Larson Maddox
Associate Director, Regulatory Scientific & Quality Affairs
Larson Maddox, Des Moines, Iowa, United States, 50319
Associate Director, Regulatory Scientific & Quality Affairs
A global leader in ingredient innovation is seeking a senior regulatory and quality professional to oversee compliance and strategy for its health‑focused product portfolio. This organization operates across multiple regions and is committed to advancing food, feed, and health solutions through science‑driven approaches.
Base pay range $180,000.00/yr - $180,000.00/yr
Key Responsibilities
Lead and set strategic direction for Regulatory Affairs and Quality Assurance within the business unit.
Develop and manage departmental budgets and strategies aligned with overall business objectives.
Ensure compliance of products, labels, packaging, and marketing materials with global regulatory standards.
Serve as the primary liaison with regulatory authorities and oversee global approval processes.
Drive quality programs including HACCP, GMP, audits, certifications, and customer compliance initiatives.
Qualifications
Bachelor's degree with 10+ years of experience in dietary ingredients, nutraceuticals, or food ingredients; or advanced degree with 5+ years in similar fields.
Strong knowledge of U.S. and global regulatory frameworks (EU, Canada, Brazil, APAC, etc.).
Expertise in Quality Management Systems (GMP, ISO, HACCP) and regulatory dossier preparation.
Proven leadership experience managing teams and cross‑functional projects.
Excellent communication, organizational, and relationship‑building skills.
Seniority level Director
Employment type Full‑time
Job function
Management
Pharmaceutical Manufacturing
#J-18808-Ljbffr
Base pay range $180,000.00/yr - $180,000.00/yr
Key Responsibilities
Lead and set strategic direction for Regulatory Affairs and Quality Assurance within the business unit.
Develop and manage departmental budgets and strategies aligned with overall business objectives.
Ensure compliance of products, labels, packaging, and marketing materials with global regulatory standards.
Serve as the primary liaison with regulatory authorities and oversee global approval processes.
Drive quality programs including HACCP, GMP, audits, certifications, and customer compliance initiatives.
Qualifications
Bachelor's degree with 10+ years of experience in dietary ingredients, nutraceuticals, or food ingredients; or advanced degree with 5+ years in similar fields.
Strong knowledge of U.S. and global regulatory frameworks (EU, Canada, Brazil, APAC, etc.).
Expertise in Quality Management Systems (GMP, ISO, HACCP) and regulatory dossier preparation.
Proven leadership experience managing teams and cross‑functional projects.
Excellent communication, organizational, and relationship‑building skills.
Seniority level Director
Employment type Full‑time
Job function
Management
Pharmaceutical Manufacturing
#J-18808-Ljbffr