Location: Rayong, Thailand Reporting to: Assistant Manager, Sustaining Engineering (based onsite) Summary - To lead process improvement and quality sustaining actions to ensure quality consistency - Required to conduct investigation problem solving, root cause analysis, initiate process control and provide technical support to production - To plan, lead and implement continuous quality improvement projects, Value Improvement Project and Product transfer both locally and abroad Job Description - To lead, support and take actions to production operation in maintaining glove quality consistency - Working with stakeholders to investigate quality issues, implement process control plans and recommend corrective and preventive actions to avoid recurrence of issues and apply Smart Solve system for managing Nonconformances (NCs) - To analyze defective and potential root cause and records in database for statistical analysis and sharing with team to guide corrective and preventive actions - To perform problem solving and root cause analysis through 6 sigma tools, Process Characteristic CTQ and DMAIC (define, measure, analyze, improve and control) - Lead and support continuous process improvement and optimization initiatives such as reduction in glove powder, protein, barrier, and visual defects - Lead and support value improvement projects to reduce product and operational cost - Achieve assigned ADP (annual deployment plan) goals - Provides technical solutions to production, to ensure conformance to quality and regulatory requirements - Conduct change development plan (CDP), Installation qualification, operational qualification, and performance qualification for Forming and/ or Chlorination follow 1QMs system - Perform other related duties of similar type and work on assigned - Perform lab evaluations as required - Emphasize company environment health and safety rules and regulations to employees and ensure compliance - Ensure that all accidents & near miss are reported to management and injured are given proper treatment - Investigate all accidents & near miss and make necessary reports and recommendations - Take disciplinary action on any safety violation in consultation with safety officer and or Human Resource Manager Qualifications & Experience - Bachelor’s degree in chemical engineering, Polymer Science, Chemistry or related fields - At least two years’ experience in Process Engineering within manufacturing environment - Prior experience in medical industry is advantageous - Experience from Gloves Industry preferred - Computer literacy - Self-motivation, team spirit and strong leadership - Native Thai and professional English (verbal and written) skill is required Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law. To read and review this privacy notice click here
Location: Nakorn Pathom, Thailand (5 days' work week based at manufacturing site) Type of medical device portfolio: Safe Saf Access Infusion set, Suction tubing, Drainage bag, Enteral feeding, Connecting tube. Type of raw materials: PVC resin, Component, Packaging. Reporting to: Manager, Quality Management (based onsite) THE COMPANY and BUSINESS Headquartered in Dublin, Ohio, Cardinal Health, Inc. (NYSE: CAH) is a distributor of pharmaceuticals and specialty products; a global manufacturer and distributor of medical and laboratory products; an operator of nuclear pharmacies and manufacturing facilities; and a provider of performance and data solutions. Working to be healthcare’s most trusted partner, our customer-centric focus drives continuous improvement and leads to innovative solutions that improve the lives of people every day. Summary - Leading/Support improvements to quality and resolution of daily quality issues that result in reduced quality issues. - Using a systematic approach to managing quality improvements and resolution of daily quality issues. Support product and process validations. - Support the development and design transfer of new products using Advanced Quality Planning. - Driving continuous improvement activities for product related quality in production floor. Job Description - Quality Engineering is responsible for raw material and service quality planning, evaluation, and control. - Identifies supplier risk levels and completes supplier qualification requirements with related records. - Reviews the process to qualify raw materials and components used in Finished Good Products with cross-functional teams to ensure information is adequate for all requirements and expectations. - Partners with suppliers to manage supplier performance. - Works cross-functionally internally and suppliers in the development and implementation of prevention-based methodologies used in manufacturers, test, providing data. - Demonstrates strong understanding of quality principles, systems, methods, tools, and standards. - Develop and implement quality programs, including tracking, analyzing, reporting and problem solving. - Plans, controls, and assures raw material and process quality in accordance with quality requirements. - Demonstrates knowledge of reliability, maintainability, and risk management. - Apply problem solving and quality improvement tools and techniques, including preventative and corrective actions and how to overcome barriers to quality improvements. - Acquires and analyzes data using appropriate standard quantitative methods to facilitate process analysis and improvements. - Ongoing monitoring and drive quality performance in production processes to meet quality goals. - Ensure compliance of QMS and identify the issue and follow up through CAPA Process. - Support risk analysis and risk management as required. - Using a systematic approach to managing quality improvements and resolution of daily quality issues. Support product and process validations. - Support