Quality Assurance Specialist to Global Medtech company in Lund!

Do you have a passion for creating structure in an innovative environment? Do you get a kick from running projects and tasks independently? Do you have previous experience of QA work and have a passion for ensuring that the quality work complies with laws and regulations? The QA-team at CellaVision is now looking for an experienced Quality Assurance Specialist!


As a Quality Assurance Specialist your main task is to ensure that CellaVision complies with laws and regulations. You will be part of an experienced team of three colleagues and report to the QA Manager.

What you will do as a Quality Assurance Specialist at CellaVision:

  • Non-conformity investigations
  • Product care - quality work
  • Release of systems / products
  • Change Management
  • Monitor and initiate updating of quality routines
  • Complaint investigations
  • CAPA investigations
  • Internal Auditor
  • Handle quality issues to suppliers
  • Other tasks at CellaVision’ s QA department

Who we are

CellaVision is an innovative, global med tech company that develops and sells its own leading systems for routine analysis of blood and other body fluids in health care services. Our headquarter is in Lund, Sweden where we are a QA department of in total 10 persons within Quality Assurance, Clinical Affairs and Regulatory Affairs. We have the superpowers to support the global CellaVision organization of 180 employees covering 32 countries. In 2019, sales were SEK 462 million and the company's growth target is 15 % per year over an economic cycle. The share is listed on the Nasdaq Stockholm, Mid Cap list.

Who you are

You have a well-developed ability to review complex tasks and prioritize them at a high pace. You work with integrity and take responsibility for your own tasks in both success and setbacks. You work independently and we believe you appreciate being part of a team where you work together and share information and solutions. Finally, we believe that with experience comes personal growth. You understand the importance of putting effort into your work and acting as an example to follow.


  • MSc or equivalent in the relevant field
  • Several years of experience in qualified QA work with similar tasks within Med tech or pharmaceuticals 
  • Knowledge in QSR (21CFR 820)
  • ISO 13485
  • Excellent written and verbal communication skills in English and Swedish

If you also have good knowledge of ISO 14001 this is considered an advantage.

Care to join?

Submit your application including CV and attachment letter. We will work with continuous selection and interviews, so please send your application as soon as possible. We do not accept applications via email.

This is a full-time position with start as soon as possible, based at CellaVision HQ in Lund, Sweden with new offices, good infrastructure and commuting possibilities.

Note that you need a valid working permit in Sweden.

To know more about the position, please contact recruiting manager Nina Wallin Carlquist, Quality Assurance Manager, at nina.carlquist@cellavision.se

Questions about the recruitment process contact Caroline Herrlander, HR Specialist, at caroline.herrlander@cellavision.se.


We decline all contact regarding services in advertising, consulting or recruitment.


Or, know someone who would be a perfect fit? Let them know!

Some of your colleagues

CellaVision Headquarter

Mobilvägen 12
223 62 Lund Directions View page

Workplace & Culture

The corporate culture here at CellaVision is based on openness, teamwork and creativity. We set high personal development, and we give our employees the opportunity to shape their role and their work situation.

Besides having fun together during working hours, we make sure we come out on common activities and thus grow together. We are proud of our corporate culture and every day we strive towards building strong, collaborative teams, and creating an inspiring place to work at. 

Already working at CellaVision?

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