Requistion ID: 78626
Wellspect Healthcare är en ledande global leverantör av innovativ medicinsk utrustning som hjälper människor med blås- eller tarmdysfunktion. Wellspect har fler än 1000 anställda runt om i världen som dagligen bidrar till att göra skillnad för alla de människor som behöver företagets produkter och tjänster.
Wellspect är en världsledande tillverkare av intermittenta urinkatetrar, där LoFric® är det mest kända varumärket. Företaget har också utvecklat Navina™, en lösning som hjälper mot kronisk eller allvarlig förstoppning och avföringsläckage. Navina™ är förmodligen marknadens mest avancerade irrigationssystem, en smart digital lösning som kombinerar hög användarvänlighet med klinisk effektivitet.
Wellspect strävar efter att bli klimatneutralt med minsta möjliga påverkan på miljön. Företaget har sitt huvudkontor i Mölndal, är verksamt i över 30 länder och är en del av Dentsply Sirona – världens största tillverkare av professionella dentala lösningar. Dentsply Sirona är listat på NASDAQ i USA under symbolen XRAY.
Besök www.wellspect.com eller www.dentsplysirona.com för mer information.
Process Engineer with Production Process Responsibilities
Join our Production Development team and continue shaping medical device production of tomorrow.
As our Process Engineer you will be responsible for one or more production lines and together with a cross-functional team secure that the processes consistently and efficiently are able to deliver high quality products. You and your cross-functional team will continuously improve the production process and eliminate root causes regarding e.g. technical failures and non-conforming products.
Responsibilities:
To be responsible for the change control within your area, including continuous process risk management and maintaining the validated state of the equipment. production process and eliminate root causes regarding e.g. technical failures and non-conforming products.
To be responsible for the change control within your area, including continuous process risk management and maintaining the validated state of the equipment. To be responsible for leading the daily nonconformity process regarding process and product. To lead a cross-functional coordination team from different departments. To support the Manufacturing organization in technical issues and identify areas where technical improvements are possible and/or necessary. To be involved when new or significantly changed products are affecting your process area, e.g. during the early stage of the project. We think you are a structured problem solver and efficient communicator. You also have an interest in bringing the best out of people and processes.
Background / Qualifications:
An academic background (M.Sc./B.Sc.) with experience from quality, manufacturing or production development within medical device or other business with high quality demands. Experience from automated manufacturing processes or chemical processes. Great analytical skills and that you are comfortable with driving changes and making decisions. Good documentation and communication skills, mainly in Swedish but also in English. Knowledge of Lean production concepts and experience from DMAIC and/or other Six Sigma methodologies.
Welcome with your application. Please note that we will review applications continuously, so be sure to send in your application as soon as possible.
We look forward hearing from you!