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Company | BRILTALENTA |
Address | El Segundo, CA, United States |
Employment type | FULL_TIME |
Salary | |
Category | Staffing and Recruiting |
Expires | 2023-11-20 |
Posted at | 11 months ago |
Below Are The Details
Our client, a leading pharmaceutical company, has a requirement for a QC Research Associate in El Segundo, CA.
Title: Quality Control Research Associate
Job id: GILDJP00013044
Location: El Segundo, CA
Duration: long term contract
Company: leading pharmaceutical company
Responsibilities
Excellent employment opportunity for a Quality Control Research Associate in the Segundo, CA area. (onsite) 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.
Experience
Ideally, prefer someone with 1-2 years of experience in a GMP setting. Top 3 skill set: Attention to details, organized and can handle multiple projects/tasks at the same time, knowledge of laboratory testing process Top Nice to have skills: experience with Adobe Acrobat Pro, hands on experience in a testing laboratory 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 Shift schedule: 4-10, Sunday - Wednesday or Wednesday Saturday, although to start off with (due to training needs), the schedule will start as Monday Friday
Our client, a leading pharmaceutical company, has a requirement for a QC Research Associate in El Segundo, CA.
Title: Quality Control Research Associate
Job id: GILDJP00013044
Location: El Segundo, CA
Duration: long term contract
Company: leading pharmaceutical company
Responsibilities
Excellent employment opportunity for a Quality Control Research Associate in the Segundo, CA area. (onsite) 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.
Experience
Ideally, prefer someone with 1-2 years of experience in a GMP setting. Top 3 skill set: Attention to details, organized and can handle multiple projects/tasks at the same time, knowledge of laboratory testing process Top Nice to have skills: experience with Adobe Acrobat Pro, hands on experience in a testing laboratory 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 Shift schedule: 4-10, Sunday - Wednesday or Wednesday Saturday, although to start off with (due to training needs), the schedule will start as Monday Friday
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