Arbetsbeskrivning

About this opportunity

Welcome to our Getinge Disinfection site in Växjö, where we manufacture washer-disinfectors and endoscope reprocessors for healthcare, meeting high standards of patient safety, functionality, and user-friendliness.

You will join our Quality team, which focuses on driving continuous improvement and ensuring compliance with quality standards across our operations. The team collaborates closely with cross-functional stakeholders to enhance processes, workflows, and services, contributing to Getinge’s mission of delivering high-quality products and solutions.

In this role, your will have the primary responsibility for the support and coordination of the Quality systems to improve and secure the regulatory compliance for Document control and Document implementation.

What you will do

• Coordinate local implementation, according to timeline, of updated global policies, directives and standard operating procedures (SOP).
• Support and coordinator (Gate keeper) of the digital document- and quality management system to ensure correct update and implementation of processes and work instructions.
• Introduce employees in basic quality training, document handling system and publication platform
• Supporting management in Management review process
• Be involved in quality plans when changes affecting QMS
• Review and compilation of documents.
• Initiate and drive improvements within the department.
• Involved in activities for external and internal audits
• Responsible for the publication platform for QMS

This position is based in Växjö and the position is eligible for a hybrid setup with 1-2 days working from home.

You will bring

To be successful in this position, we believe that you have the following qualifications.

• Bachelor’s degree in Quality Assurance or Engineer graduated in a technical area or equal.
• Minimum 3 years experience in a Medical Device manufacturing environment or equal.
• Excellent communication skills and strong written skills.
• Excellent working knowledge of MS Office (Word/Excel) and a statistical based software package.
• Good Swedish and English skills, oral and written
• Analytical competence

• Experience and knowledge in applicable regulations and standards, e.g. ISO 14001, ISO 13485, ISO 14971, MDR, MDD and MDSAP is meritous.

In addition to your technical skills, we highly value your personality. We think you are a team player with the ability to work in cross-functional teams. You are also used to work independently and being able to make decisions within your scope. In addition to this we think you have good communication skills and excellent structure in your daily work.

At Getinge we see ourselves as proactive and self-driven in learning and contributing to the continued development of our products and our organization's capabilities. We are Team Players, Forward Thinkers and Game Changers.

We think you will thrive in a high-expectation environment and have an interest in our products.

Why join Getinge

Getinge offers a job in a safe and informal work environment, where we appreciate close team collaboration. We keep an open dialogue between leaders and employees, as well as between teams. We are focused on developing people, and together we will create a plan for learning and competence development when you start your career with us.

We offer a competitive compensation and benefits package, including wellness allowances, generous family benefits and joint company activities. Everything to ensure we support your well-being and goals.

Application

Applications will be reviewed continually, and we therefore recommend sending us your application as soon as possible, but no later than 2026-05-01

We kindly ask you to submit your application in our recruitment system by clicking the “apply now” button. Due to GDPR regulations we do not accept applications via e-mail.

If you have any questions regarding the role, please contact Hiring Manager Nina Stewén at email: nina.stewé[email protected] or Recruiter at [email protected]

We look forward to receiving your application. We hope you will join us on our journey to become the world’s most desired MedTech company.