QA Compliance Director — GMP & Regulatory Readiness

US PharmaLab Inc.; North Brunswick Township (NJ); On-site; USD 125,000 - 141,000; Full time

Job summary

USPL is seeking an Associate Director, Quality Assurance Compliance to lead GMP/GLP programs and drive regulatory inspection readiness in North Brunswick, NJ.

You will develop and strengthen QA processes, oversee audits, CAPA, and cross‑functional collaboration to ensure sustainable compliance and operational excellence. This exempt role reports to the Vice President of Quality Assurance and requires a hands‑on, strategic QA leader with 10–12 years of industry experience.

Qualifications

• Bachelor’s degree or higher in science or related disciplines.
• About 10-12 years of relevant work experience in dietary supplement, nutraceutical, food, pharmaceutical, or biotech industry with QA/QC experience in Dietary Supplement GMP manufacturing or CDMO environment.
• PCQI certification is required; auditing, FSMA, HACCP or related certifications preferred.

Responsibilities

• Develop and maintain GXP required SOPs and related documents; approve SOPs ensuring control of GXP operations.
• Assist in / or perform periodic reviews of programs including vendor qualification management and annual quality management reviews; assist internal audits.
• Manage customer specifications, COAs, SDS, labels and related technical documents per product development direction.
• Oversee review/approval of Food Safety Plans, validation/verification protocols and related reports.
• Lead audits and provide support during external audits; drive CAPA and corrective actions.

Skills

GXP knowledge

Audit readiness

Leadership

Regulatory compliance

Education

Bachelor’s degree or higher in science

Job description

USPL is seeking an Associate Director, Quality Assurance Compliance to lead GMP/GLP programs and drive regulatory inspection readiness in North Brunswick, NJ.

You will develop and strengthen QA processes, oversee audits, CAPA, and cross‑functional collaboration to ensure sustainable compliance and operational excellence. This exempt role reports to the Vice President of Quality Assurance and requires a hands‑on, strategic QA leader with 10–12 years of industry experience.