SRG is a global staffing and consulting firm and we are looking for a Contract QC Lead-Data Reviewer for a 12 month plus contract in Morrisville, NC!
The Contract QC Lead Associate, Data Reviewer position is a position that supports a broad range of analytical disciplines within the Quality Control laboratory. The individual performs data review for testing of high throughput, right-first-time laboratory work to meet production schedules and project milestones and will work with minimal supervision. They are expected to follow procedures and have familiarity and proficiency with a wide variety of analytical methods and supporting data management processes. The individual effectively and efficiently manages complex or difficult tasks. Analytical disciplines requiring data review common to the laboratory include, but are not limited to: Chromatography, HPLC, Concentration determination, pH, Total Organic Carbon, Gel based protein separation, IEF, Plate Based Assay, and conductivity.
Other duties and responsibilities include:
Responsible for data review for a broad range of laboratory support functions and procedures as assigned, demonstrating expertise in technical skills, disciplines, and procedures within assigned discipline area(s)
Support the data review for CAPA's, audit actions, deviations, lab investigations, method revisions, and other related Quality System activities. Embrace lean lab and six sigma principles and applies them to laboratory processes.
Reviews technical data and provides expert review and input to new methods and revisions.
Creates data reviews, summary reports, and provides expert interpretation of data. Notifies management and initiates events (such as deviations) in the quality systems. Prioritizes and organizes work to deliver assignment according to established schedules and deadlines. May coordinate logistics associated with laboratory testing or supporting documentation with others in group. May provide technical services (such as preparing reports and initiating deviations) from preexisting templates. Capable of meeting schedule RFT, high quality effort, taking initiative to communicate, coordinate, and adjust work efforts to achieve these objectives. Trainer within areas of proficiency. Assists with deviations, lab investigations, procedure changes, method transfer planning. May have some assigned project responsibilities, such as department representation, document development or review, troubleshooting, and protocol execution. Contributes to achievement of team goals and sense of teamwork within unit and across department. Identifies and solves problems while informing and consulting with area management. Conveys holistic view of data in context of validity, reliability, and impact relative to the batch at hand and other related batches and processes.
Proactively identifies and implements improvements with minimal oversight. Manages multiple assignments of increasing complexity and responsibility. Generate reports and recommendations based on statistical data, can identify statistically significant and impactful events. Performs or leads laboratory investigations, identifies deviations and implements corrective actions. Applies process improvement methodologies that contribute to solutions of technical issues. Can communicate in a manner that fosters cooperation and creates a safe environment for those involved.
This position supports the manufacturing, revenue, and profit plans as they relate to the on-time and error free analysis of product and equipment related samples in the Quality Control Laboratory.
Minimum Education Requirements
BS/BA in science, preferably in chemistry, biochemistry, pharmaceutical sciences, or related technical field.
8+ years related laboratory experience (4 years required with relevant MS degree)Specific Skills and Competencies
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