Luis Adorno

Managed all aspects of laboratory titration using test method, environmental testing, ensuring compliance with regulatory standards and company protocols.

• Scheduled and coordinated environmental companies for waste disposal, optimizing efficiency and minimizing downtime.
• Conducted pH testing of wastewater and stormwater to assess environmental impact and ensure regulatory compliance.
• Oversaw Quality Control (QC) procedures, maintaining high standards of product quality and safety.
• Managed truck loading operations, focusing on QC-related aspects to streamline shipping processes and minimize errors.
• Addressed production quality issues through comprehensive in-process QC procedures, ensuring consistent product quality.
• Conducted incident investigations and prepared detailed reports to identify root causes and implement corrective actions.
• Facilitated bi-weekly Environmental Health and Safety (EHS) safety training sessions, promoting a culture of safety among employees.
• Conducted safety audits and ensured compliance with GHS labeling regulations and Personal Protective Equipment (PPE) utilization.
• Managed contractor safety protocols and supervised contractor employees to ensure adherence to Thatcher Chemicals' policies and OSHA regulations.
• Maintained inventory records in the M3 system, optimizing inventory levels and minimizing stockouts.
• Communicated with Sales regarding order delays, customer complaints, and production/quality issues to ensure customer satisfaction.
• Ensured compliance with financial procedures, including credit card purchases and purchase orders.
• Investigated incidents, accidents, and near misses, submitting reports to the EHS department and participating in incident reviews.
• Enforced proper housekeeping standards throughout the facility and ensured compliance with state, local, and federal regulations.
• Managed annual SOP training, Respirator Fit Testing, and SCBA compliance to maintain a safe working environment.Developed and implemented production schedules using the ERP system, M3, to optimize resource utilization and meet production targets.
• Managed the production team, providing leadership and guidance to ensure efficient operation of manufacturing processes.
• Ensured the production team had access to all necessary raw materials, equipment, and tools to facilitate smooth process flow, especially during shift transitions.
• Conducted titration analyses following laboratory test methods to monitor process parameters and maintain product quality.
• Implemented cost reduction initiatives, process optimization strategies, and profitability improvement measures to enhance operational efficiency and reduce waste.
• Focused on leadership and team development through training programs and performance improvement planning.
• Collaborated with marketing and partnership development teams to identify opportunities for business growth and expansion.
• Implemented measurable metrics to track progress in cost reduction, profitability improvement, process optimization, leadership development, and marketing initiatives.

• Supervised sampling of in-process and raw materials to ensure adherence to company procedures and standards.
• Managed the retain program and conducted quality control inspections to assure compliance with established standards.
• Oversaw environmental monitoring and water system oversight to maintain facility cleanliness and safety.
• Conducted cleaning verifications and approved executed PR specs and inspections on labels.
• Coordinated annual inspections of retains and managed QA retain storage and updates.
• Led on-the-job training for QA inspectors and reviewed and approved in-house release testing.
• Prepared and shipped samples to contract laboratories and performed equipment cleaning verification and validation protocols.
• Conducted protocols for cleaning validations and inspected and tested packaging components for quality assurance.
• Coordinated installation, operational qualification, and performance qualification of new equipment and manufacturing processes.
• Served as the lead QA representative on project teams for pharmaceutical formulation, development, and manufacturing.
• Ensured compliance with CAPA within the Pharmaceutical Quality System and conducted timely review, feedback, and approval of master batch records, reports, qualifications, and test results. Utilized critical thinking and decision-making skills to address quality control issues and implement corrective actions.
• Conducted testing processes and audits to maintain compliance with industry regulations and quality standards.

• Supported adherence to SOPs, GMP, and FDA regulations by assisting in the review and approval of batch records and qualification protocols.
• Sourced and purchased equipment and supplies to support manufacturing operations, ensuring timely availability and compliance with quality standards.
• Assisted in the creation and execution of process and cleaning validation activities to ensure product quality and regulatory compliance.
• Facilitated training sessions for manufacturing personnel to ensure competency and adherence to procedures.
• Created and distributed production schedules, adjusting as necessary to meet production demands and deadlines.
• Assisted in the creation of technical risk assessments to identify and mitigate potential production issues.
• Maintained a comprehensive training program to ensure compliance with regulatory requirements and industry best practices.
• Prepared production equipment and supplies before executing job orders, ensuring readiness and efficiency.
• Operated equipment safely and effectively during production processing, following SOPs and safety protocols.
• Conducted regular inspections of equipment to identify any malfunctions or maintenance needs, facilitating prompt repairs and replacements.
• Acted as a member of the Safety Committee, contributing to the development and implementation of safety initiatives.
• Interviewed new candidates for manufacturing roles, evaluating qualifications and fit for the team.