BEPC Inc. - Business Excellence Professional Consulting
Clinical Research Associate
BEPC Inc. - Business Excellence Professional Consulting, Tucson, Arizona, United States, 85718
BEPC Inc. - Business Excellence Professional Consulting has an open position for a Clinical Research Associate III in Oro Valley, AZ. W2 Contract 2 years with the possibility of extensions.
Overview
Individual contributor responsible for project providing support for a wide variety PCQT (Product Care and Quality Team) projects. Performs reagent-based or assay-based investigations to address reagent quality, performance or compliance on-market product issues. Scope includes primary stains, advanced staining reagents, special stains, and bulk reagents used for automated H&E, IHC (immunohistochemistry) and ISH (in-situ hybridization) applications. Works collaboratively across functions including Global Operations or Manufacturing, Complaint Investigation and Resolution, Global Customer Support, Lifecycles, Product Development, Quality, Regulatory, and Global organizations. Responsibilities
Designs a wide range of experimental protocols. Executes bench experiments; makes detailed and general observations and analyzes data. Prepares technical reports, summaries and quantitative analyses. Maintains complete and accurate records. Normally receives general directions on routine and new assignments. Identifies and implements improvements to work processes and laboratory environment. Works on complex problems in which analysis of situations or data requires an in-depth evaluation of various factors. Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results. Participates in cross functional technical teams such as a failure investigation or core team. Works well in a team environment by being a productive project team member, suggesting creative solutions to problems and providing input to project planning. Establishes interfaces across other organizational groups. Troubleshoots problems and institutes corrective action. Prepares and presents experimental procedures and results in group and project teams. Monitors work to ensure quality, and continuously promote Quality First Time. Qualifications
Formal Training/Education Bachelor's Degree Experience 4 years relevant job experience. Employment type
Contract Job function
Research and Science Industries
Biotechnology Research and Pharmaceutical Manufacturing
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Individual contributor responsible for project providing support for a wide variety PCQT (Product Care and Quality Team) projects. Performs reagent-based or assay-based investigations to address reagent quality, performance or compliance on-market product issues. Scope includes primary stains, advanced staining reagents, special stains, and bulk reagents used for automated H&E, IHC (immunohistochemistry) and ISH (in-situ hybridization) applications. Works collaboratively across functions including Global Operations or Manufacturing, Complaint Investigation and Resolution, Global Customer Support, Lifecycles, Product Development, Quality, Regulatory, and Global organizations. Responsibilities
Designs a wide range of experimental protocols. Executes bench experiments; makes detailed and general observations and analyzes data. Prepares technical reports, summaries and quantitative analyses. Maintains complete and accurate records. Normally receives general directions on routine and new assignments. Identifies and implements improvements to work processes and laboratory environment. Works on complex problems in which analysis of situations or data requires an in-depth evaluation of various factors. Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results. Participates in cross functional technical teams such as a failure investigation or core team. Works well in a team environment by being a productive project team member, suggesting creative solutions to problems and providing input to project planning. Establishes interfaces across other organizational groups. Troubleshoots problems and institutes corrective action. Prepares and presents experimental procedures and results in group and project teams. Monitors work to ensure quality, and continuously promote Quality First Time. Qualifications
Formal Training/Education Bachelor's Degree Experience 4 years relevant job experience. Employment type
Contract Job function
Research and Science Industries
Biotechnology Research and Pharmaceutical Manufacturing
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