QC Analyst, second shift

Agilent Technologies • Frederick, MD

2d • $27 - $42

About The Position

Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek -- so they can do what they do best: improve the world around us. Information about Agilent is available at www.agilent.com . Shift schedule: Monday to Friday Shift hours: 1:30 pm to 10:00 pm or 2:30 pm to 11:00 pm, employees choice Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors. Exercises judgment within defined procedures and practices to determine appropriate action. Conducts routine/non-routine analysis and review to support in-process, release, stability and raw materials according to Standard Operating Procedures (SOP) and Analytical Methods in accordance with current Good Manufacturing Practices (cGMPs) and regulatory requirements. Completes projects with supervision. Has a clear understanding of Good Laboratory Practices (GLPs), cGMPS, and other regulatory requirements. Actively engages in continuous improvement of processes and procedures. Proven ability to exercise judgment and appropriately escalates issues to QC management. Has a clear understanding of Good Laboratory Practices (GLPs), cGMPS, and other regulatory requirements. Actively engages in continuous improvement of processes and procedures. Proven ability to exercise judgment and appropriately escalates issues to QC management. Works cross-functionally to complete projects and testing.

Requirements

• Bachelors, Master's Degree or University Degree in the sciences preferred.
• 0 to 2+ years of lab, pharma or biologics experience.
• Has a clear understanding of Good Laboratory Practices (GLPs), cGMPS, and other regulatory requirements.

Responsibilities

• Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors.
• Exercises judgment within defined procedures and practices to determine appropriate action.
• Conducts routine/non-routine analysis and review to support in-process, release, stability and raw materials according to Standard Operating Procedures (SOP) and Analytical Methods in accordance with current Good Manufacturing Practices (cGMPs) and regulatory requirements.
• Completes projects with supervision.
• Actively engages in continuous improvement of processes and procedures.
• Proven ability to exercise judgment and appropriately escalates issues to QC management.
• Works cross-functionally to complete projects and testing.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level