MedTech Quality Assurance / Regulatory Affairs (QA/RA) specilist

Brainlink AB / Administratörsjobb / Göteborg
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Brainlink is looking for a Quality Assurance / Regulatory Affairs (QA/RA) specialist

About Brainlink
Brainlink AB is a Swedish medical technology startup sprung from the inside perspective of neurosurgery. Our core focus is to integrate today's technology into existing treatments that globally affect more than a miilion patients yearly. We aim to create breakthrough medical devices for more effective diagnostics and treatment of neurological conditions, while saving resources for hospitals and healthcare staff worldwide.
Who are we looking for
We are looking for a Quality Assurance / Regulatory Affairs (QA/RA) specialist with a passion to transform healthcare through assisting in solving complex design problems. In this role you will work together with our team of engineers and management, taking on activities related to all areas of the product development cycle. You have excellent organizational and project management skills.
Background
As QA/RA specialist, you will participate in key cross functional activities in support of medical device development. In this role you are expected to be readily available and flexible to support a broad range of technical needs of the company.

In this role, your responsibilities will include:
Developing and sustaining Brainlink's Quality Management System for Regulatory Compliance.
Participate in activities related to ideation, valuation, testing and verification of product development.
Work collaboratively with the engineering and management team.
Communicate effectively within the team as well as with external touchpoints.
Support in keeping the timeline of delegated internal and external tasks, report progress and status through weekly updates.
Application of standards and standard operating procedures for the product development.

Required qualifications
University degree (MSc or equivalent) in engineering or biomedicine.
Minimum 2 years experience in QA / RA in medtech product development.
Experience in medtech product development.

Recommended qualifications
Experience in regulatory assurance for medical implants.
Experience in medical technology development.
Experience working with sensor systems and/or wireless signaling in a medical environment.

Brainlink offers you
Use your experience to improve healthcare outcomes and make a real difference to patients around the world.
Participate in creating a new paradigm within MedTech.
The opportunity to work at arm's length from clinical medicine.
A work experience that is challenging and rewarding, with space for independent thinking, innovation, and growth.

Salary: To be discussed
Employment conditions: Full- or part time (minimum 50%)
Location: On site: Gothenburg, Sweden. Candidates preferably currently based in Gothenburg, but we do welcome applications from citizens located outside Sweden.
EU Visa is mandatory.
Öppen för alla
Vi fokuserar på din kompetens, inte dina övriga förutsättningar. Vi är öppna för att anpassa rollen eller arbetsplatsen efter dina behov.

Så ansöker du
Sista dag att ansöka är 2024-08-18
E-post: brainlinkab@gmail.com

Arbetsgivarens referens
Arbetsgivarens referens för detta jobb är "MedTech QA/RA specialist".

Omfattning
Detta är ett heltidsjobb.

Arbetsgivare
Brainlink AB (org.nr 559370-7259)
Medicinaregatan 8 A (visa karta)
413 90  GÖTEBORG

Jobbnummer
8791613

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