QC Manager will be responsible for maintaining QC standards by overseeing the inspection and testing of materials, components, production, and finished products. The QC Manager will lead and manage daily activities to ensure compliance with applicable regulatory, customers and internal requirements. • Knowledge of quality control methods and techniques • Experience in managing a team and leading quality initiatives • Ability to communicate effectively with executives and team members • Directs and coordinates the activities of the quality control function to ensure achievement of company objectives. • Strong analytical and problem-solving skills • Professional certifications in quality control or quality management are a plus • Evaluates current procedures and practices for accomplishing department objectives; develops and implements improvements as needed. • Initiate ISO Certification process. • Directs and coordinates analysis of products in compliance with ISO, Good Manufacturing Practices (GMP), regulations, and SOPs. • Experience in ISO 9001 and other quality management systems • Develops and implements primary quality control systems consistent with ISO, GMP, and SOPs. • Generates protocols, reports, and SOPs, reviews protocols, SOPs, product specifications, and batch records. • Identifies technical problems and develops solutions. • Oversees completion of appropriate documentation to support testing procedures. • Develops and maintains department budget. • Manages laboratory equipment maintenance schedules; ensures laboratory equipment is maintained in accordance with established schedules, and SOPs. • Hires, trains, supervises, motivates, and develops quality control staff; manages schedules and workflow. • Assigns duties and monitors quality of work; assures staff conforms to organizational policies and procedures and government regulations. • Keeps up to date on overall activities of the team, identifying problem areas and taking corrective actions. QUALIFICATIONS: • M.S. in related field and minimum of three years related experience or B.S. in related field and minimum of five years related experience. • Strong knowledge of Private Label Blending/Formulation/Tolling and Bottling manufacturing processes and equipment validation. • ISO, GMP, SOP, and product/process validation. • Thorough knowledge of ISO, GMP, CFR, and factors impacting compliance. • Knowledge of and ability to utilize statistics in evaluation of data. • Thorough knowledge of ISO regulations. • Experience working with equipment manufacturers • Experience with laboratory environment, equipment, and safety procedures. • Excellent written and oral communication skills • Strong organizational, problem-solving, and analytical skills • Ability to manage priorities and workflow • Versatility, flexibility, and a willingness to work within constantly changing priorities with enthusiasm. Email Resume to: [email protected]
Ki Liquid Engineering
Chemical Manufacturing
Santa Fe Springs, California 418 followers
KI Is a USA chemical blending & formulating, specializing in automotive, janitorial, industrial chemicals, and more.
Über uns
KI Liquid Engineering is a USA chemical blending, formulation, bottling, and logistic company. We are committed to providing an innovative suite of value-added services that will help you develop strong, long-term relationships with your suppliers and provide a single solution for all your needs. We strive to be an integral part of our customers’ success with a global network that has helped us maintain long-term relationships with suppliers and develop products for their needs. We have stayed committed to earning lifetime customer loyalty through innovation, sustainability, and service excellence in everything that we do. At Ki Liquid Engineering, we pride ourselves on our ability to deliver high-quality customer service while maintaining competitive pricing strategies that help businesses save money without compromising on quality standards or speed-to-market requirements. We offer full service from concept through sampling and final packaging, so you don't have to worry about any aspect of the process!
