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US: Validation Engineer in Biotech

Date: 17-Jan-2012
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Validation Engineer III-

* Organize and conduct validations related to raw material changes in membrane and finished goods. Scope of the work will include single product changes and changes affecting a wide range of products and membranes. * Focus on understanding fundamental impact of changes and the implications to final product and customer applications as well as strict adherence to cGMP policies and practices. * The position will be required to work with a broad cross section of the population including upper management, R&D personnel, process engineers, quality engineers, technicians and operators both inside and outside the Jaffrey and Bedford plants.

* Bachelors Degree in Chemistry, Chemical or Mechanical Engineering with 5-7 years experience or Masters Degree with 2-3 years experience * Experience within a cGMP manufacturing or R&D facility * Project Management skills * Lean Six Sigma or advanced statistical skills * Scientific report writing skills * Data Analysis Skills * Excellent inter-personal skills and ability to work with others * Ability to influence in a team environment * Demonstrated leadership skills within a manufacturing or scientific organization * Software: Microsoft Word, Excel and Project. Minitab and ORACLE or SAP Enterprise systems

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BioTech FYI Center