Clinical Compliance Coordinator

 

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 fixed-term opportunity (approximately 12 months, from July 2026) to cover a maternity leave within our Clinical, Medical and Professional Affairs department.

 

Why This Role Matters

Mölnlycke is now looking for a Clinical Compliance Coordinator to join the CMPA team on a fixed-term basis- offering a unique opportunity to play a critical role in advancing clinical compliance within a global MedTech leader.

 

This role goes beyond traditional coordination. You will work closely with experienced professionals across Clinical, Medical and Professional Affairs, and other functions, supporting the effective execution of clinical compliance processes that underpin high-quality evidence generation, dissemination, and patient safety.

 

As part of a global team, you will play a key role in ensuring that clinical compliance activities, systems, and documentation are well-coordinated, audit-ready, and consistently applied across the organisation. This is an excellent opportunity to build deep expertise in clinical compliance operations and gain exposure to cross-functional ways of working.

 

Here's how you'll make an impact:

• Support the execution of clinical compliance operations and initiatives, ensuring consistency and quality across business areas
• Coordinate and develop clinical compliance training initiatives, including e-learning modules, in collaboration with relevant stakeholders
• Manage document review, routing, and release processes within validated digital quality systems (e.g., MasterControl) across all business areas
• Support Healthcare Professional (HCP) engagement processes, including implementation and delivery of required compliance trainings
• Assist with audit-related activities, including preparation, participation, and follow-up (e.g. supplier qualification and study audits)
• Provide administrative coordination and documentation support for site-facing evidence generation activities (e.g., Investigator-Initiated Studies [IIS], Quality Improvement Projects [QIP]) under the oversight of designated process owners
• Maintain the department's digital document repository and clinical compliance infrastructure, ensuring documentation is accurate, audit-ready, well-organised, and up to date Support the roll-out of new processes, systems, and regulatory updates ensuring clear communication and adoption
• Contribute to the institutionalisation of clinical compliance knowledge, supporting sustainable documentation practices and long-term knowledge management

 

What You’ll Get

Your growth and development

You’ll gain hands-on experience in a highly regulated, globally operating medical device company, working at the intersection of clinical compliance, digital operations, and cross-functional coordination. This is an opportunity to build expertise that matters, in a company that is clear on its mission and bold in its ambitions.

• Exposure to global clinical compliance practices across multiple business areas
• Engage and collaborate with experienced professionals across Clinical, Medical and Professional Affairs, Regulatory, Quality, and other global support functions, driving cross-functional alignment and exchange of expertise
• Fixed-term contract of approximately 12 months from July 2026

 

 

What You Bring

We're looking for someone who is digitally confident, highly organised, and thrives in a fast-moving, regulated environment. If you bring the right mindset and coordinating experience, especially from healthcare or life sciences, we encourage you to apply.

 

Must-haves:

• Experience in coordination role, ideally within the healthcare, life sciences, or medical device industry (backgrounds study coordination, clinical affairs, or research coordination are highly relevant)
• Strong digital literacy, confident working with digital tools, document management systems (e.g. Master Control), and Microsoft Office (especially PowerPoint and Excel)
• Ability to maintain and present information clearly, with a flair for good visuals and structured communication
• Strong organisational skills with attention to detail and a continuous improvement mindset
• Strong written and verbal communication skills in English
• Ability to adapt quickly to new systems and ways of working; resilience and flexibility are essential in this environment
• A collaborative and service-minded team player with the ability to manage multiple priorities under tight deadlines

 

Nice-to-haves:

• Experience with compliance management systems or regulated document management platforms
• Exposure to site-facing (investigator/site-based) evidence generation activities (e.g., IIS, QIP) or clinical study administration
• Background in developing training content or e-learning modules
• Project management experience would be a plus
• Familiarity with EU MDR or other medical device regulatory frameworks is an advantage

 

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