Keystone & Golden, Inc.
Vice President of Quality Nutraceuticals
Keystone & Golden, Inc., Phoenix, Arizona, United States, 85003
Overview
Our client — a leading manufacturer in the nutraceutical and dietary supplement industry — is seeking an experienced
Vice President of Quality & Regulatory Affairs
to oversee all aspects of
Quality Assurance, Quality Control, and Regulatory Compliance
across multiple manufacturing and packaging facilities. The ideal candidate is a hands-on, strategic leader who combines technical expertise in FDA-regulated manufacturing with proven experience leading high-performing teams, implementing GMP systems, and ensuring product integrity across global markets. Key Responsibilities
Lead and direct all
Quality Assurance (QA), Quality Control (QC), and Regulatory Affairs (RA)
functions for the organization. Develop, implement, and manage a
comprehensive Quality Management System (QMS)
aligned with
FDA, NSF, TGA, and ISO
standards. Oversee
cGMP compliance , documentation, audits, validations, and continuous improvement initiatives. Serve as the company’s
primary liaison with FDA, NSF, and other regulatory agencies
during inspections and audits. Manage
CAPA programs, supplier qualification , and internal audit systems to ensure consistent manufacturing performance. Oversee
regulatory submissions , including
labeling, claims substantiation, product registration, and international documentation . Collaborate cross-functionally with
R&D, Operations, Supply Chain, and Marketing
to ensure new product development aligns with compliance and quality standards. Build, mentor, and lead multi-site QA/QC and Regulatory teams to achieve operational excellence and continuous improvement. Develop and monitor
department KPIs , ensuring accountability and performance across all quality functions. Qualifications
Bachelor’s degree in
Chemistry, Biology, Engineering, or related scientific discipline
(Master’s preferred). Minimum of
15 years of progressive experience
in
Quality and Regulatory leadership
within
nutraceuticals, dietary supplements, food, or pharmaceutical manufacturing . Strong knowledge of
21 CFR Parts 111, 117, 101, 210/211 , and
ISO 9001 . Demonstrated success managing
FDA and third-party audits
with a record of zero major observations. Proven experience building and managing multi-site teams and implementing scalable QMS frameworks. Excellent communication and leadership skills with the ability to influence at all organizational levels. ASQ Certification (CQA, CQE, or CMQ/OE) strongly preferred. Why Join
Opportunity to lead a best-in-class
Quality & Regulatory organization
in a rapidly growing nutraceutical company. Strategic executive role with influence over product quality, safety, and innovation. Collaborative culture that values science, transparency, and continuous improvement. Competitive compensation, benefits, and long-term growth potential.
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Our client — a leading manufacturer in the nutraceutical and dietary supplement industry — is seeking an experienced
Vice President of Quality & Regulatory Affairs
to oversee all aspects of
Quality Assurance, Quality Control, and Regulatory Compliance
across multiple manufacturing and packaging facilities. The ideal candidate is a hands-on, strategic leader who combines technical expertise in FDA-regulated manufacturing with proven experience leading high-performing teams, implementing GMP systems, and ensuring product integrity across global markets. Key Responsibilities
Lead and direct all
Quality Assurance (QA), Quality Control (QC), and Regulatory Affairs (RA)
functions for the organization. Develop, implement, and manage a
comprehensive Quality Management System (QMS)
aligned with
FDA, NSF, TGA, and ISO
standards. Oversee
cGMP compliance , documentation, audits, validations, and continuous improvement initiatives. Serve as the company’s
primary liaison with FDA, NSF, and other regulatory agencies
during inspections and audits. Manage
CAPA programs, supplier qualification , and internal audit systems to ensure consistent manufacturing performance. Oversee
regulatory submissions , including
labeling, claims substantiation, product registration, and international documentation . Collaborate cross-functionally with
R&D, Operations, Supply Chain, and Marketing
to ensure new product development aligns with compliance and quality standards. Build, mentor, and lead multi-site QA/QC and Regulatory teams to achieve operational excellence and continuous improvement. Develop and monitor
department KPIs , ensuring accountability and performance across all quality functions. Qualifications
Bachelor’s degree in
Chemistry, Biology, Engineering, or related scientific discipline
(Master’s preferred). Minimum of
15 years of progressive experience
in
Quality and Regulatory leadership
within
nutraceuticals, dietary supplements, food, or pharmaceutical manufacturing . Strong knowledge of
21 CFR Parts 111, 117, 101, 210/211 , and
ISO 9001 . Demonstrated success managing
FDA and third-party audits
with a record of zero major observations. Proven experience building and managing multi-site teams and implementing scalable QMS frameworks. Excellent communication and leadership skills with the ability to influence at all organizational levels. ASQ Certification (CQA, CQE, or CMQ/OE) strongly preferred. Why Join
Opportunity to lead a best-in-class
Quality & Regulatory organization
in a rapidly growing nutraceutical company. Strategic executive role with influence over product quality, safety, and innovation. Collaborative culture that values science, transparency, and continuous improvement. Competitive compensation, benefits, and long-term growth potential.
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