Edgar Walton Jr Email and Phone Number

- Practice safe working techniques and re-enforce company EHS policies and guidelines and procedures.- Provided daily guidance and direction in EHS programs at the associate/supervisor level to ensure a common and effective approach.- Design and present training programs for new hires and current team members, addressing relevant health, safety and /or environmental issues.- Maintain facility specific EHS procedures for safe work practices and equipment operation.- Perform storm water monitoring and sampling for the facility.- Maintain Hazardous, Non Hazardous, and Universal waste areas, and perform regular waste disposal practices according to TCEQ and federal regulations.- Assist managers/supervisors with accident response, including during off hours and on weekends.- Document daily safety observations to ensure all hazard risks are minimized to prevent accidents from happening.- Perform PPE assessments and provide the proper PPE to each specific department.

Served as lead technician charged with leading team in the production and synthesis of both TCP and CSD. Led production of bone cement materials used in a variety of orthopedic and craniofacial applications. Interfaced directly with Research and Development team to gather project data, establish testing/production procedures, execute production reviews to ensure quality and on time delivery of products. Conducted product inspections and quality control processes to approve product formulation. Conducted weekly safety audits of the entire facility, including the Research and Development and QC Labs; devised and performed strategies to properly handle and remove hazardous waste material. Performed periodic production equipment maintenance and preventive maintenance tasks and documented maintenance activities. Established and maintained vendor relations.

- Coordinated work order Bill of Materials for the filling department. Maintained inventory supplies by performing routine cycle counts and ordering replacement supplies. Operated manufacturing equipment (filling , labeling and Sartocheck Filter Integrity tester) efficiently and safely, while maintaining a high standard of quality. Maintained lot specificity and batch record traceability of components and associated material. Maintained records used to establish Device History records. Ensured that all rejected material was handled in accordance with FDA and DEA guidelines. Disposed Hazardous waste material, and / or Proposition 65 listed material in accordance with Environmental Health and Safety guidelines. Trained temporary employees to work in a GMP / ISO 9001 facility.- Excelled in writing and revising SOPs, departmental procedures and spread sheets.- Experienced in antibody and antigen diluent and reagent manufacturing. This includes but is not limited to the following: staging product builds by weighing measuring and securing all material used per work order.- Lead consultant for the validation of two automated liquid reagent filling rooms.- First representative for the "KAIZEN" streamlining process.- Initiated and executed IQ/OQ validation protocols for new and existing equipment.- Participated in the ISO 9000/9001 certification for the filling department.

- Secure & weigh all raw materials for product formulation.- Manufacture multiple large volume liquid solutions in accordance with SOPs and documented formulas.- Breakdown, clean, set up, and operate fill room equipment in a class 10,000 environment.- Clean and sanitize sterile areas.- Maintain compliance with cGMP and SOPs.