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Quality & Regulatory Manager at Purus Manufacturing LLC Quality & Regulatory Manager at Purus Manufacturing LLC in Huntington Park, California Posted in 5 days ago.

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full-time About the Role Purus Manufacturing LLC is a dietary supplement manufacturing company based in Northridge, California. We are looking for an experienced Quality & Regulatory Manager to lead our quality and regulatory functions, ensure compliance with applicable industry requirements, and support high standards across our manufacturing operations. This is a full-time, on-site position at our Northridge, California facility. Key Responsibilities Lead and continuously improve the company's Quality Management System (QMS) and overall quality standards. Ensure compliance with applicable FDA regulations, cGMP requirements, and internal quality standards. Oversee Quality Assurance and Regulatory Affairs activities across manufacturing operations. Lead quality investigations, corrective and preventive actions, and continuous improvement initiatives. Ensure products, manufacturing processes, and quality practices consistently meet established regulatory and quality requirements. Lead internal audits and support regulatory inspections and external GMP audits. Oversee supplier quality and qualification programs and ensure appropriate quality oversight of external partners. Provide regulatory guidance for product development, ingredients, labeling, packaging, and related business activities. Lead and develop the Quality & Regulatory team and provide guidance to cross-functional teams. Partner with Production, Operations, Product Development, Supply Chain, and Executive Leadership to support compliance and company growth. Qualifications Bachelor's degree in Chemistry, Biology, Food Science, Microbiology, Quality Assurance, Regulatory Affairs, or a related scientific field. 5-7+ years of progressive experience in Quality Assurance and/or Regulatory Affairs within dietary supplements, pharmaceuticals, food, cosmetics, or another FDA-regulated manufacturing environment. 3+ years of leadership or management experience. Strong knowledge of FDA regulations and cGMP requirements. Proven experience managing quality systems, regulatory compliance, audits, and inspections in an FDA-regulated manufacturing environment. Strong understanding of manufacturing processes, quality standards, and continuous improvement practices. Strong analytical, problem-solving, and decision-making skills. Excellent communication, leadership, and cross-functional collaboration skills. Experience with electronic Quality Management Systems (eQMS) is a plus. What We Offer Competitive salary based on experience and qualifications. Paid vacation and sick leave. 401(k). A key leadership role with direct impact on quality and regulatory operations. Opportunities to contribute to process improvement and company growth.