GMP Quality Assurance Leader

International Vitamin Corporation; South Carolina; On-site; USD 90,000 - 120,000; Full time

Job summary

International Vitamin Corporation (IVC) seeks a Senior Quality Manager to oversee day-to-day QA operations, audits, document control, and GMP training for dietary supplement production. You will develop SOPs, CAPA responses, and drive continuous improvement to sustain GMP compliance across the organization and partners.

The role requires extensive experience in quality systems, regulatory knowledge (cGMP), and leadership to coordinate cross-functional teams.

Qualifications

• Bachelor’s degree in a related field or equivalent job experience.
• 2-5 years of experience.
• Minimum 5-10 years of experience establishing and maintaining quality systems in the Dietary Supplements and/or pharmaceutical manufacturing industry with 3+ years in a Supervisory role.

Responsibilities

• Enforce GMP compliance in the organization and other 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 the company’s standard operating procedures (SOP’s).
• Participate and/or lead external audits and coordinate CAPA responses; prepare audit reports and monitor sustainability of identified CAPAs.
• Prepare quality reports and conduct monthly meetings with the operations group to discuss quality issues and improvements.
• Oversee the GMP squad and collaborate with all functional departments to ensure effectiveness of the program.
• Perform additional tasks or special projects as assigned senior Quality Management.

Skills

MS Office

cGMP knowledge

English communication

Quality systems development

Education

Bachelor’s degree in related field

Tools

Microsoft Word

Microsoft Excel

Microsoft Access

Microsoft PowerPoint

Job description

International Vitamin Corporation (IVC) seeks a Senior Quality Manager to oversee day-to-day QA operations, audits, document control, and GMP training for dietary supplement production. You will develop SOPs, CAPA responses, and drive continuous improvement to sustain GMP compliance across the organization and partners.

The role requires extensive experience in quality systems, regulatory knowledge (cGMP), and leadership to coordinate cross-functional teams.