Make your next move matter
At Mölnlycke, we believe that real impact starts with people. People who are bold enough to challenge the status quo. People who care deeply for their work, their colleagues, and the world around them. People who know exactly why they do what they do.
As a global medical solutions company, we design and deliver innovative products and services across wound care, operating room solutions, gloves, and antiseptics. Our mission is to advance performance in healthcare by supporting professionals, improving outcomes, and making a difference where it matters most.
This is a temporary opportunity to support our team during a period of parental leave. You’ll bring your expertise to a team that values clarity, accountability, and collaboration. Your work will help us move forward efficiently and effectively.
In Wound Care at Mölnlycke, we help to prevent, manage and accelerate the healing of wounds.
Why This Role Matters
This isn’t just a job, it’s a chance to be part of something bigger. You’ll join a global team with a shared mission: to advance performance in healthcare.
Here’s how your contributions will shape meaningful outcomes:
Plan and deliver post-market surveillance activities (PMS, PMCF, PSUR, SSCP), ensuring compliance and continuous improvement
Coordinate documentation to support international market approvals (e.g. CFS, regulatory statements)
Execute and document method validations to meet quality and regulatory standards
Analyse quality and environmental trends, driving corrective and preventive actions
Coordinate biocompatibility studies in line with ISO 10993 and maintain up-to-date documentation
Maintain risk management activities in accordance with ISO 14971 across the product lifecycle
Develop and maintain quality documentation, and support training across processes and procedures
What you bring
Fluent in German (written & spoken)
Degree in a relevant field (e.g. science or engineering)
3+ years’ experience in QA, RA, or R&D within a regulated environment
Hands-on experience with quality management systems and controlled documentation
Experience with method validation (and/or qualification activities)
Strong analytical skills with a structured, detail-oriented approach and ability to meet deadlines
Experience in the medical device sector, including post-market requirements or regulatory processes is desirable
Knowledge of biocompatibility or risk management standards (e.g. ISO 10993, ISO 14971) would be advantageous
What you’ll get
Be part of a culture built on trust, care, and shared ownership.
Flexibility, wellbeing and benefits that reflect our commitment to you.
Fixed term – 18 months
May be eligible for annual bonus up to 5%
25 vacation days per year plus public holidays
Wellbeing initiatives
Details about this job
Full Time (Permanent employment)
- Monday to Friday
- 38,5 hours
Place of work
- Salzburg (Stadt)
Must-have skills
- Quality Assurance
- Regulatory Affairs
- Risk Management
- Document Control
- Internal Auditing
Must-have education
- Degree in a relevant field
Details about this job
Full Time (Permanent employment)
- Monday to Friday
- 38,5 hours
Place of work
- Salzburg (Stadt)
Must-have skills
- Quality Assurance
- Regulatory Affairs
- Risk Management
- Document Control
- Internal Auditing
Must-have education
- Degree in a relevant field
Our approach to Diversity & Inclusion
We’re building a workplace where everyone feels seen, heard, and valued. We believe that a diverse mix of people (from different cultures, ages, geographies, and genders) makes us stronger. It brings fresh perspectives, drives better decisions, and helps us deliver solutions that reflect the world we serve.
Inclusion isn’t just a value, it’s how we work, grow, and lead together.
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 GoCo Health Innovation City, a world-class innovation cluster for health.
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
