Vill du vara med och kommersialisera en tjänst som både kan förbättra och effektivisera dagens hälso- och sjukvård?

Nu söker vi någon som kan stärka upp teamet med fokus på kvalitetssäkring. Vi söker dig som vill vara med och spela en viktig roll i arbetet med implementering, underhåll och vidareutvecklingen av Hemchecks kvalitetsstyrningssystem. I tillägg finns möjlighet att forma tjänsten utifrån sökandes kompetenser då Hemcheck också har behov av tex. klinisk kompetens, utvecklingskompetens, mm. Kandidater behöver inte ha arbetat inom QA tidigare och kommer i så fall att få utbildning inom det området av Hemcheck.

Läs mer och välkommen med din ansökan!

The company:
Hemcheck Sweden AB Hemcheck was founded in 2010 with the vision of addressing the most common reason, hemolysis, for blood samples not being suitable for analysis. Hemolysis, the rupturing of red blood cells is a global problem that creates a lot of issues for the healthcare systems since the analytical results from analysis of hemolyzed blood samples are distorted and blood samples need to be redrawn in order to correctly analyze patient blood. Hemcheck is producing and selling a simple, yet sophisticated service addressing the issue of hemolyzed blood samples, at the point of care. The service consists of a product concept of single use point of care tests, a reader as well as training to medical staff. The concept enables healthcare staff to directly at the patient side detect hemolyzed blood samples and redraw the blood without leaving the patient. This will reduce waste, improve lead times, improve patient safety and healthcare quality while reducing overall costs. We are an innovative company addressing a new solution to a well-known problem. Hemcheck is listed at Nasdaq First North Growth Market and is based in Karlstad, Sweden. Additional company information is available at www.hemcheck.com.

The position:
As Hemcheck is launching its service in the market, it is of great importance for the company to have a complete quality management system in place that is in regulatory compliance. We have in place a quality management system and we now look forward to strengthening the company with someone that can take responsibility for our quality assurance activities going forward in addition to supporting other processes such as sales, R&D and clinical implementation. The position can be tailored to a candidate’s specific competence profile and training in QA will be provided as needed. We search for a candidate that wants to play an important role in our company by taking responsibility for the further implementation, maintenance and development of Hemcheck´s quality management system as well as contributing in other areas.

The main responsibilities as a Quality Assurance Manager at Hemcheck will cover:

• Development and implementation of regulatory strategies
• Further development and implementation of our quality management system and product files (Processes and Procedures, such as risk analysis, validation, change control, CAPA, Post-Market Surveillance, writing and reviewing SOPs and other quality-related documents).
• Maintenance of existing quality management system and product files
• Monitoring and interpretation of legislations, standards and guidance
• Support the regulatory processes related to new market entries and new product launches

In addition, there will be additional responsibilities to support in other important areas. We will form the role to the specific candidate’s competence profile.

Qualifications:
You preferably have previous experience in working in the medical devices industry or in a clinical setting (e.g. nurse or BMA). Previous experience of work within the field of Quality Assurance is a plus but not a requirement. You can express yourself in both Swedish and English, both orally and in writing. You are expected to be able to independently plan and run your daily work while being a team player and have a positive attitude towards work and colleagues. You also need a systematic approach combined with an analytical ability as well as being open for new challenges in an entrepreneurial environment. Great emphasis is placed on personal suitability. Your professional skills preferably include:

• A university degree on bachelor or master level
• Experience in project management
• Experience from the medical devices industry or a clinical setting
• Knowledge for standards for quality management system and risk management for medical devices, especially ISO 13485 and ISO 14971

Interviews will be held as soon as relevant candidates have been identified. Please send your application to joen.averstad@hemcheck.com.

We offer:

Hemcheck is an innovative growing company that offers You to take part in an interesting journey from development to production to product launch and market introduction of a unique patented solution. Being a team member of a smaller company You will be involved in all the regulatory steps and have full insight in the regulatory processes, as well as support other processes such as R&D.