Elekta is proud to be the leading innovator of equipment and software used to improve, prolong and save the lives of people with cancer and brain disorders. Our advanced, effective solutions are created in collaboration with customers, and more than 6,000 hospitals worldwide rely on Elekta technology. Our treatment solutions and oncology informatics portfolios are designed to enhance the delivery of radiation therapy, radiosurgery and brachytherapy, and to drive cost efficiency in clinical workflows. Elekta employs 3,600 people around the world. Headquartered in Stockholm, Sweden, Elekta is listed on NASDAQ Stockholm. www.elekta.com.

Quality Assurance Specialist

Elekta is now looking for a Quality Assurance Specialist to fill an interesting role in the organization. This opportunity is well suited for a person who wants to improve, support and drive quality system processes and related governance activities.

The Role

Your key responsibilities will be following:

  • Support the implementation of Elekta Quality Policy, other directives and processes throughout the Elekta Solutions quality system and organization
  • Promote the quality system and its principles throughout the organization.
  • Suggest and implement quality related process improvements
  • Quality KPI monitoring and gathering 
  • Manage and perform internal audits
  • Support external audits preparations and participate
  • Support quality system non-conformities handling including local CAPAs
  • Training of the organization in the quality system.
  • Support activities/projects in accordance with the RA & Q overall business plan and in alignment with the overall business objective

The role is in Elektas head office in Stockholm. 

Elekta can offer you a global environment where quality assurance is highly valued. You will be a part of a motivated team where you will have the ability to influence the development of the company as well as your own career. 

Background and personal qualities

To be successful in this role you need to have a university degree from a pertinent field such as mechanical, industrial, electrical engineering or equivalent area. You also have experience from quality work within the medical device industry. You have performed internal audits and are acquainted with external audits. You have a good knowledge of the European Regulations for Medical Devices (MDD/MDR), MDSAP, US FDA legislation and related harmonized ISO standards. Experience from acting in a global organization or within design and manufacture would be of advantage.

You have excellent English, both orally and written.

Highly valued personal qualifications and competencies are as following: 

  • Confident and open personality who can communicate effectively, both written and orally with people at all levels
  • Administrative skills and capable of producing results working unsupervised under own initiative
  • A structured/organized approach to problem solving with an appreciation of quality tools & techniques
  • An effective team player who prefers to share and communicate problems and solutions with other members of the team
  • Confident and open personality who can communicate effectively, both written and orally with people at all levels
  • A positive attitude towards change to promote the global goals of the business.

Application

In this process Elekta is working with Level Recruitment. To apply, please visit www.levelrecruitment.se and click on “Ansök här”. If you have any questions please contact Louisa Torstensson at 08-120 50 423.