A services company in Lawrence Kansas is currently seeking a new GMP Documentation Review Specialist for a great opportunity with their team. In this role, the GMP Documentation Review Specialist will be responsible for reviewing, interpreting, and analyzing documents and data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP). Will performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.Responsibilities: The GMP Documentation Review Specialist will:Review draft protocols and procedures for accuracy and completion against SOP's, Specifications and requirements trace matrices.Perform Documentation QC Checks on draft protocols and reports.Manage the routing to approve and incorporation of comments.Support Commissioning, Qualification and Validation resources with managing discrepancies and GDP.Review executed protocols for completeness, focusing on Good Documentation Practices and assurance that data is attributable, legible, contemporaneous, original, and accurate.Work with Commissioning, Qualification and Validation resources to correct issues.Manage the review and approval of post executed protocols and test plans.Draft Standard Operating Procedures/Control Forms.Support QA management in the Quality Management System, including.Qualifications:Bachelor's degree in a science-related field or relevant work history in a related positionPrior GXP experience required, preferably cGMP.Ability to multi-task in a fast-paced environmentSelf-starter able to work independently.Excellent verbal and written communication and listening skills required.Experience and proficiency using Microsoft Office ProductsBasic math skillsOutgoing attitude and desire to achieve results.Orientation towards teamwork and a collaborative work environment.