1 of the Act of 29 August 1997 on the Protection of Personal Data (Journal of Laws of 2002, No. 101, item 926, as amended), we inform you that the administrator of personal data provided by you voluntarily to conduct current and future recruitment is 3Shape Poland Sp. z o. o. with headquarters in Szczecin 71-001, at Południowa 27C. You have the right to access, correct and delete your personal data. Please be advised that, apart from the entities authorized under the law, the collected personal data will not be made available. Your personal data will be kept for a period of 12 months.Please be informed that the 3Shape Poland Sp. z o. o.  uses closed circuit television (CCTV) images to provide a safe and secure environment for employees and for visitors to the 3Shape Poland Sp. z o. o. business premises as well as to protect the 3Shape Poland Sp. z o. o. property and assets. The CCTV system may be used to investigate security incidents in order to secure evidence, should such incidents occur. All footage gathered is stored no longer than 30 days. The images that are filmed are recorded centrally and held in a secure location.
APLIKUJ TERAZ

Szczegóły oferty

Stanowisko: Technical Documentation Coordinator
Firma: 3SHAPE POLAND SP. Z O.O.
Miejsce pracy: Szczecin
Opublikowano: 2022-01-13