Om jobbet
Job DescriptionQARA PD Director WC
Lead change that lasts
At Mölnlycke, we believe that real impact starts with people. People who are bold enough to challenge the status quo. People who care deeply about their work, their teams, and the patients they ultimately serve.
As a global medical solutions company, we develop innovative products and solutions that improve outcomes and advance performance in healthcare worldwide. In Wound Care at Mölnlycke, we help to prevent, manage and accelerate the healing of wounds.
Why This Role Matters
This is more than a leadership role, it's a transformation opportunity. In this role, you'll play a key part in shaping how we work, not just what we deliver.
As QARA Product Development Director for Wound Care, you will lead a newly integrated QA and Regulatory Affairs organisation, shaping how teams collaborate, operate, and deliver value across the product lifecycle.
You will be at the forefront of driving change, building engagement, and ensuring that our organisation is set up to meet both current and future regulatory and quality demands.
How You'll Make an Impact
Lead and develop a global QA/RA Product Development team
Drive integration and alignment between Quality and Regulatory functions
Establish and embed new ways of working across product development
Provide strategic direction for regulatory and quality activities across the lifecycle
Ensure effective execution of regulatory strategies and submissions
Partner cross-functionally with R&D and business stakeholders
Build a strong, engaged, and high-performing team environment
Identify and mitigate regulatory and quality risks proactively
Contribute to broader QARA and business strategy execution
What You'll Get
A leadership role with real organisational impact
Opportunity to shape and lead transformation at scale
A collaborative, purpose-driven global environment
Career growth within a leading global healthcare company
Flexible working approach (with HQ presence initially expected)
Competitive compensation and benefits
What You Bring
Must-Haves
Strong leadership experience in QA/RA (min 7 yrs) within medical devices (min 10 yrs)
Proven track record in leading organisational change or transformation
Cross-functional facilitation skills
Experience leading and developing global teams
Solid understanding of both Quality and Regulatory frameworks
Strong stakeholder management and influencing skills
Nice-to-Haves
Experience within product development environments
Deep expertise in regulatory strategy and submissions
Experience working across global regulatory environments (EU, US, UK)
Our approach to Diversity & Inclusion
We're building a workplace where everyone feels seen, heard, and valued. We believe that diverse perspectives drive better decisions and stronger outcomes, and we're committed to creating an environment where everyone can thrive.
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 four 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 worldwide. The headquarters are in Gothenburg, Sweden, and we operate in more than 100 countries.
