OBS! Ansökningsperioden för denna annonsen har
passerat.
Arbetsbeskrivning
Come join our dynamic team in a role where you will work with many different tasks and be able get insight in and learn more about quality and regulatory. We are a global company where you can really make a difference.
Don´t miss this opportunity!
Responsibilities:
coordination larger meetings within Quality/Regulatory Department
prepare agendas
note taking
distributions of meeting minutes
follow-up activities as needed
maintenance of Document Templates and Lists
general system/database administration
statistic collecting and reporting
supporting vigilance general monitoring
supporting external audits
supporting product registrations and tenders
Qualification / Background
Experience from similar tasks in a coordinator or administrative role
Well experienced in working with general Office package, specifically in One-Note, Sharepoint and Teams specifically
Comfortable in using English and Swedish language
Experience from work within Medical Devices company is desirable
In this role you will work with a lot of different tasks and contact settings. You will need to be service minded and flexible with a drive to take ownership and initiatives. We are looking for someone that is structured and well organized. It is also important that you are a team player.
We will evaluate candidates continuously so please send on your application as soon as possible or no later than June 24, 2021. Please send us your application in English.
We look forward hearing from you.