You are a driven and brilliant QA/RA specialist with a passion for innovation in medical software! You want to be part of a knowledge-driven and inspiring team aiming Beyond Tomorrow. You will have the opportunity to work on exciting and challenging projects that secure the future of health. You have a sharp mind that loves to develop smart solutions and contribute to extraordinary results. Are you ready to join us and make a real difference?
This will be your role
As a Medical Software QA/RA Specialist with us, you will lead the quality efforts for our cutting-edge medical devices. You will have the opportunity to work both independently and in close collaboration with our dedicated and caring colleagues, where we jointly strive to reach new heights and exceed customer expectations.
Your extensive experience in medical device software development and your deep understanding of regulatory requirements and quality standards are essential to ensure that our products meet the highest standards. You will play a key role in understanding and implementing these requirements in our customers' development processes.
You will have the opportunity to:
- Develop, optimize and digitalize quality and regulatory work around software development of medical devices together with our customers.
- Influence your own development by taking an obvious Location in our knowledge-sharing forums and by driving and developing our offer.
- Build good long-term relationships with our customers to understand and meet their specific needs.
Here's how you'll shine
We're looking for someone who takes initiative, is flexible, thrives in a dynamic environment and has a passion for technology and problem solving. You are a brilliant communicator who collaborates easily with different types of people and has a strong ability to understand and meet customer needs. We also value that you have a genuine interest in quality assurance and that you are driven by challenges and personal development. Work-life balance is important to us, and we strive to create an inclusive work environment where you can grow and thrive.
We are looking for people who:
- Has extensive experience in the development and regulatory work of medical device software (stand-alone software, embedded medical device software or of computerized support systems within medical device companies).
- Preferably with experience in the following: (MDR/IVDR, ISO 13485, IEC 62304, IEC 82306, ISO 14971, IEC 62366, MDSAP audits and FDA applications).
- Is structured and goal-oriented with a good ability to handle complex tasks.
- Is proactive and flexible, and can adapt to changing conditions.
- You have a large network within the industry and have built long-term relationships. Have a strong ability to lead and develop both yourself and others.
- Communicates effectively and collaborates easily with colleagues and customers.
- Is genuinely interested in technology, problem solving and improving processes.
Being part of Team PV
We are very proud to be a certified Great Place To Work company, which places us among the best employers in Sweden. The fact that we are also on the top list of Sweden's Best Workplaces is proof that together we have succeeded, and continue to succeed, in creating a fantastic culture.
We are not like everyone else - we are unique with our deep skills and industry knowledge combined with our warm passion and community that cares for each individual. We are a workplace that is more than just the job. And the key is we who work here. We have an extraordinary commitment and love to share our brilliant ideas. We go into what we believe in, and we do it wholeheartedly. We have the energy of a small company combined with the calmness only a company with our long experience can feel. We want to develop. We want to move forward. Together for a better tomorrow, that's Team PV.
Application
If you think we are the right place for you and that you are the right person for us, send us your application today! Selection will take place on a rolling basis. Start date is by agreement.
If you have any questions about this position, please contact Sara Kyrkander on 073-08619 48 or sara.kyrkander@plantvision.se.