the QMS audit process. - Performs other related duties of similar type and work on assigned. - Emphasize company environment health and safety rules and regulations to employees and ensure compliance. Qualifications & Experience - Bachelor’s degree in Science or Engineering (Quality Engineering background preferred). - At least 4 years’ experience in quality improvement related field. experience with ISO 13485 or equivalent quality management standards as a preferred qualification - Familiar with quality principles, methods, tools for problem solving and quality improvement programs, FMEA which may include but not limited to tracking, analyzing, reporting and tools and techniques. - Familiar with statistical analysis tools for data analysis. - Computer literacy in Microsoft Word, PowerPoint and Excel. - Expert in Excel i.e. graphs, Power BI, VLOOKUP etc. - A comprehensive understanding of quality processes, manufacturing operations and control procedures within manufacturing operations is required. - High attention to detail and able to propose proactive solutions. - Able to prioritize, plan, coordinate and influence stakeholders across various departments within the manufacturing site. - Versatility, flexibility, and a willingness to work within a constantly changing environment. - Strong leadership, team player and well organized. - Native Thai and good command of business English. Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply. Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law. To read and review this privacy notice click here
What Administration contributes to Cardinal Health Business & Administrative Support is responsible for assisting general business operations by providing an array of administrative and data support activities. Administration is responsible for performing a variety of administrative activities in support of their assigned work team. May assist executives in budget preparation, record maintenance, and generating reports regarding operations, personnel changes, etc. Uses company software to compile and generate reports, statistics, timelines, tables, graphs, correspondence and presentations. May design processes to enhance work flow. Serves as administrative liaison with others within and outside the company regarding administrative issues. Qualifications - 3-6 years of experience, preferred - High School Diploma, GED or equivalent work experience, preferred What is expected of you and others at this level - Effectively applies knowledge of job and company policies and procedures to complete a variety of assignments - In-depth knowledge in technical or specialty area - Applies advanced skills to resolve complex problems independently - May modify process to resolve situations - Works independently within established procedures; may receive general guidance on new assignments - May provide general guidance or technical assistance to less experienced team members Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply. Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law. To read and review this privacy notice click here
Location: Rayong, Thailand Reporting to: Manufacturing Engineering Assistant Manager Summary - Lead material characterization activities to establish material specifications and testing requirements following CTQ principles. - Provide technical expertise in material improvement, validation, and technology scale-up, including new material development and alternate source qualification. - Collaborate with R&D and Packaging Technology teams to ensure full understanding of material characteristics, usage impact, and testing requirements. Job Description - Lead new material development projects and alternate material/source qualification to support business continuity and cost improvement. - Conduct laboratory trials for new or alternative materials and provide study results to support feasibility studies and validation protocols. - Collaborate with universities, research institutes, and external partners to advance material technologies and establish material specifications and test requirements. - Coordinate with Packaging Technology to understand new packaging technologies related to materials and machinery. - Work closely with R&D, Packaging Technology, and Purchasing to define material specifications and testing requirements for new materials. - Provide technical support for material-related issues and participate in MRB evaluations when required. - Monitor key material property trends, conduct correlation studies with product quality, and recommend appropriate actions. - Support VIP projects and other strategic initiatives related to material science. - Support additional tasks related to the role as needed. - Ensure compliance with company GMP, safety, and EHS standards. Qualifications & Experience - Bachelor’s degree in Chemical Engineering, Polymer Science, Chemistry, or a related field. - Minimum 3 years of manufacturing engineering experience; experience in glove manufacturing is advantageous. - Strong technical competence in material development, validation, and process optimization. - Experience in process development, optimization, DOE, correlation studies, and experimental design. - Proficiency in statistical analysis tools such as Minitab, JMP, SPSS or similar statistical software. - Knowledge of FDA medical device validation requirements is preferred. - Strong leadership and problem-solving skills with the ability to work effectively across cross functional teams. - Excellent teamwork, coordination, and interpersonal skills. - Native Thai and advance English skills (written, verbal and presentation skills). Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply. Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law. To read and review this privacy notice click here