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R&D Engineer-TPM

Wellspect Healthcare, with headquarters in Mölndal, Sweden, is a leading global provider of innovative medical devices with a focus on helping people suffering from urinary retention or chronic constipation. Every day, more than 1 100 employees are dedicated to make a difference for those who need our products and services. Many of the people we serve have a spinal cord injury, enlarged prostate, spina bifida or multiple sclerosis. We are one of the world’s leading manufacturers of intermittent urinary catheters, with LoFric® as our most known brand. As a help to those with chronic or severe constipation we have developed what likely is the world’s most advanced irrigation system, the Navina Systems™, combining a high degree of user convenience, clinical effectiveness and connectivity into one really smart system. Wellspect HealthCare has a presence in more than 30 countries, and is a part of Dentsply Sirona, the worlds´ largest manufacturer of professional dental products and technologies with global headquarters in York, Pennsylvania, and international headquarters in Salzburg, Austria. 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.”

We offer

Join our team as R&D engineer-TPM where we challenge and explore new ways in our effort to continuously improve ourselves, individually and as a team. A great opportunity if you want to work in a successful company with products that makes a real difference.

About the position

As a Technical Product Manager you will be responsible for structuring the work flow of non-disposable product with electronic devices with version updates. You will also be involved in development of new and improved products, with focus on electronic systems.

Your key accountabilities are

  • Changes in design and materials, both new and existing assortment.
  • Develop product documentation in compliance with regulatory requirements, Medical Device Directive, FDA and internal Quality Management Systems.
  • Development activities in various stages in cross-functional projects.

It is also considered an advantage if you are familiar with ISO 13485 FDA Quality System Regulation or have experience from medical device or other product areas with high regulatory demands.

Who you are

We think you are a positive and structured team player that is motivated by problem solving. You are open for challenges and enjoy working together with highly skilled and committed colleagues.

We believe you have

  • An academic background, preferably in Electronic engineering.
  • Some years of experience in R&D -TPM.
  • Excellent documentation and communication skills, both English and Swedish. 

In this recruitment we are cooperating with K2 Search. For further information about the role please contact Lena Serner, tel. 0702-900 995 or Jon Spjuth tel. 0765-253 852. All applications and contacts remain confidential. Selection is ongoing so do not wait to submit your application. Please submit your application on www.k2search.se