AdressJob 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
