Internship at QAdvis

We are happy to welcome Sneha Bangalore to QAdvis. Sneha has been hired via Jobbsprånget as an intern and will be a part of our teams in both Stockholm and Lund. She has recently finished her master’s degree in applied biotechnology from Uppsala University. During her master she has among other things studied molecular biotechnology, immunotechnology, nanobiotechnology, biosensors and microfluids. Sneha will support us in various projects. She has experience in testing and analysing,for example in microbiology and molecular biotechnology laboratory techniques including bioassays ELISA, SDS-PAGE, DNA studies and biosensor projects.

Sneha Bangalore:
“I am really happy about this internship and I look forward to get an introduction to Quality and Regulatory consulting within medical and in-vitro diagnostic medical devices. This opportunity will broaden my understanding in quality management systems and give insights into Swedish work culture. I am grateful for the amazing mentors and very understanding work environment at QAdvis”

 

Career at QAdvis

To our offices in Lund and Stockholm we are now looking for new colleges that will work together with us and our clients as Quality & Regulatory consultant within the Medical Device and In Vitro Diagnostic medical device industry.

Read more here

Welcome Noomi

We are very pleased to announce the joining of our new colleague Noomi Altgärde and extend a warm welcome to the QA&RA consultant team at QAdvis!

Noomi has a PhD in Bioscience and a long background from working with medical devices in the development phase, with a focus on quality assurance and regulatory affairs. Her curiosity and broad background within both research and product development gives an excellent platform to understanding the complexities medical device manufacturers will face, simplifying regulatory requirements and finding hands-on solutions for both manufacturers and other stakeholders.

Read about technical documentation here.

 

2-day course EN ISO 13485:2016

The harmonised EN ISO 13485:2016 standard can be used to show compliance with the regulations and constitutional requirements needed for companies supplying medical devices and associated services in the EU