Quality Compliance & Regulatory Affairs Lead

JAK Diversified II INC; New Jersey; On-site; USD 110,000 - 150,000; Full time

Job summary

Truvant Health and Beauty seeks a QA Compliance & Regulatory Affairs Manager to lead the QMS and ensure FDA/cGMP and customer standards compliance. Responsibilities include deviations, CAPAs, change controls, audits, document control, training, supplier qualification, and continuous improvement initiatives.

The role oversees QA systems and QA training to ensure documentation practices, training programs, and compliance records are maintained, supporting new client onboarding, product launches,

Qualifications

• Minimum 5 years in Nutritional Supplement, Vitamin, or OTC Drug industry.
• FDA cGMP regulations knowledge (21 CFR Parts 210, 211, 111, 117).
• Hands-on experience supporting quality systems, deviations, CAPAs, audits, and regulatory compliance.

Responsibilities

• Maintain and manage the Quality Management System (QMS).
• Oversee deviations, CAPAs, change controls, internal audits, and document control.
• Lead supplier qualification, inspections readiness, and audits.

Skills

Quality systems

Regulatory compliance

CAPA

Internal audits

SOP oversight

Education

Bachelor's degree in science

Tools

Microsoft Excel

Job description

Truvant Health and Beauty seeks a QA Compliance & Regulatory Affairs Manager to lead the QMS and ensure FDA/cGMP and customer standards compliance. Responsibilities include deviations, CAPAs, change controls, audits, document control, training, supplier qualification, and continuous improvement initiatives.

The role oversees QA systems and QA training to ensure documentation practices, training programs, and compliance records are maintained, supporting new client onboarding, product launches,