QC Chemist

Job Description Quality Control Chemist - Kennesaw, GAThis is a full-time, non-exempt position.NATURE & SCOPEQC Chemist will perform, under the direct supervision of the Senior Chemist, inspection and analysis on raw materials, in-process samples, and finished goods to ensure compliance with cGMP/GLP/ISO standard operating procedures. The scope of responsibility for this position crosses multiple departments within Deerland Probiotics and Enzymes (e.g. Quality Assurance, Production, Sales, etc.); therefore, the incumbent needs to collaborate with various departments and institutions. A successful candidate will be expected to maintain accurate and legible laboratory logbooks and testing documentation in accordance with SOP's.MAJOR ACCOUNTABILITIESThe responsibilities of a QC Chemist include, but are not limited to the following:Perform laboratory tests in a manner such that results are accurate, precise, and reproducibleInspect and analyze raw materials, in-process samples, and finished goods in accordance with cGMP/GLP standard operating proceduresIdentify imperfections of samples with mechanical/electronic equipment and chemical analysisTest chemical and physical samplesDocument data, report results, perform equipment verification and calibration, and laboratory cleaning in accordance with Deerland Enzymes' SOP'sPerform a variety of QC assays with established procedures and SOP'sPreparation of wet and dry samples for laboratory analysisMaintain familiarity with current scientific literature and technologiesCarry out routine tasks and follow strict methodologies to carry out analysesIdentify opportunities for method or SOP improvementEnsure a well-stocked and resourced laboratoryLocal travel (between sites): Occasional (EducationMinimum - Bachelor of Science in Biochemistry, Biology, Chemistry, or equivalentExperienceRequiredProficient in MS Word, Excel, and Power PointBasic mathematical and statistical skillsBasic laboratory skills (e.g. pipetting, weighing, dilutions, etc.)Experience with any of the following: standard assay procedures, IR, HPLC, PCR, Real-Time PCR,Preferred0-3 years of previous laboratory experienceQuality Control and knowledge of cGMP / ISO 17025Specific skillsStrong attention to detail in order to produce accurate, precise, and reproducible dataStrong analytical, organizational, and time management skillsTask oriented and results drivenStrong work ethic and prioritizational skillsWork collaboratively with various departments to compile, analyze, and interpret dataManual dexterityAbility to follow written protocolsAbility to work in a fast paced environmentExcellent written and oral communication skils - ability to make presentations and/or give presentationsMust be able to lift 25lbsMust possess a valid US Driver's LicenseExcited about this role but don't meet every requirement listed? Studies show that often applicants will self-select out if they don't check every box. We encourage you to apply anyway. You may be just the right candidate for this role or another one of our openings. ADM requires the successful completion of a pre-employment drug screen and a background check. "AJCIND"REF:90470BR