Ensure accurate, reproducible, and timely QC testing in support of manufacturing; support development, validation and stability studies on an as-needed basis; participate in methods improvements within the laboratory. They will identify and report OOT and OOS results as testing is in progress; assist in troubleshooting equipment and method failures; perform testing on in-process product, final product, and raw materials for routine testing, validation testing, and stability testing; communicate results through appropriate documentation and batch records, statistical analysis and trending; support off shift work as required. They will also serve as a resource for staff and assist with training of chemists; lead projects to improve efficiency; assist with writing variance and corrective actions as they relate to the laboratory.
Requirements: BS in Chemistry or related life science with 5-8 years experience in lab applications. FDA regulated industry experience; hands on experience with HPLC; in-depth knowledge of current technology and methodology; high attention to detail.
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