Quality Manager
Date: Feb 27, 2026
Location: Molndal, SE, NA
Company: Dentsply Sirona, Inc
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Requistion ID: 82358
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Wellspect Healthcare is a leading global provider of innovative medical devices that help people suffering from urinary retention or chronic constipation. More than 1 000 employees around the world are dedicated to making a difference to people who need our products and services. Wellspect is one of the worlds’ leading manufacturers of intermittent urinary catheters, with LoFric® as the most known brand. As a help to those with chronic or severe constipation Wellspect has developed what likely is the world’s most advanced irrigation system, Navina™, combining a high degree of user convenience, clinical effectiveness and connectivity into one smart system. Wellspect strives to become climate neutral and leave the smallest possible environmental footprint. The company, with headquarters in Mölndal, Sweden, is present in more than 30 countries, and part of Dentsply Sirona, the worlds´ largest manufacturer of professional dental technologies. The company’s shares are listed in the United States on NASDAQ under the symbol XRAY. Visit www.wellspect.com and www.dentsplysirona.com for more information.
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Quality Manager
Do you want to be part of a skilled and dedicated team, contributing to keeping our product safe and of high quality while also having fun at work? Join our team to make a real difference!
In this position, you will work within our Quality Assurance department, supporting both existing products and new development projects. You will collaborate closely with cross-functional teams and have the opportunity to contribute to the development of our new products. You will also act as a process owner and provide support to colleagues across the organization.
Responsibilities:
- Review and release of batch documentation
- Manage non-conformities
- Review and approve change notifications
- Provide QA support for products and development projects
- Participating in validation activities
- Lead the CAPA Process and facilitate root cause investigations
- Perform Process and System Improvements
- Conduct Post Market Surveillance
Background/Qualifications
- Master´s or Bachelor´s degree in engineering, science, or a technical field.
- At least 5-10 years of experience within Quality Assurance
- Experience of working within Medical Device Industry and have knowledge about ISO 13485 and 21 CFR Part 820.
- Strong drive to achieve goals and deliver results
- Solid documentation and communication skills in English, and the ability to communicate in Swedish
Who you are?
We think you are a positive and social team player with the ability to maintain good relations with both external and internal contacts. You are open to challenges and enjoy working together with highly skilled and committed colleagues. You have high integrity and a strong performance drive as well as a wish to look into new ways of working. If you have worked as a Lead Auditor and/or have good knowledge in the statistical area this is an advantage.
We can offer you an exciting and challenging job in a company that is committed to make a real difference every day. This position is located at our headquarter in Mölndal, Sweden.
We will evaluate CVs on a frequent basis so please send in your application asap.
We look forward to hearing from you!
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