Validation Engineer
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Virum
The global market for pharmaceuticals is in rapid development. To keep up with the market we are looking to strengthen our department with an experienced engineer or pharmacist. In NNE we work project-based and value close contact with our customers, so you will be working closely with our customers at their sites as well as from our HQ in Virum. As a person you have a personal drive and are passionate about your work. You have good communication skills that enable you to establish a close and constructive dialogue with colleagues and customers. You have a profound quality focus are analytic, systematic and have a creative approach towards problem solving. You have a positive mindset and you work effectively, keep your promises and learn from your mistakes.
Primary Duties and Responsibilities: We provide highly specialized consulting and engineering services by combining our experience of production processes and product development within GMP.
We work in a dynamic environment where we support our customers with
• Risk assessment of products and processes
• Equipment testing & qualification
• Equipment challenge and process validation
• Environmental monitoring
• Cleaning validation
• Implementation of Quality management systems
Our project teams are based on our global knowledge and we focus on personal development and knowledge sharing.
Required Qualifications: You hold a relevant degree within engineering or pharmacy and have app. 5 years’ experience within
• Pharmaceutical Production processes
• Quality Risk Management
• Development and execution of Environmental Monitoring Program
• Development and execution of Cleaning Validation Program
• Performance validation
• Ongoing Process Validation
• Development of production procedures
If our job opening has peaked your interest, then send us a short cover letter so we can get to know you. Please include a link to you LinkedIn profile in the cover letter.
We evaluate candidates on an ongoing basis.
If you have any questions about the job, please contact Manager Lotte Vistisen, +45 3075 8224.
Deadline of application is 3/14/2020
Primary Duties and Responsibilities: We provide highly specialized consulting and engineering services by combining our experience of production processes and product development within GMP.
We work in a dynamic environment where we support our customers with
• Risk assessment of products and processes
• Equipment testing & qualification
• Equipment challenge and process validation
• Environmental monitoring
• Cleaning validation
• Implementation of Quality management systems
Our project teams are based on our global knowledge and we focus on personal development and knowledge sharing.
Required Qualifications: You hold a relevant degree within engineering or pharmacy and have app. 5 years’ experience within
• Pharmaceutical Production processes
• Quality Risk Management
• Development and execution of Environmental Monitoring Program
• Development and execution of Cleaning Validation Program
• Performance validation
• Ongoing Process Validation
• Development of production procedures
If our job opening has peaked your interest, then send us a short cover letter so we can get to know you. Please include a link to you LinkedIn profile in the cover letter.
We evaluate candidates on an ongoing basis.
If you have any questions about the job, please contact Manager Lotte Vistisen, +45 3075 8224.
Deadline of application is 3/14/2020
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Virum.
Jobbet er oprettet på vores service den 13.2.2020, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Øvrige
- Virum
- Lørdag den 14. marts 2020
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