Lead Quality Assurance Technician - Kennesaw, GA NATURE & SCOPE The primary function of this role is to assist with the management and oversight of the good manufacturing practices and the quality of raw materials and finished goods used by and/or manufactured at Deerland Probiotics and Enzymes. This role is to be a “hands on” lead that oversees and performs quality assurance functions and assists in compliance with internal and external regulations, protocols, and policies. MAJOR ACCOUNTABILITIES Ensure cGMP standards are properly implemented and carried out throughout the organization. Ensure that the facility and products meet all local and federal food/supplement safety regulations Act as a facilitator/coach in areas such as Quality techniques, Good Manufacturing Practices, and product quality/safety Sample and analyze raw materials, in process goods, and finished products to assure compliance to specifications Perform line clearance using, but not limited to, ATP technologies Maintain inventory of sampling / QA testing supplies. Assist or conduct audits with the Quality team including, but not limited to, Good Manufacturing Practices and Food Safety Oversee quality auxiliary programs such as but not limited to air differentials, glass and brittle plastic, EMP, quarantine audits. Record and evaluate test data, alerting Quality Manager to any deviations from specifications Assist in data collection and analysis for ongoing quality improvements Partner with plant operations, maintenance, compliance, quality and engineering to ensure that good manufacturing practices, sanitation and pest control programs, procedures and systems are effectively monitored per policy requirements Partner with plant operations, maintenance, quality and engineering to develop, write, review and train on Standard Operating Procedures and Policies, Work Instructions, and Forms Partner with operations team to build a strong food safety culture, to ensure pre-requisite programs are effective for producing a safe food/supplement products and to facilitate the successful execution of customer, regulatory, and certification audits Assist in performing quality document activities including, but not limited, issuing master manufacturing records, review and approving batch records and work insturctions, ensuring logs and records are appropriately completed and maintained, reviewing and approving shipping documention, and filing and maintaining all records as required Ensure new / revised SOPs and continuous improvement efforts are communicated and implemented. Other duties as assigned
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Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED