Traditional Medicinals

Job Description Summary: The Automation Engineering Technicians on 3rd Shift (11pm to 7:30am) plays a crucial role in ensuring the smooth and efficient operation of automation equipment within our manufacturing facility. This role involves overseeing, maintaining, and optimizing automated systems, as well as providing leadership and technical support to the team. The Automation Engineering Technician is responsible for upholding safety standards, minimizing downtime, and driving continuous improvement initiatives. Key Responsibilities: Manage the operation of automation equipment to maintain consistent production levels, reduce downtime, and ensure product quality. Maintain equipment, maintenance schedules and repairs to prevent or to promptly address equipment breakdowns. Maintain accurate records of equipment performance, maintenance tasks, and any required repairs. Assist in the installation and setup of new automation systems, ensuring proper calibration and functionality Collaborate with engineering and production teams to identify opportunities for process optimization, cost reduction, and quality enhancement. Safety Compliance: Enforce safety protocols and ensure compliance with industry standards to maintain a safe work environment. Participate in safety teams. Utilize the CMMS, Quality software, ERP and other programs or software to optimize production. Qualifications : 3 - 5 years of applicable experience working in maintenance and automation. High school diploma or equivalent; a technical degree or certification in automation, engineering, or a related field is a plus. Proven experience in the operation and maintenance of automation equipment. Knowledge of PLCs (Programmable Logic Controllers) and basic understanding of automation controls is desirable. Ability to read and interpret technical manuals and schematics Strong problem-solving skills and the ability to troubleshoot technical issues. Strong interpersonal communication and leadership skills, supporting an interactive team culture. Leadership and team management skills. Knowledge of safety regulations and industry standards related to automation. Excellent communication and collaboration skills. Travel : Travel to the corporate office in California may be required in the first few months for training purposes Physical/Mental Requirements: An employee must meet the physical demands described here to perform the essential functions of this job successfully. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. While performing the duties of this job, the employee is regularly required to sit and talk or hear. The employee is occasionally required to stand, walk, reach with hands and arms, and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 30 pounds. Specific vision abilities required by this job include close vision. This position is based in Rocky Mount, VA and is onsite Monday through Friday supporting a three-shift operation. Remote candidates will not be considered for this role. Compensation : $31.50 - $41.86 per hour 15% Shift Differential Compensation is determined based on non-discriminatory, business-related factors, including, but not limited to, training, experience, education, and/or professional certifications, geographic location, and market data. Traditional Medicinals, Inc. and its subsidiaries are proud equal-opportunity employers. We wholeheartedly embrace authenticity, diversity, and people's differences. We acknowledge, celebrate, and support individuality to the great advantage of our consumers, stakeholders, products, and the planet. We are committed to building an inclusive workplace for all our people. We do not discriminate based on race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. PandoLogic.

Job Description SUMMARY The Quality Supervisor supervises Quality staff in their day-to-day responsibilities. Ensures in-process quality functions are executed, and manufacturing operations are in compliance with company policies, procedures, and applicable cGMP requirements. Ensures timely disposition of incoming ingredients, component, blends, and finished goods. This position also ensures lab activities are compliant, accurate and documented. ESSENTIAL FUNCTIONS Supervise day-to-day activities and training of Quality department personnel including quality inspectors and laboratory personnel. Ensure timely and accurate inspection, testing and disposition of QC samples (e.g., components, ingredients, blends, finished products, pre-ship samples, retest materials, R&D materials) Ensure all lab instrumentation/equipment is functioning properly, validated for use, and appropriately scheduled for preventative maintenance and calibration Lead OOS investigations with focus on identifying root causes and taking corrective action where appropriate; document and communicate non-conformances to stakeholders Ensure accuracy and completeness of documentation (e.g., batch records, evaluation forms, deviations, NCMRs, Corrective Actions, including electronic/digital records) Partner with Production, Research & Development, Procurement and Planning, and other departments to understand production or corporate priorities and adjust personnel and department priorities as needed Ensure that processes and methods utilized in the laboratory are compliant and accurate Ensure that department personnel are properly trained and qualified to perform their job Ensure compliance with current company, departmental and regulatory requirements Ongoing assessment of facility operations considering continuous improvement Assists and performs data collection and analysis of QC metrics Generates or revises controlled documents such as SOPs and data forms Lead for special projects as assigned Perform maintenance, data entry, and analysis in various electronic systems utilized by the company Perform Quality Inspector duties as backup when needed Site QMS systems subject matter expert (e.g. Redzone, Master Control, Ignition, etc.) Other duties as assigned SUPERVISORY/BUDGET Direct supervision of Quality department inspectors and lab technicians No direct budgetary oversight REQUIREMENTS Education and Experience: BA or BS in scientific discipline or equivalent education/experience Two years' Quality experience in a regulated industry Four years' hands-on QC or analytical chemistry experience in a regulated industry 2+ year supervisory experience in a comparable setting Project management experience preferred Knowledge/Abilities/Skills: Strong knowledge of cGMP requirements and quality systems within a regulated industry, such as food, dietary supplements, cosmetics, or pharmaceuticals, required. Knowledge of regulatory requirements for dietary supplements (21 CFR Part 111) preferred. Technical proficiency in analytical methodologies Strong knowledge of laboratory protocols and equipment Demonstrated ability to manage and develop staff Able to collaborate, influence and work effectively across multiple departments Ability to read and interpret regulatory documents Able to independently solve problems and make decisions based on company and/or quality policy Ability to effectively manage competing priorities with the drive and ability to meet deadlines Excellent organization skills and attention to detail Strong verbal and written communication skills Commitment to and ability to demonstrate TM's Company values: humility, respect, quality, collaboration, innovation and sustainability Pay Range: $34.00 - $41.00 Technical Skills: Intermediate MS Suite WMS/ERP systems preferred Travel Requirements: Occasional travel to California or 3rd party test labs or supplier(s) Work Environment: Works often in the QC laboratory with hazardous chemicals present, requiring competence and familiarity with safe handling and storage of acids, bases and solvents. Works often in production area(s)warehouse, must follow GMP requirements and safety precautions for each area. Traditional Medicinals, Inc. and its subsidiaries are proud equal-opportunity employers. We wholeheartedly embrace authenticity, diversity, and people's differences. We acknowledge, celebrate, and support individuality to the great advantage of our consumers, our stakeholders, our products, and the planet. We are committed to building an inclusive workplace for all our people. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. PandoLogic.

Job Description Summary: The Automation Engineering Technicians on 3rd Shift (11pm to 7:30am) plays a crucial role in ensuring the smooth and efficient operation of automation equipment within our manufacturing facility. This role involves overseeing, maintaining, and optimizing automated systems, as well as providing leadership and technical support to the team. The Automation Engineering Technician is responsible for upholding safety standards, minimizing downtime, and driving continuous improvement initiatives. Key Responsibilities: Manage the operation of automation equipment to maintain consistent production levels, reduce downtime, and ensure product quality. Maintain equipment, maintenance schedules and repairs to prevent or to promptly address equipment breakdowns. Maintain accurate records of equipment performance, maintenance tasks, and any required repairs. Assist in the installation and setup of new automation systems, ensuring proper calibration and functionality Collaborate with engineering and production teams to identify opportunities for process optimization, cost reduction, and quality enhancement. Safety Compliance: Enforce safety protocols and ensure compliance with industry standards to maintain a safe work environment. Participate in safety teams. Utilize the CMMS, Quality software, ERP and other programs or software to optimize production. Qualifications : 3 - 5 years of applicable experience working in maintenance and automation. High school diploma or equivalent; a technical degree or certification in automation, engineering, or a related field is a plus. Proven experience in the operation and maintenance of automation equipment. Knowledge of PLCs (Programmable Logic Controllers) and basic understanding of automation controls is desirable. Ability to read and interpret technical manuals and schematics Strong problem-solving skills and the ability to troubleshoot technical issues. Strong interpersonal communication and leadership skills, supporting an interactive team culture. Leadership and team management skills. Knowledge of safety regulations and industry standards related to automation. Excellent communication and collaboration skills. Travel : Travel to the corporate office in California may be required in the first few months for training purposes Physical/Mental Requirements: An employee must meet the physical demands described here to perform the essential functions of this job successfully. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. While performing the duties of this job, the employee is regularly required to sit and talk or hear. The employee is occasionally required to stand, walk, reach with hands and arms, and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 30 pounds. Specific vision abilities required by this job include close vision. This position is based in Rocky Mount, VA and is onsite Monday through Friday supporting a three-shift operation. Remote candidates will not be considered for this role. Compensation : $31.50 - $41.86 per hour 15% Shift Differential Compensation is determined based on non-discriminatory, business-related factors, including, but not limited to, training, experience, education, and/or professional certifications, geographic location, and market data. Traditional Medicinals, Inc. and its subsidiaries are proud equal-opportunity employers. We wholeheartedly embrace authenticity, diversity, and people's differences. We acknowledge, celebrate, and support individuality to the great advantage of our consumers, stakeholders, products, and the planet. We are committed to building an inclusive workplace for all our people. We do not discriminate based on race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. PandoLogic.

