Job Information
Dentsply Sirona Process Manager - Mölndal, Sweden in Molndal, Sweden
Requistion ID : 75652
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 Manager
Join our Production Development team and continue shaping medical device production of tomorrow.
As a Process Manager 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.
Wellspect is proud to have an in-house, highly automated medical device production. We have strict requirements on traceability and in-line quality control. Data collection and the ongoing initiatives to further facilitate analysis and visualization of the data give the Process Manager and the rest of the team great possibilities to analyze data and suggest and perform improvements.
Responsibilities :
To be responsible for the change control within your area, including continuous process risk management and maintaining the validated state of the equipment.
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 when the requirements are set and during planning and completion of the final stages with validation, launch and ramp-up.
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.
Qualifications / Background:
proven leaderships skills in leading teams and experience in driving changes.
an academic background, preferably in automation/electrical/mechanical engineering or equivalent with experience from production or process engineering.
knowledge of automated manufacturing processes.
knowledge of Lean production concepts and experience from DMAIC and/or other Six Sigma methodologies.
experience from working with technical specifications and change control.
some experience from testing/validation, preferably within life science or other regulated industry.
documentation and communication skills in Swedish and English.
it is also an advantage if you have experience in Power BI and data visualization.
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!