QA/QC & Quality Systems Specialist – GMP/CI

Sun Nutraceuticals; Florida; Presencial; USD 55.000 - 85.000; Jornada completa

Descripción de la vacante

Sun Nutraceuticals in Florida seeks a hands-on QA/QC professional to strengthen quality systems in a fast-growing dietary supplement operation compliant with 21 CFR Part 111. This role combines daily QA/QC execution with active Quality Management System development and requires collaboration with Quality leadership to elevate process consistency and inspection readiness.

You will draft and review SOPs, support supplier qualification, drive CAPA effectiveness, manage documentation, and

Formación

• 1+ year in a QA or QC role in dietary supplements or food/beverage.
• Relevant education/training (degree in relevant field, GMP certifications, etc.) demonstrating readiness to perform regulated QA/QC work.

Responsabilidades

• Quality System Continuous Improvement: identify compliance gaps, prioritize improvements, and execute a practical roadmap across documentation, training, supplier qualification, and CAPA.
• Documentation & Record Control: draft, revise, version-control SOPs, WI, forms and logbooks; maintain Master Manufacturing Records and Batch Production Records; support change control.
• Quality Control Operations: perform/coordinate receiving inspections, in-process checks, line clearance, label reconciliation, and finished product release/quarantine.
• Supplier & Material Qualification: maintain the Approved Supplier List; collect/assess questionnaires, audits, and performance data.
• Deviations, Investigations & CAPA: log/investigate deviations/OOS/OOT and drive CAPA; track trends and preventive actions.

Conocimientos

QA/QC experience

GMP training

Excel/Sheets

SOP documentation

Educación

Degree in relevant field

GMP certifications

Herramientas

ERP/MRP systems

Descripción del empleo

Sun Nutraceuticals in Florida seeks a hands-on QA/QC professional to strengthen quality systems in a fast-growing dietary supplement operation compliant with 21 CFR Part 111. This role combines daily QA/QC execution with active Quality Management System development and requires collaboration with Quality leadership to elevate process consistency and inspection readiness.

You will draft and review SOPs, support supplier qualification, drive CAPA effectiveness, manage documentation, and