Quality Assurance Professional


We are looking for a Quality Assurance Professional who will act as a strong player in a flexible and dedicated QA team.

Are you passionate about quality management and process development? Do you want to drive improvements and support the business area in ensuring effective ways of working? If so, this role might be something for you.

Location: Malmö

Last day of application:  15 March 2020.

ROI is responsible for this recruitment, please send your CV and application letter thru link below. We advise you to apply as soon as possible as we review and interview continuously. All applications are treated confidentially. 

For questions:
Please contact My Tran, QA/RA, tel: +46 72 08 07 003, email: my.tran@svarlifescience.com

Download Job Description - Quality Assurance Professional

Please respect that we are not interested in offers of advertisement or recruitment assistance.

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We are looking for a Quality Assurance Professional who will act as a strong player in a flexible and dedicated QA team.

We have high ambitions of delivering excellent customer service and support to both our customers and throughout the Svar organisation.

Work is governed by regulations such as ISO13485, GLP, ISO1518 and 21CFR820.


Some of the main task in our QA/RA team include but are not limited to:

  • Review and approve quality documents, such as SOP´s, validations and test methods etc.
  • Conducting internal quality audits and contribute at external audits/inspections.
  • Develop and drive improvement of the Quality Management System
  • Keep up to date regarding current industry regulations/guidelines.
  • Participate in projects as quality representative.
  • Support QMS processes with investigations and approvals to ensure quality compliance.


The successful candidate should ideally have some years of experience within QA or Regulatory Affairs from medical device or the pharmaceutical industry. The candidate holds a strong willingness to learn and develop within the profession, with an analytical and problem-solving mindset. Are you furthermore excited about coaching and developing a dedicated team and support them in their role to ensure ambitious department- and cooperate goals this would be meritorious.

  • Demonstrate good communications skills, social adaptability and humility.
  • You must enjoy trying new approaches and being prepared to try new tasks.
  • Excellent written and verbal communication skills both in Swedish and English.
  • Bachelor’s Degree in chemical engineering, chemistry, biochemistry or equivalent.
  • Experience within ISO 13485, MEDDEV, CFR regulations, GLP and GCP etc.
  • Experience within regulatory affairs is an advantage.
  • Experience from project management or team management will be considered a plus.