Portsmouth, NH30+ days ago
Writing- Quality Records (Deviations, CAPA, Change Control) and Test Methods Projects such as method transfers, new instruments, method qualifications Use of Microsoft Suites (Word, Excel, PowerPoint) Use of Laboratory computer systems Potential previous use of GMP Quality Systems such as: TrackWise, LIMS Works on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required. Works entire assigned shift, including arriving on time Has experience with or currently uses the following software: SoftmaxPro, Empower, SoloVPE Has experience with software validations including but not limited to: writing GMP procedures and validation documents and executing test scripts.