Job Overview Primary Responsibilities
Method Development (MD)
Act on the behalf of the method development Critical Reagent Inventory (CRI) owners to generate sub-aliquots in e-workbook, create labels in nautilus and take care of all labeling requirements Creates CRIs on behalf of method developers for new clients during method development
Establish appropriate low inventory flag thresholds for all reagents through interaction with the method developers and communicate appropriate reagent thresholds downstream to LSPM roles Deliver accurate and complete CRIs to method developers prior to the DEV-VAL hand-off process Maintain MD freezer inventory spaces
Enter orders into the reagent ordering share point site (or similar ordering software system) on behalf of method developers Method Validation (MV) Review client CRIs for daily decrementing and report back non-compliance to MV supervisor Act on the behalf of the validators to generate sub-aliquots in e-workbook, create labels in nautilus and take care of all labeling requirements Check through CRI prior to end of validation for completeness and accuracy and confirm compliance with MV supervisor EducationQualifications BSBA degree in science plus at least 1-2 years of previous laboratory experience.
Relevant experience may be substituted for education.
Experience with routine MS Office suite applications (e.g., Word, Excel, Power Point).Effective communication (verbal and written), presentation and interpersonal skills.
Experience Basic knowledge of computers and software programs.
If possible, familiarity with the use of standard laboratory equipment.
If possible, experience with use and trouble shooting of analytical equipment is desired.
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