Alla uppdrag
Program Manager Notified Body
quality management, regulatory affairs

Vill du ha stort ansvar? Har du arbetat länge inom regulatory och har god kunskap om filgranskning och auditprocessen? Har du även kunskap inom MDD. Kontakta mig för att få veta mer om denna tjänst.

At least 3 years’ experience in the medical-technical industry e.g. within auditing, quality management, regulatory affairs, research & development or production/service.
Experience in one or more of the following is a distinct advantage:
• Medical Device Directive
• Sterile
• Technical File Review
• Auditing
• Medical-technical industry
• Dental or implantable devices
• Health care
• Risk management
• Scientific literature or clinical trials
• Medical device regulations
• Industry practice and standards

Higher education, MSc, and/or equivalent experience in either Health Science, Engineering or Quality/Regulatory disciplines related to the Medical Device or Pharma industry sectors.

Personal competencies
As a person you are independent, organised, analytical, thorough and results-oriented. You have a keen eye for detail but can also take a step back to see the bigger picture when required. You are able to react effectively in stressful situations, have strong communication and interpersonal skills and the ability to define problems, collect data, establish facts and draw valid conclusions. Effective time management is also essential to the role.
Lastly, you have good working knowledge of Office systems, and speak and write Swedish and English fluently.

Vill du veta mer, kontakta ansvarig konsult för denna rekrytering Erik Düring. Rekryteringskonsult på Rekryteringsspecialisten AB.

Kontaktuppgifter: mobil 0708 999 469