- Website
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http://www.kiliquidengineering.com
External link for Ki Liquid Engineering
- Industrie
- Chemical Manufacturing
- Größe des Unternehmens
- 51-200 Mitarbeiter
- Hauptsitz
- Santa Fe Springs, California
- Typ
- In Privatbesitz
- Spezialitäten
- Private Label, White Label, Product Development, Bottling & Labeling, CoPacking, Logistic Support, Custom Blending, Car Care, Marina Care Products, Pet Care Products, FDA Products, Car Wash Tunnels & Bay, Cannabis Chemicals, Sporting Goods, Odor Control, Cleaning Chemicals, and Tolling Service
Standorte
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Primäre
13875 Mica St
Santa Fe Springs, California 90670, US
Employees at Ki Liquid Engineering
Aktualisierungen
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QC Manager will be responsible for maintaining QC standards by overseeing the inspection and testing of materials, components, production, and finished products. The QC Manager will lead and manage daily activities to ensure compliance with applicable regulatory, customers and internal requirements. • Knowledge of quality control methods and techniques • Experience in managing a team and leading quality initiatives • Ability to communicate effectively with executives and team members • Directs and coordinates the activities of the quality control function to ensure achievement of company objectives. • Strong analytical and problem-solving skills • Professional certifications in quality control or quality management are a plus • Evaluates current procedures and practices for accomplishing department objectives; develops and implements improvements as needed. • Initiate ISO Certification process. • Directs and coordinates analysis of products in compliance with ISO, Good Manufacturing Practices (GMP), regulations, and SOPs. • Experience in ISO 9001 and other quality management systems • Develops and implements primary quality control systems consistent with ISO, GMP, and SOPs. • Generates protocols, reports, and SOPs, reviews protocols, SOPs, product specifications, and batch records. • Identifies technical problems and develops solutions. • Oversees completion of appropriate documentation to support testing procedures. • Develops and maintains department budget. • Manages laboratory equipment maintenance schedules; ensures laboratory equipment is maintained in accordance with established schedules, and SOPs. • Hires, trains, supervises, motivates, and develops quality control staff; manages schedules and workflow. • Assigns duties and monitors quality of work; assures staff conforms to organizational policies and procedures and government regulations. • Keeps up to date on overall activities of the team, identifying problem areas and taking corrective actions. QUALIFICATIONS: • M.S. in related field and minimum of three years related experience or B.S. in related field and minimum of five years related experience. • Strong knowledge of Private Label Blending/Formulation/Tolling and Bottling manufacturing processes and equipment validation. • ISO, GMP, SOP, and product/process validation. • Thorough knowledge of ISO, GMP, CFR, and factors impacting compliance. • Knowledge of and ability to utilize statistics in evaluation of data. • Thorough knowledge of ISO regulations. • Experience working with equipment manufacturers • Experience with laboratory environment, equipment, and safety procedures. • Excellent written and oral communication skills • Strong organizational, problem-solving, and analytical skills • Ability to manage priorities and workflow • Versatility, flexibility, and a willingness to work within constantly changing priorities with enthusiasm. Email Resume to: [email protected]
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QC Manager will be responsible for maintaining QC standards by overseeing the inspection and testing of materials, components, production, and finished products. The QC Manager will lead and manage daily activities to ensure compliance with applicable regulatory, customers and internal requirements. • Knowledge of quality control methods and techniques • Experience in managing a team and leading quality initiatives • Ability to communicate effectively with executives and team members • Directs and coordinates the activities of the quality control function to ensure achievement of company objectives. • Strong analytical and problem-solving skills • Professional certifications in quality control or quality management are a plus • Evaluates current procedures and practices for accomplishing department objectives; develops and implements improvements as needed. • Initiate ISO Certification process. • Directs and coordinates analysis of products in compliance with ISO, Good Manufacturing Practices (GMP), regulations, and SOPs. • Experience in ISO 9001 and other quality management systems • Develops and implements primary quality control systems consistent with ISO, GMP, and SOPs. • Generates protocols, reports, and SOPs, reviews protocols, SOPs, product specifications, and batch records. • Identifies technical problems and develops solutions. • Oversees completion of appropriate documentation to support testing procedures. • Develops and maintains department budget. • Manages laboratory equipment maintenance schedules; ensures laboratory equipment is maintained in accordance with established schedules, and SOPs. • Hires, trains, supervises, motivates, and develops quality control staff; manages schedules and workflow. • Assigns duties and monitors quality of work; assures staff conforms to organizational policies and procedures and government regulations. • Keeps up to date on overall activities of the team, identifying problem areas and taking corrective actions. QUALIFICATIONS: • M.S. in related field and minimum of three years related experience or B.S. in related field and minimum of five years related experience. • Strong knowledge of Private Label Blending/Formulation/Tolling and Bottling manufacturing processes and equipment validation. • ISO, GMP, SOP, and product/process validation. • Thorough knowledge of ISO, GMP, CFR, and factors impacting compliance. • Knowledge of and ability to utilize statistics in evaluation of data. • Thorough knowledge of ISO regulations. • Experience working with equipment manufacturers • Experience with laboratory environment, equipment, and safety procedures. • Excellent written and oral communication skills • Strong organizational, problem-solving, and analytical skills • Ability to manage priorities and workflow • Versatility, flexibility, and a willingness to work within constantly changing priorities with enthusiasm. Email Resume to: [email protected]
