Senior Post Market Surveillance Specialist to Vitrolife


Vitrolife is an international medical device group. Vitrolife develops, produces and markets products for assisted reproduction. Vitrolife  has approximately 390 employees and the company’s products are sold in approximately 110 markets. The company is headquartered in Gothenburg, Sweden, and there are also offices in Australia, Belgium, China, Denmark, France, Germany, Italy, Japan, United Kingdom and USA. The Vitrolife share is listed on NASDAQ Stockholm. 

Vitrolife’s vision is to fulfil the dream of having a baby. We support our customers to achieve successful treatment outcomes by providing valued solutions and services for assisted reproduction. Together. All the Way. 

 The position  

Do you have a background in life sciences or pharma industry with experience from a similar role? Do you enjoy reading and writing? Are you detail oriented? If so, we are looking for a new colleague to join the Post-Market team. One of our responsibilities is to perform post-market surveillance of our media and disposable device products, but also clinical evaluation and periodic product safety assessment. This involves the creation of plans and compiling findings from the literature and market. Subsequent reports are then generated that will describe the safety and performance and assess the benefit-risk of our products to comply with medical device regulations. You will also support in the management of clinically generated data collected by Vitrolife.  

This is a full-time position and based in Gothenburg and you will report Post Market Manager.


  • Support in the delivery of PMS activities as mandated by the EU MDR
  • Generation of post-market activity plans and reports  
  • Clinical data collection, clinical evaluation plans and reports  
  • Documentation for clinical trials and regulatory submissions  

 Skills and qualifications  

  • Relevant Life Sciences degree (BSc, MSc or PhD) with the ability to read and then process/analyze scientific literature  
  • Minimum 3 years of experience from a similar role as a Post Market Surveillance Specialist or equal
  • Good understanding of the Medical Devices Directive and preferable experience of MDR
  • Understanding of clinical experience data such as complaints  
  • Excellent communication skills in English, both verbal and written, is required 
  • Proficient with applications such as Word, Excel and PowerPoint  
  • Experience of assisted reproduction technology or clinical data management is an advantage

Personal qualities
To be successful in this position you have excellent analytical skills and the ability to have holistic and strategic mindset, combined with high level of business understanding. You are an able team worker who takes responsibility, you are goal-oriented and have a desire to achieve constant improvement and development. Characteristics required for this position involve being highly communicative and be able to influence people on all levels in the organization. You have high skills in building relations and creating networks.

 Application and Contact

This recruitment process is being conducted in collaboration with Your Talent. Please apply at If you have any questions regarding the position or the process, please contact responsible Recruitment Consultant Johan Sjöberg 0761-709851, or Martina Träen 0722-888220 or  

The application process is ongoing, and incoming applications will be reviewed on an ongoing basis, so please apply as soon as possible.





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