Logan Johnson Email & Phone Number

Columbus, Oh, Us

Columbus, Oh, Us

United States

Columbus, Ohio, United States

Responsible for developing, documenting, and refining product processes, and constructed their foodsafety and food defense systems.Assembled the company’s HACCP plan, and built the company’s food defense, sanitation, andworkplace safety systems.Constructed QC protocols to measure and improve product quality.Assembled the information and documents needed for their product Challenge Study.Built employee food safety, allergen, sanitation, and workplace safety training program. Trained various members of production, as well as leads and management.

United States

Supervised 3-8 QA techs. Provided assistance and guidance when food safety, sanitation, and quality control issues arose. Daily tasks included:Training Production employees, as well as my own members on various food safety, food defense, safety, and sanitation topics.Reviewing shift paperwork, filling for technicians for various tasks throughout shiftsConducting shelf life studies, researching and completing Food Safety projectsConducting internal audits of the quality system and work environment. Assisted with Federal and 3rd party system/facility inspections.Assigning and completing Corrective Actions and NUOCA’sReviewing payroll, timecards, and inventory. Placed supply orders, as well as creating and adjusting department schedules.Wrote SOPs, SSOPs, and training documents, and product specification sheets.

Johnstown, Oh

Oversaw site compliance with Company standards, as well as Local, State, and Federalregulation. Responsibilities included:Conducting internal audits, and assigning/performing any Corrective Actions.Assisting QA/QC with microbiological and Quality tasks.Oversaw the farm’s ODA and OEPA site and environmental permits, and write/updaterelevant SOPs and policies.Training employees, reviewing weekly paperwork.Working as one of the points of contact for ODA/OEPA personnel during siteinspections

Zanesville, Oh

Responsible for maintaining Klarity QMS, Which covered 21 CFR 820 & ISO:13485. Responsibilitieswere:Opening, investigating and closing out customer cases as well as CAPA’s, and NCR’s.Product design and review, ensuring validation and verification of various products.Conducting internal audits, and leading the company through FDA audits.Maintaining device records of manufactured products.Organizing and updating device history files.Building, then maintaining the company’s GUDID submissions. Includes designing andmaintaining their product and package labeling system.Reviewed product packaging for any improvements.Inspected received product shipments for Quality issues