Quality Assurance Specialist to Global Medtech company in Lund!

The Quality Assurance team

You will be a key part in the Quality Assurance team, consisting of two QA Specialists Anna and Jessica and our QA Manager Nina. Together they make sure that CellaVision’s quality work complies with laws and regulations. This position offers a unique opportunity to run projects and tasks independently and to plan your activities with a great amount of freedom. You will work in close collaboration with your team and be encouraged to bring new ideas to the table to drive change. Thus, this will be a broad role where you will benefit from your previous background within QA and have room to grow and be challenged.

The Quality department has in total 9 dedicated colleagues that are all passionate about creating the best quality standard in the business.  The Quality department is divided into three different functions; Quality Assurance, Regulatory Affairs and Clinical Affairs and have superpowers to support the global CellaVision organization of 180 employees covering 32 countries.

 

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 auditing
  • Handle quality issues to suppliers
  • Other tasks at CellaVision’ s QA department

 

What can we offer you?

CellaVision has a world-leading position in digital cell morphology and we see our employees as our primary resource for our ongoing innovation and success. Joining CellaVision means that you will surround yourself with over 100 passionate and ambitious colleagues, and that you will be part of developing products that do not only help patients worldwide, but also contribute to reduced environmental impact through more efficient workflows in and between laboratories.

 

Other great things with working at CellaVision are:

  • We have a friendly and open company culture in a flat organization.
  • We have a modern office to boost cooperation as well as the ability to work undisturbed.
  • You will get a yearly wellness grant and free access to the gym.
  • You can take part in social events such as the weekly running group, board game evenings, Cella Choir, etc.
  • You will get an extensive onboarding package for new employees including a visit to the lab to see our products live and an assigned mentor.
  • We have flexible hours to promote work-life balance.
  • You can take part in “Meet-n-eat” lunches where you get to meet new colleagues every month.
  • We have collective agreements, ITP-pension, parental leave supplement, reduction of work hours etc. 

Who you are   

You have a MSc or equivalent in the relevant field as well as several years of experience in qualified QA work with similar tasks within Med tech or pharmaceuticals. You have a passion for creating structure in an innovative environment and get a kick from running projects and tasks independently. You have knowledge within QSR (21CFR 820) and ISO 13485 and express yourself excellently in English and Swedish (written and verbal). If you also have good knowledge within ISO 14001 - you might be the perfect match! 

 

Because the QA team is a small team, we give our colleagues both a lot of freedom but also a lot of responsibility when it comes to independent work and owning your tasks in both success and setbacks. We apply an open climate and have a close collaboration between departments, so your ability to cooperate is something we value highly. We believe you have a well-developed ability to review complex tasks and are used to prioritizing them. We believe you appreciate being part of a team where we work together and share information and solutions. We also believe you are a meticulous person who organize and prioritize your work efficiently and who is passionate about presenting high quality work. Finally, you enjoy an innovative environment, where no week is like the week before and laughter and small talk is never far away.

 

Are you ready to make a difference? 

Join CellaVision, put your quality skills to greater use and help us contribute to lab efficiency and improved patient value worldwide. We need your expertise to do the job!

Apply to this job by filling in the application form and attach your CV/personal letter. Please prepare to have your documents, such as certificates, credentials and recommendations, for a potential interview. We review applications continuously, so please send us yours as soon as possible.

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. To know more about the position contact Nina Wallin Carlquist, QA Manager, at nina.carlquist@cellavision.com. Questions about the recruitment process are answered by Caroline Herrlander, HR Specialist, at caroline.herrlander@cellavision.se. We do not accept applications via email.

 

Please note that you need a valid working permit in Sweden for this role.

We respectfully decline all contacts regarding additional channels, campaigns or recruitment support.

 

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

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?

Let’s recruit together and find your next colleague.

email
@cellavision.com
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