QA Manager GMP Compliance & CAPA Lead

International Vitamin Corporation; Parkins Lake (SC); On-site; USD 85,000 - 125,000; Full time

Job summary

International Vitamin Corporation (IVC) is seeking a Senior Quality Assurance leader to oversee day-to-day QA operations, audits, document control, GMP training, and SOP development in the production of dietary supplements and related products.

The role requires a Bachelor’s degree in a scientific/engineering field plus 2–5 years of experience, with 5–10 years in quality systems and at least 3 years in a supervisory capacity. Expertise in cGMP guidelines and 21 CFR parts 110/111 is expected.

Qualifications

• Bachelor’s degree in a Scientific or Engineering discipline with exposure to Chemistry, Microbiology, and/or Biology.
• 2–5 years of experience; 5–10 years with supervisory role in quality systems in dietary supplements/pharmaceutical manufacturing.
• Professional quality discipline certifications (CQE, CQA, PCQI) desired.

Responsibilities

• Enforce GMP compliance across the organization and with strategic partners.
• Review and assist in developing the quality system policies and procedures.
• Maintain and implement the company’s quality system policies and procedures.
• Develop, update, and maintain SOPs.
• Lead external audits and coordinate CAPA responses; prepare audit reports and monitor CAPA sustainability.
• Prepare quality reports and discuss quality issues with operations monthly.
• Oversee the GMP squad and collaborate with all departments to ensure program effectiveness.
• Perform additional tasks or special projects as assigned by senior Quality Management.

Skills

Quality management

GMP knowledge

Leadership/ Supervisory

Communication

English proficiency

Education

Bachelor’s degree in a Scientific or Engineering discipline

Exposure to Chemistry, Microbiology, or Biology

Professional quality discipline certifications (CQE, CQA, PCQI) desired

Tools

Microsoft Office

Job description

International Vitamin Corporation (IVC) is seeking a Senior Quality Assurance leader to oversee day-to-day QA operations, audits, document control, GMP training, and SOP development in the production of dietary supplements and related products.

The role requires a Bachelor’s degree in a scientific/engineering field plus 2–5 years of experience, with 5–10 years in quality systems and at least 3 years in a supervisory capacity. Expertise in cGMP guidelines and 21 CFR parts 110/111 is expected.