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ICONMA, LLC Quality Control Research Associate I in United States

Quality Control Research Associate I Location: El Segundo (onsite) Duration: 12 13 months Description: Support activities related to documentation review and QC data package generation for product release. Reviews data and results of testing completed by QC to ensure compliance to appropriate specifications and protocols. Monitoring product and testing schedules and provide notification support to QC. Apply knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Practices (GLPs) on a daily basis. Must have working knowledge of Microsoft Office software and Adobe. Participates in group meetings. Interact with cross-functional group. Ideally, prefer someone with 1-2 years experience in a GMP setting. Top 3 skill set: Attention to details, organized and can handle multiple projects/tasks at a the same time, knowledge of lab testing process Top Nice to have skill set: Experience with Adobe Acrobat Pro, hands on experience in a testing lab This is a great opportunity for CW to work directly with the process of releasing product to treat cancer patients 30% document reviewing 40% putting together QC data packages for review by compliance groups 20% other office related tasks 10% meeting As an equal opportunity employer, ICONMA prides itself on creating an employment environment that supports and encourages the abilities of all persons regardless of race, color, gender, age, sexual orientation, citizenship, or disability.

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