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Location
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50% RA Medtech and 50% Pharma Administration

General
Youpal Group
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Sweden - Remote
March 4, 2025

Swedish, Compliance, Excel, Stockholm, Administrator, Pharma, Medtech

Deadline
2025-03-16
Work Level
Senior
Employee Type
Fulltime

Reply as soon as possible - we offer ongoing - attach CV in Word format, hourly price, accessibility, location and answer skills and should requirements.

Requirement profile
About the customer

Our customer has offices in central Stockholm and operates in Medtech and Pharma.


The assignment

50% of the assignment is about being coordinating about compliance with medtech products regarding MDR approval and other regulations in an international market.
50% is about registration of products in international system.Partly transfer from existing systems and new registrations.All according to new European legislation.


Requirement profile

You have a 3-5 year background in with tech in general and compliance in particular.You must have very good knowledge in European legislation on the tech area such as the EU MDR.You also have knowledge of other similar international legislation.
Experience from Pharma is also a merit.
You like to work with administrative tasks.
You are careful and good at managing large amounts of data.
You are communicative and master Swedish and English in both speech and writing.

You have good knowledge in Excel and a great interest in developing formulas and templates in Excel.

Other
The assignment is expected to start in mid -March and last until December.

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Job Description
I’m looking for a good designer as partner to work together on projects, that wants to expand his knowledge into the UX/UI and product area to collaborate on medium size projects. We will start with 20 hours per week and we might extend to full time after 2-3 months. First project is on financial instruments with blockchain as backend technology.
Requirements
On-site in United Arab Emirates
Have good communication skills and team working skill.
Know the principal of animation and you can create high quality prototypes.
Following design system guidelines
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