Quality Assurance Chemist

Huntsman Corporation•Conroe, TX

7d•Onsite

About The Position

Huntsman is seeking an Analytical Quality Chemist supporting the Performance Products Division located in Conroe, Texas. This position will report to the Quality Manager. The Analytical Quality Chemist is responsible for supporting the Conroe manufacturing site through quality systems leadership, analytical chemistry expertise, laboratory operations, and continuous improvement initiatives. This role serves as a subject matter expert for quality management systems, ensuring compliance with ISO 9001:2015 and other regulatory requirements while supporting manufacturing operations through laboratory testing, root cause investigations, risk management activities, and SAP Quality Management (QM) optimization. The position works cross-functionally with Operations, Technical, Quality, and R&D teams to maintain product quality, laboratory excellence, and regulatory compliance.

Requirements

Unrestricted right to work for Huntsman in the United States.
Bachelor of Science degree in Chemistry, Analytical Chemistry, or a related scientific discipline with a minimum of 5 years of relevant experience.
OR Master of Science degree in Chemistry, Analytical Chemistry, or a related scientific discipline with a minimum of 3 years of relevant experience.
Strong knowledge of Quality Management Systems (QMS) and ISO 9001:2015 requirements.
Experience conducting root cause investigations and implementing corrective and preventive actions (CAPA).
Experience working with SAP Quality Management (QM) or similar quality management systems.
Strong wet chemistry laboratory experience.
Proficiency in data analysis, interpretation, and reporting.
Strong mathematical and analytical problem-solving capabilities.
Strong attention to detail and commitment to quality and compliance.
Excellent analytical thinking and troubleshooting abilities.
Strong communication skills with the ability to effectively interact at all organizational levels.
Ability to lead quality initiatives and drive process improvements.
Effective project management and organizational skills.
Strong technical writing and documentation capabilities.
Results-oriented with a proactive approach to issue resolution.
Ability to manage multiple priorities in a dynamic manufacturing environment.
Flexibility and adaptability to changing business priorities.
Strong collaboration and teamwork skills across cross-functional groups.

Nice To Haves

Degree in Analytical Chemistry, Chemistry, or Materials Science.
Strong working knowledge of ISO 14001 environmental management systems.
Experience with Failure Modes and Effects Analysis (FMEA), Root Cause Analysis (RCA), and CAPA programs.
Experience supporting laboratory automation, technology implementation, and digital transformation initiatives.
Knowledge of New Product Introduction (NPI) processes within SAP.
Experience supporting chemical manufacturing operations.
Advanced knowledge of laboratory information systems and data integrity requirements.
Experience leading continuous improvement initiatives within quality and laboratory environments.

Responsibilities

Serve as the site Subject Matter Expert (SME) for quality systems, procedures, and compliance requirements.
Support and maintain the site's Quality Management System (QMS) in alignment with ISO 9001:2015 standards.
Facilitate management reviews, internal audits, external ISO audits, and customer audits.
Develop, implement, and maintain Standard Operating Procedures (SOPs), Work Instructions, Control Plans, and quality documentation.
Lead quality investigations utilizing root cause analysis methodologies such as 5 Whys, Fishbone Diagrams, CAPA, and 8D processes.
Monitor site quality KPIs and trends and present data-driven recommendations to site leadership.
Verify calibration, maintenance, and performance of wet chemistry and analytical laboratory instrumentation.
Troubleshoot analytical methods, instrumentation issues, and out-of-specification laboratory results.
Ensure laboratory testing activities comply with approved methods, procedures, and quality requirements.
Maintain laboratory records and support data integrity within SAP and laboratory systems.
Evaluate and help implement new laboratory technologies, automation tools, and testing methodologies to improve efficiency and accuracy.
Manage and optimize SAP Quality Management (QM) processes, including quality planning, traceability, and New Product Introduction (NPI) support.
Support integration of SAP QM with other business systems to ensure effective quality workflows.
Facilitate and support Failure Modes and Effects Analysis (FMEA) activities in partnership with Quality Engineers.
Participate in Environmental, Health, and Safety (EHS) initiatives and company-required training programs.
Serve as Document Control Manager for quality documentation and records management.