Regional Quality and Regulatory Affairs Specialist

Job description
You will be providing support, training and advice to the business and operations through active participation
You keeps track of the regional mandatory audit schedules and the related "Global Linde standards" Region Europe North (REN) ISO certifications (ex. ISO9001, ISO14001s as well as relevant Global standards and EU-regulations - for our medical products and medical devices
You also train and audit the regional business units on GxP requirements
Monitor, analyze and follow-up on Quality performance and compliance, of medical products and medical devices
Participate and/or lead several internal GxP and pharma audits
You have a good contact with our notified bodies for a continuous update on changes of legal requirements, assure a smooth maintenance of our quality management system and product certifications



Qualifications
You have a good knowledge about Quality demands related to medical products
At least three years of Operational experience from the pharmaceutical and/or chemical industry
You have a degree/knowledge in Pharmaceutical science and/or Chemistry
Being driven, supportive, organized and analytical
You have good communication and presentation skills
Active partner in team work across national borders
Excellent written and verbal communication skills in English is a must, any additional Nordic language is a benefit