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QC Manager will be responsible for maintaining QC standards by overseeing the inspection and testing of materials, components, production, and finished products. The QC Manager will lead and manage daily activities to ensure compliance with applicable regulatory, customers and internal requirements. • Knowledge of quality control methods and techniques • Experience in managing a team and leading quality initiatives • Ability to communicate effectively with executives and team members • Directs and coordinates the activities of the quality control function to ensure achievement of company objectives. • Strong analytical and problem-solving skills • Professional certifications in quality control or quality management are a plus • Evaluates current procedures and practices for accomplishing department objectives; develops and implements improvements as needed. • Initiate ISO Certification process. • Directs and coordinates analysis of products in compliance with ISO, Good Manufacturing Practices (GMP), regulations, and SOPs. • Experience in ISO 9001 and other quality management systems • Develops and implements primary quality control systems consistent with ISO, GMP, and SOPs. • Generates protocols, reports, and SOPs, reviews protocols, SOPs, product specifications, and batch records. • Identifies technical problems and develops solutions. • Oversees completion of appropriate documentation to support testing procedures. • Develops and maintains department budget. • Manages laboratory equipment maintenance schedules; ensures laboratory equipment is maintained in accordance with established schedules, and SOPs. • Hires, trains, supervises, motivates, and develops quality control staff; manages schedules and workflow. • Assigns duties and monitors quality of work; assures staff conforms to organizational policies and procedures and government regulations. • Keeps up to date on overall activities of the team, identifying problem areas and taking corrective actions. QUALIFICATIONS: • M.S. in related field and minimum of three years related experience or B.S. in related field and minimum of five years related experience. • Strong knowledge of Private Label Blending/Formulation/Tolling and Bottling manufacturing processes and equipment validation. • ISO, GMP, SOP, and product/process validation. • Thorough knowledge of ISO, GMP, CFR, and factors impacting compliance. • Knowledge of and ability to utilize statistics in evaluation of data. • Thorough knowledge of ISO regulations. • Experience working with equipment manufacturers • Experience with laboratory environment, equipment, and safety procedures. • Excellent written and oral communication skills • Strong organizational, problem-solving, and analytical skills • Ability to manage priorities and workflow • Versatility, flexibility, and a willingness to work within constantly changing priorities with enthusiasm. Email Resume to: [email protected]
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QC Manager will be responsible for maintaining QC standards by overseeing the inspection and testing of materials, components, production, and finished products. The QC Manager will lead and manage daily activities to ensure compliance with applicable regulatory, customers and internal requirements. • Knowledge of quality control methods and techniques • Experience in managing a team and leading quality initiatives • Ability to communicate effectively with executives and team members • Directs and coordinates the activities of the quality control function to ensure achievement of company objectives. • Strong analytical and problem-solving skills • Professional certifications in quality control or quality management are a plus • Evaluates current procedures and practices for accomplishing department objectives; develops and implements improvements as needed. • Initiate ISO Certification process. • Directs and coordinates analysis of products in compliance with ISO, Good Manufacturing Practices (GMP), regulations, and SOPs. • Experience in ISO 9001 and other quality management systems • Develops and implements primary quality control systems consistent with ISO, GMP, and SOPs. • Generates protocols, reports, and SOPs, reviews protocols, SOPs, product specifications, and batch records. • Identifies technical problems and develops solutions. • Oversees completion of appropriate documentation to support testing procedures. • Develops and maintains department budget. • Manages laboratory equipment maintenance schedules; ensures laboratory equipment is maintained in accordance with established schedules, and SOPs. • Hires, trains, supervises, motivates, and develops quality control staff; manages schedules and workflow. • Assigns duties and monitors quality of work; assures staff conforms to organizational policies and procedures and government regulations. • Keeps up to date on overall activities of the team, identifying problem areas and taking corrective actions. QUALIFICATIONS: • M.S. in related field and minimum of three years related experience or B.S. in related field and minimum of five years related experience. • Strong knowledge of Private Label Blending/Formulation/Tolling and Bottling manufacturing processes and equipment validation. • ISO, GMP, SOP, and product/process validation. • Thorough knowledge of ISO, GMP, CFR, and factors impacting compliance. • Knowledge of and ability to utilize statistics in evaluation of data. • Thorough knowledge of ISO regulations. • Experience working with equipment manufacturers • Experience with laboratory environment, equipment, and safety procedures. • Excellent written and oral communication skills • Strong organizational, problem-solving, and analytical skills • Ability to manage priorities and workflow • Versatility, flexibility, and a willingness to work within constantly changing priorities with enthusiasm. Email Resume to: [email protected]
