-Engage with clients to ensure our research aligns with their needs.-Oversee logistics of importing and exporting cannabis materials and ensure compliance with regulations and coordinate with suppliers and authorities.-Actively contribute to product development and collaborate with teams to innovate and improve formulations, meeting the diverse needs of patients.-Implementing change controls and manage modifications to SOP to ensure integrity in outcomes.Conduct process and software validation studies to verify effectiveness of methodologies in accordance with standards and regulations.-implementation of inventory software and compliance with regulatory requirements for tracking cannabis materials.-Function within the quality assurance group and uphold standards in the manufacture of premium medicinal cannabis products through rigorous testing and analysis.-Manage on-site quality control lab and ensure safe and compliant research operations in the laboratory.-Trend Certificates of Analysis to assess product quality-Ensure compliance with labeling requirements, select product packaging to promote safe use by consumers.-Maintain PMP compliance and implement procedures and support audits to meet regulatory standards.- Collaborate with state-approved labs to ensure products meet regulatory specifications through analytical testing.-Investigate adverse event reports and identify root causes to implement corrective actions.-Support quality standards for cultivation and ensuring organic certification.-Engaging in all production stages, I drive innovation and optimization for enhanced product quality and patient outcomes.-Prioritizing production efficiency, I minimize costs to deliver high-quality products at an affordable price.

Assisted with various farm activities including building greenhouses, building beds, transplant, cloning, bucking, trimming, harvest, light dep, METRC, etc. Supported production of 100% organic flower. Cultivars through the years at production scale: Biscotti, Mochi, Runtz, Jungle Cake, Do-si-dos, Jealousy, Blueberry Muffin, Pineapple Upside-down Cake, Skywalker OG, SFV OG, GSC, Animal Cookies, Gelato, Wedding Cake, ICC, Mac 1, Sour Diesel, GG4, Jacky White, Sunset Sherbet, Green Crack, Blue Dream, Lemon Kush

- Act as a POC for quality issues and decision making, in conjunction with shift supervisors and leads.- Serve as a technical and quality resource for your shift by learning and cascading knowledge of 1QMS/Veeva System [Unplanned Event (UPE) process, UPE closure], Document Review, Batch Record Review (BRR)- Collaborate and build productive relationships with Frontline QA, fellow Compliance Shift Leads, MCAs, support groups, and counterparts in partner organizations.- Communicate information on UPEs between shifts and sides of the week.- Stewardship of the UPE business process & driving continuous improvement of the process.- Train shift members on UPE decision making, process, and closure, working to ensure adequate quality acumen on shift.

▪ Represents the department on cross-functional project teams. Coordinates with technology, Facilities, Engineering and SHE to optimize equipment performance.▪ Process monitoring and trending across all shifts.▪ Expert in business support systems (SAP, POMS, PI) and facility systems (water, CIP).▪ Collects, interprets, and communicates process metrics; utilize metrics to recommend improvements.▪ Thorough knowledge of biopharm technology, processes and the underlying scientific concepts.demonstrate a full knowledge of both general and specific aspects of multiple manufacturingdepartments and processes▪ Troubleshoots and investigates complex problems, works with others to implement solutions.Exhibit detail oriented documentation skills.▪ Communicates effectively and ability to work in a team environment.▪ Exhibits professional interpersonal skills.

- Serves as an example and advocate of ingrained quality- Champions safety improvements and encourages safe work practices in department- Contributes to a LEAN work environment by acting as a change agent and utilizing OE Tools- Contributes to the improvement of training material and practices- Serves as department representative on cross-functional teams- Demonstrates Roche Leadership Competencies within Department and to the site- Acts as SME to regulatory agencies- Leads troubleshooting efforts to resolve complex process issues

Performs operations in the Buffer Preparation, Chromatography, and Final Formulation areas of Purification.Additional Contributions:- Batch Record Review- Discrepancy Ownership and Management- Change Management, SOP Redlines, & Training Material Audits- Provide training to new hires- Ongoing facility maintenance and cleanliness- Safe Working Practices & Safety Suggestions

Generating and characterizing mutations/wild type of Alanine Racemase (Vitamin B)

Davis Fire Crew Type II Handcrew