Hovione is a fine chemicals company dedicated to the process development and manufacture of active pharmaceutical ingredients (APIs). Serving exclusively the Pharma Industry, Hovione has 4 FDA approved plants in Europe, Asia and in NJ, USA, and is committed to the highest levels of service and quality. With 51 years experience in chemical process and 1100 m3 of reactor capacity, Hovione produces industrially more than 45 APIs.
We are looking to fill the following position at our Loures plant:
Quality Technical Expert (Qualification & Validation)
Profile:
• University degree in Chemistry, Chemical Engineering, or equivalent degree in a scientific area.
• 2 to 4 years experience in an operational area;
• Good general knowledge on Quality, cGMPs, ICH and ISO guidelines as well as experience on their application;
• Good communication skills;
• English fluency (written and oral);
• Critical and proactive personality;
• Accuracy and responsibility;
• Initiative and dynamism.
Responsibilities:
• To assure cGMP compliance before, during and after validation/qualification activities by assuring that all necessary procedures are implemented and are being followed;
• To assure that systems/processes/methods are qualified/validated according to their intended use and product requirements;
• To promote the importance of high quality levels and the importance of a continuous improvement culture in core company activities;
• To participate in the alignment and harmonization of the Qualification and Validation procedures within all Hovione sites.
• To plan and/or establish Qualification and Validation requirements for each project.
We offer:
• Full time opportunity;
• Remuneration and social benefits adjusted to the job function and matching the experience;
• Excellent work environment, with a strong focus on quality and rigor.
If you wish to apply please fill in the web application at our website: http://www.hovione.pt/carreiras/carreiras.asp.
