Sumitomo Chemical: Group Companies of the Americas
Compliance Supervisor - Valent BioSciences, LLC
Sumitomo Chemical: Group Companies of the Americas, Osage, Iowa, United States, 50461
Compliance Supervisor – Valent BioSciences, LLC
Sumitomo Chemical: Group Companies of the Americas, a wholly owned subsidiary of Sumitomo Chemical, is seeking a Compliance Supervisor for its manufacturing site in Osage, IA.
About the Company Valent BioSciences LLC is a worldwide leader in the research, development, manufacturing, and commercialization of biorational products for the agriculture, public health, and forestry markets. With over 60 years of experience, our products are used in sustainable operations across 95 countries, maximizing plant quality, productivity, and sustainability.
Job Description As a Compliance Supervisor, you will ensure the integrity and effectiveness of Valent BioSciences’ quality and compliance systems at the Osage facility. You will oversee a team of Documentation and Compliance Specialists, drive ISO 9001 and ISO/IEC 17025 compliance, manage customer complaint and Material Review Board (MRB) programs, and ensure adherence to regulatory requirements including EPA FIFRA, GLP, and FDA 21 CFR Part 11.
Key Responsibilities
Lead quality and compliance activities including audits, CAPA, and process improvements.
Supervise and mentor Documentation and Compliance Specialists.
Act as Quality Assurance Unit for EPA FIFRA GLP studies, ensuring proper documentation and study integrity.
Review and approve COAs, test records, and product batch release in LIMS and SAP.
Serve as backup to the Sr. Quality Manager, supporting plant-wide quality initiatives.
Electronic Quality Systems Oversight
Manage and maintain LIMS, SAP (Quality functions), and OpenText.
Oversee configuration, validation, access control, and data integrity compliance.
Partner with IT to implement system upgrades, integrations, and training.
Ensure accurate documentation and secure record retention across electronic systems.
ISO 9001 & 17025 Program Management
Maintain and improve the QMS to meet ISO 9001 and ISO/IEC 17025 requirements.
Coordinate audits, management reviews, and CAPA follow‑ups.
Track and report key quality performance indicators.
Facilitate employee training and SOP adherence.
Customer Complaints & MRB Oversight
Manage the customer complaint process from intake to closure.
Lead MRB activities to assess nonconforming materials.
Trend and report complaint and MRB data to identify recurring issues.
Prepare summary reports for management, audits, and regulatory submissions.
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About the Company Valent BioSciences LLC is a worldwide leader in the research, development, manufacturing, and commercialization of biorational products for the agriculture, public health, and forestry markets. With over 60 years of experience, our products are used in sustainable operations across 95 countries, maximizing plant quality, productivity, and sustainability.
Job Description As a Compliance Supervisor, you will ensure the integrity and effectiveness of Valent BioSciences’ quality and compliance systems at the Osage facility. You will oversee a team of Documentation and Compliance Specialists, drive ISO 9001 and ISO/IEC 17025 compliance, manage customer complaint and Material Review Board (MRB) programs, and ensure adherence to regulatory requirements including EPA FIFRA, GLP, and FDA 21 CFR Part 11.
Key Responsibilities
Lead quality and compliance activities including audits, CAPA, and process improvements.
Supervise and mentor Documentation and Compliance Specialists.
Act as Quality Assurance Unit for EPA FIFRA GLP studies, ensuring proper documentation and study integrity.
Review and approve COAs, test records, and product batch release in LIMS and SAP.
Serve as backup to the Sr. Quality Manager, supporting plant-wide quality initiatives.
Electronic Quality Systems Oversight
Manage and maintain LIMS, SAP (Quality functions), and OpenText.
Oversee configuration, validation, access control, and data integrity compliance.
Partner with IT to implement system upgrades, integrations, and training.
Ensure accurate documentation and secure record retention across electronic systems.
ISO 9001 & 17025 Program Management
Maintain and improve the QMS to meet ISO 9001 and ISO/IEC 17025 requirements.
Coordinate audits, management reviews, and CAPA follow‑ups.
Track and report key quality performance indicators.
Facilitate employee training and SOP adherence.
Customer Complaints & MRB Oversight
Manage the customer complaint process from intake to closure.
Lead MRB activities to assess nonconforming materials.
Trend and report complaint and MRB data to identify recurring issues.
Prepare summary reports for management, audits, and regulatory submissions.
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