Laboratory Technician

• Conduct Quality Control Testing: • Perform chemical and physical laboratory tests to determine if materials meet quality specifications. • Evaluate raw materials, in-process goods, and finished products for compliance with company and state specifications. • Perform QC sampling of materials and products. • Conduct routine quantitative HPLC analysis on a variety of sample matrices. This includes sample preparation, system calibration, maintenance, and troubleshooting. • Perform microbial detection by qPCR, including sample preparation using aseptic techniques. • Conduct Hop Latent Viroid (HLVd) detection by RT-PCR Lamp and qPCR technology, including plant root sample collection and preparation using aseptic techniques. • Perform water microbiological analysis, including water collection, preparation, and analysis utilizing Petrifilm microbial testing. • Perform QC flower inspection utilizing handheld digital microscope, moisture content analyzer, and water activity meter. • Environmental Monitoring: • Conduct semi-quantitative microbial assessments via surface and settle plate sampling. • Identify and subculture microorganisms; arrange for speciation of unidentified strains. • Perform ATP swab testing for surface cleanliness. • Monitor and record facility environmental conditions. • Daily Verifications: • Confirm and verify that all cultivation, processing, packaging, and manufacturing SOPs are being followed; responsibilities are being conducted; documented and up to date. • Perform daily in-process verifications. • Communicate issues, report findings, and follow-up on corrective actions. • Laboratory Operations and Maintenance: • Prepare and/or standardize solutions for testing. • Maintain stock of laboratory supplies and chemicals. • Keep accurate logbook records of testing analysis, inspection of raw materials and products and material retains, as well as other records as required. • Perform routine instrument calibration, maintenance and minor repairs. • Clean glassware and refill/replace items/solutions as needed. • Store supplies and equipment and dispose of waste per state regulations. • Quality Assurance Support: • Assist in approving and releasing materials from inventory for use in facility. • Assist in the investigation of product complaints. • Manage lab documentation and support manufacturing efforts as needed. • Safety and Compliance: • Comply with established safety standards for proper use, safe handling, and disposal of harmful chemicals, substances, and hazardous wastes. • Adhere to cGMP pharmaceutical manufacturing practices. • Regular attendance is required. • Other Duties: • Perform other duties as required.

• Must be at least 21 years of age. • Must not have been convicted of any felony offenses pursuant to state statutes. • QA/QC Experience a plus. • Knowledge of cGMP manufacturing preferred. • Minimum 1-2 years' experience in HPLC Analysis preferred. • Minimum 1-2 years’ experience conducting microbial analysis using pPCR and/or plating preferred • Bachelor’s degree in Biology, Chemistry, or a related field preferred. • Effective verbal and written communication skills. • Proficiency in MS Office suite. • Analytical with the ability to collect and interpret data. • Strong organizational skills with the ability to multitask and prioritize competing demands. • Ability to comply with established safety standards for the proper use, safe handling, and disposal of harmful chemicals, substances, and hazardous wastes. • Experience effectively using computer systems, software, and hardware common to laboratories and recordkeeping procedures. • Must be able to work in a challenging, fast-paced environment while maintaining strong attention to detail. • The performance of this position normally requires exposure to manufacturing areas where the use of personal protective equipment, such as safety glasses, and hygienic precautions, such as hairnets, are required.