Join us and make a difference
If you’re ready to have an impact in a career that makes a difference, Mölnlycke could be your next step. You’ll be helping to equip medical professionals around the world with solutions to improve outcomes for patients. And you’ll be developing yourself in a global environment with an inspirational culture, with lots of opportunities. All the while building a successful career, with real purpose.

About the Job
Are you ready to challenge yourself in a new environment and have a real impact? Mölnlycke is now looking for a Quality Systems Associate to join our team in Göteborg.
As a Quality Systems Associate, you’ll play a crucial role in maintaining the Quality Management System for our Global/Göteborg site, with a primary focus on the Document Management System, Records Management, and the Training Program. You’ll ensure that critical documents are managed efficiently, and that compliance training is effectively issued across the organization.


Your role is pivotal in supporting the Quality Management System. You’ll help guide and shape our Document Management System, ensuring that documents are created, revised, and obsoleted effectively, maintaining full traceability throughout the process. You will also manage and maintain our HQ hardcopy document archive room, coordinating all records entering and exiting the archive, and ensure that document and training materials align with our compliance standards.

Within this role you will also be issuing trainings, scheduling training classes/items and track training completions.

You’ll collaborate with a multi-functional team and have the opportunity to make a significant impact by supporting quality improvement projects and providing back-room support during internal and external inspections/audits.

Your Growth and Development
You’ll receive the support you need to develop as we continue to grow. Mölnlycke values training, and you’ll have opportunities to stretch yourself and develop new skills. We’ll provide on-the-job training and the resources necessary for you to succeed and make a difference. You’ll be part of a committed team where your impact will be recognized, and your career ambitions realized.

Location: Göteborg, Sweden
Department: Quality Assurance
Experience:
Academic background with a minimum of 2 years of experience in document control and training within the Medical Device/Pharma or a related industry is preferred/required. Experience with Master Control Document/Records Management and i Learn Training Management electronic tools is a distinct advantage.

Ready to Apply?
If you’re excited about the opportunity to make a difference and grow your career with us, we encourage you to apply. Mölnlycke is committed to providing a supportive and challenging environment where you can thrive. Join us and be part of a company that’s making a real impact in healthcare.

Our approach to diversity and inclusion
We strive to have a diverse mix of people from different cultures, ages, geographies and genders, to reflect the world in which we operate and to facilitate innovative thinking across the business.

About Mölnlycke
Mölnlycke is a world-leading medical products and solutions company that equips healthcare professionals to achieve the best patient, clinical and economic outcomes.
Our business is organised in the four business areas Wound Care, Operating Room Solutions, Gloves and Antiseptics, where customer centricity, sustainability and digitalisation are at the heart of everything we do.
Mölnlycke employs around 8,700 people. The company headquarters are in Gothenburg, Sweden and we operate in more than 100 countries worldwide. Mölnlycke is a founding partner of Go Co Health Innovation City, a world-class innovation cluster for health, and in early 2025 our headquarters will move there.
Since 2007, the company has been part of Investor AB, an engaged owner of high-quality, global companies which was founded by the Wallenberg family in 1916. For more information, please visit www.molnlycke.com and www.molnlycke.com/careers