With a passion for life

Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers – and to save more lives, we need team players, forward thinkers, and game changers.

Are you looking for an inspiring career? You just found it.

About the role

Quality is a promise to our customers. Medical Device safety and Quality Compliance is a top priority commitment at Getinge to save lives and maintain customer trust. As a Senior QA Specialist we trust you to bring in your experience and knowledge from quality and compliance to help us improve our ways of working, leading us to better product quality and higher customer satisfaction.

Our Quality and Compliance team in Solna is team of ten people being ambassadors for the compliance to medical device regulations and ISO14001, as well as other applicable standards and regulations. The team is working in close collaboration with our quality team at our sister site in Germany.

We are responsible for preparing, hosting and responding to external audits, as well as performing supplier and internal audits. We also lead the activities related to CAPA (Corrective and Preventive Actions), Management Review and several business related improvement projects, as well as monitoring of standards and regulations. We are passionate about improvements and love to find new efficient ways of working while keeping the compliance.

Main responsibilities

• Support business improvement projects and digitalization
• Quality system support to stakeholders across the organization within Manufacturing, Design and Development, Purchasing Controls, HR, IT etc.
• Performing internal audits, identifying improvements and track nonconformances to closure
• Participate in preparation of external audits, management reviews and supporting the CAPA (Corrective and Preventive Actions) process
• Involvement in monitoring and gap assessment of new standards and regulations
• Supporting the organization with regards to quality issues and improvements of our procedures in the management system

What you bring

The person we are looking for is ideally working with development and manufacturing of medical devices today. You are used to building, implementing and maintaining procedures in a regulated industry.

We believe that your key characteristics include:

• Academic degree (M.Sc or B.Sc) in science or engineering
• At least five years, preferably 8-10 years, of working experience from a similar position
• Documented knowledge in applicable regulations and standards, such as ISO13485, QMSR, MDSAP and ISO14001
• Well-developed analytical and administrative skills
• Strong verbal and written communications skills in Swedish and English
• Good track record of communication in cross-functional work, preferably in global organization
• Experience from product development and/or software tool implementation is beneficial
   

Being able to communicate efficiently with different stakeholders, on all levels and from different cultures, in a professional and diplomatic manner, is important in order to succeed in the role.

As a person you are a result-oriented and collaborative team-player who drives results, takes responsibility with ability to work independently. You have an analytical and pragmatic mindset.

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.

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 Katarina Blomberg at email: Katarina.blomberg@getinge.com or Recruiter at emma.paulsson@getinge.com

About us 

With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.  

Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process. 

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