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ASI is looking for a QA validation engineer who is looking for an exciting opportunity with a large company.   Job Description: Review manually executed SAP test cases against captured objective evidence in HP Quality Center, to validate the results. Must be willing to work long hours, or over the weekends, when requested to meet aggressive deadlines.

Innovation and quality lead the way for this progressive, rapidly growing manufacturer.  Join their dynamic team and receive a competitive salary and great benefits.   $100,000 TO $115,000 BASE SALARY + PERFORMANCE BASED BONUS 

New Breed Logistics is an innovative third-party logistics service provider (3PL) that helps companies design and operate efficient supply chains. We manage millions of square feet of warehouse space across more than 50 distribution centers in the U.S.

Business Unit:  L-3 Global Security and Engineering Solutions Job Type:  Full-Time Job Description:   If you thrive on challenge and are motivated, creative, and can hit the ground running, we want you on our team! Headquartered in Billerica, Massachusetts, Engility Corporation is a systems acquisition solutions and services provider. Engility's proven engineering professionals, management team, grounded in disciplined engineering process, have more than 25 years experience.

This temp assignemt requires the candidate to have recent experience using micrometers, calipers and other instruments use to measure parts. The candidate must also be able to read blue prints. Working hours: 7am until 3.

Under general supervision, utilizing judgment and sound decision-making skills, assists in the implementation of the Quality Improvement Program, performing independent data collection, reporting, and analysis. - Assists in the monitoring of the organization's compliance with standards of the Office of Behavioral Health Licensure (OBHL) and any contracted source or regulatory or accreditation entity - Performs audits of client records regarding outcomes studies, benchmarking of quality indicators, and requesting/maintaining corrective action plans - Assists with grievance investigation follow-up, resolution, database maintenance, and report compilation - Compiles minutes and maintains records for the Quality Improvement Team and Health and Safety Team - Is an active member of the Health and Safety Team and functions as the Safety Coordinator - Assists in the development/implementation of systems and/or training to address deficiencies identified through a systematic process - Serves as a resource to staff regarding federal, state, and local regulations - Participates in assuring a visible presence of the QI Department at staff and client locations  

Position Summary: This position is responsible for scheduling and overseeing daily activities for the quality assurance associates supporting parenteral manufacturing and packaging/labeling operations.  Additionally, the position assists in performing technical and administrative review of batch and analytical data for accuracy and compliance to procedures for raw material, in-process, and product release as it relates to parenteral manufacturing.    Primary Responsibilities: (will include other duties as needed) Coordinate activities related to implementation of Quality Assurance programs, processes and facilities by ensuring regulatory compliance in the manufacture of products from beginning to end Supervise activities of direct reports in the conduct of duties Review and approve SOPs for quality impact and compliance with regulations Perform technical and administrative review of batch and analytical data generated by manufacturing and GMP and GLP test laboratories relating to raw material, in-process and product release Participate in investigations and corrective action identification and implementation process for OOL and Exceptions Support GMP training program for company employees Participate in internal and external audits as needed Track and trend quality metrics including CAPA and PPQE

Director of QA Klosterman Baking Company is looking for a Director of QA to oversee multiple locations. Must have a degree, knowledge of quality systems pre-requisite programs such SPC, process improvement skills and food safety; external audit experience, and customer interaction. Operations and management experience a plus.

We are seeking an experienced and detail oriented Scientist to join our Quality Assurance team. At Promega, QA Scientists are part of new product development, specification development, change management and review/release of products, literature content and control.  This position has extensive involvement across the organization with areas such as R&D, Manufacturing and Marketing regarding product or process improvements, product development and commercialization, and Custom Order fulfillment.