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QC Manager will be responsible for maintaining QC standards by overseeing the inspection and testing of materials, components, production, and finished products. The QC Manager will lead and manage daily activities to ensure compliance with applicable regulatory, customers and internal requirements. • Knowledge of quality control methods and techniques • Experience in managing a team and leading quality initiatives • Ability to communicate effectively with executives and team members • Directs and coordinates the activities of the quality control function to ensure achievement of company objectives. • Strong analytical and problem-solving skills • Professional certifications in quality control or quality management are a plus • Evaluates current procedures and practices for accomplishing department objectives; develops and implements improvements as needed. • Initiate ISO Certification process. • Directs and coordinates analysis of products in compliance with ISO, Good Manufacturing Practices (GMP), regulations, and SOPs. • Experience in ISO 9001 and other quality management systems • Develops and implements primary quality control systems consistent with ISO, GMP, and SOPs. • Generates protocols, reports, and SOPs, reviews protocols, SOPs, product specifications, and batch records. • Identifies technical problems and develops solutions. • Oversees completion of appropriate documentation to support testing procedures. • Develops and maintains department budget. • Manages laboratory equipment maintenance schedules; ensures laboratory equipment is maintained in accordance with established schedules, and SOPs. • Hires, trains, supervises, motivates, and develops quality control staff; manages schedules and workflow. • Assigns duties and monitors quality of work; assures staff conforms to organizational policies and procedures and government regulations. • Keeps up to date on overall activities of the team, identifying problem areas and taking corrective actions. QUALIFICATIONS: • M.S. in related field and minimum of three years related experience or B.S. in related field and minimum of five years related experience. • Strong knowledge of Private Label Blending/Formulation/Tolling and Bottling manufacturing processes and equipment validation. • ISO, GMP, SOP, and product/process validation. • Thorough knowledge of ISO, GMP, CFR, and factors impacting compliance. • Knowledge of and ability to utilize statistics in evaluation of data. • Thorough knowledge of ISO regulations. • Experience working with equipment manufacturers • Experience with laboratory environment, equipment, and safety procedures. • Excellent written and oral communication skills • Strong organizational, problem-solving, and analytical skills • Ability to manage priorities and workflow • Versatility, flexibility, and a willingness to work within constantly changing priorities with enthusiasm. Email Resume to: [email protected]
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QC Manager will be responsible for maintaining QC standards by overseeing the inspection and testing of materials, components, production, and finished products. The QC Manager will lead and manage daily activities to ensure compliance with applicable regulatory, customers and internal requirements. • Knowledge of quality control methods and techniques • Experience in managing a team and leading quality initiatives • Ability to communicate effectively with executives and team members • Directs and coordinates the activities of the quality control function to ensure achievement of company objectives. • Strong analytical and problem-solving skills • Professional certifications in quality control or quality management are a plus • Evaluates current procedures and practices for accomplishing department objectives; develops and implements improvements as needed. • Initiate ISO Certification process. • Directs and coordinates analysis of products in compliance with ISO, Good Manufacturing Practices (GMP), regulations, and SOPs. • Experience in ISO 9001 and other quality management systems • Develops and implements primary quality control systems consistent with ISO, GMP, and SOPs. • Generates protocols, reports, and SOPs, reviews protocols, SOPs, product specifications, and batch records. • Identifies technical problems and develops solutions. • Oversees completion of appropriate documentation to support testing procedures. • Develops and maintains department budget. • Manages laboratory equipment maintenance schedules; ensures laboratory equipment is maintained in accordance with established schedules, and SOPs. • Hires, trains, supervises, motivates, and develops quality control staff; manages schedules and workflow. • Assigns duties and monitors quality of work; assures staff conforms to organizational policies and procedures and government regulations. • Keeps up to date on overall activities of the team, identifying problem areas and taking corrective actions. QUALIFICATIONS: • M.S. in related field and minimum of three years related experience or B.S. in related field and minimum of five years related experience. • Strong knowledge of Private Label Blending/Formulation/Tolling and Bottling manufacturing processes and equipment validation. • ISO, GMP, SOP, and product/process validation. • Thorough knowledge of ISO, GMP, CFR, and factors impacting compliance. • Knowledge of and ability to utilize statistics in evaluation of data. • Thorough knowledge of ISO regulations. • Experience working with equipment manufacturers • Experience with laboratory environment, equipment, and safety procedures. • Excellent written and oral communication skills • Strong organizational, problem-solving, and analytical skills • Ability to manage priorities and workflow • Versatility, flexibility, and a willingness to work within constantly changing priorities with enthusiasm. Email Resume to: [email protected]