Job Description SUMMARY The Quality Supervisor supervises Quality staff in their day-to-day responsibilities. Ensures in-process quality functions are executed, and manufacturing operations are in compliance with company policies, procedures, and applicable cGMP requirements. Ensures timely disposition of incoming ingredients, component, blends, and finished goods. This position also ensures lab activities are compliant, accurate and documented. ESSENTIAL FUNCTIONS Supervise day-to-day activities and training of Quality department personnel including quality inspectors and laboratory personnel. Ensure timely and accurate inspection, testing and disposition of QC samples (e.g., components, ingredients, blends, finished products, pre-ship samples, retest materials, R&D materials) Ensure all lab instrumentation/equipment is functioning properly, validated for use, and appropriately scheduled for preventative maintenance and calibration Lead OOS investigations with focus on identifying root causes and taking corrective action where appropriate; document and communicate non-conformances to stakeholders Ensure accuracy and completeness of documentation (e.g., batch records, evaluation forms, deviations, NCMRs, Corrective Actions, including electronic/digital records) Partner with Production, Research & Development, Procurement and Planning, and other departments to understand production or corporate priorities and adjust personnel and department priorities as needed Ensure that processes and methods utilized in the laboratory are compliant and accurate Ensure that department personnel are properly trained and qualified to perform their job Ensure compliance with current company, departmental and regulatory requirements Ongoing assessment of facility operations considering continuous improvement Assists and performs data collection and analysis of QC metrics Generates or revises controlled documents such as SOPs and data forms Lead for special projects as assigned Perform maintenance, data entry, and analysis in various electronic systems utilized by the company Perform Quality Inspector duties as backup when needed Site QMS systems subject matter expert (e.g. Redzone, Master Control, Ignition, etc.) Other duties as assigned SUPERVISORY/BUDGET Direct supervision of Quality department inspectors and lab technicians No direct budgetary oversight REQUIREMENTS Education and Experience: BA or BS in scientific discipline or equivalent education/experience Two years' Quality experience in a regulated industry Four years' hands-on QC or analytical chemistry experience in a regulated industry 2+ year supervisory experience in a comparable setting Project management experience preferred Knowledge/Abilities/Skills: Strong knowledge of cGMP requirements and quality systems within a regulated industry, such as food, dietary supplements, cosmetics, or pharmaceuticals, required. Knowledge of regulatory requirements for dietary supplements (21 CFR Part 111) preferred. Technical proficiency in analytical methodologies Strong knowledge of laboratory protocols and equipment Demonstrated ability to manage and develop staff Able to collaborate, influence and work effectively across multiple departments Ability to read and interpret regulatory documents Able to independently solve problems and make decisions based on company and/or quality policy Ability to effectively manage competing priorities with the drive and ability to meet deadlines Excellent organization skills and attention to detail Strong verbal and written communication skills Commitment to and ability to demonstrate TM's Company values: humility, respect, quality, collaboration, innovation and sustainability Pay Range: $34.00 - $41.00 Technical Skills: Intermediate MS Suite WMS/ERP systems preferred Travel Requirements: Occasional travel to California or 3rd party test labs or supplier(s) Work Environment: Works often in the QC laboratory with hazardous chemicals present, requiring competence and familiarity with safe handling and storage of acids, bases and solvents. Works often in production area(s)warehouse, must follow GMP requirements and safety precautions for each area. Traditional Medicinals, Inc. and its subsidiaries are proud equal-opportunity employers. We wholeheartedly embrace authenticity, diversity, and people's differences. We acknowledge, celebrate, and support individuality to the great advantage of our consumers, our stakeholders, our products, and the planet. We are committed to building an inclusive workplace for all our people. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. PandoLogic.