Quality Assurance Associate

Solara LaboratoriesMiami Lakesindeedzveřejněno 29. 10. 2026
Nutné:QA/Test

Solara Labs is a growing manufacturer of nutritional supplements dedicated to delivering high-quality, innovative products. We are committed to maintaining the highest standards of quality, safety, and regulatory compliance throughout our manufacturing processes. Overview: We are seeking a highly organized, detail-oriented, and proactive Quality Assurance Associate to join our growing team. The ideal candidate thrives in a fast-paced manufacturing environment, can effectively multitask, and is comfortable managing competing priorities while maintaining accuracy and attention to detail. Key Responsibilities: Conduct inspections of incoming raw materials, packaging components, and finished products to ensure compliance with established specifications. Prepare, review, and maintain quality documentation, including Certificates of Analysis (COAs), product specifications, SOPs, and quality records. Coordinate internal and third-party laboratory testing, review results, and assist with product release activities. Maintain accurate quality records, document control systems, and sample retention inventory. Support compliance with FDA regulations, cGMP requirements, and 21 CFR Part 111. Assist with internal, customer, regulatory, and third-party audits. Participate in investigations involving deviations, out-of-specification (OOS) results, product complaints, and corrective and preventive actions (CAPA). Review product labeling for technical accuracy and regulatory compliance. Collaborate with Production, Quality, and other departments to resolve quality-related issues and support daily operations. Manage multiple assignments and shifting priorities while meeting deadlines and maintaining quality standards. Qualifications: Bachelor's degree in Chemistry, Biology, or a related scientific field, preferred. 3+ years of QA/QC experience in nutraceutical, pharmaceutical, food, or related manufacturing environments preferred. Knowledge of FDA regulations, cGMP, and quality assurance practices. Bilingual: English/Spanish Excellent organizational, multitasking, and time-management skills. Ability to thrive in a fast-paced, deadline-driven environment with changing priorities. Strong attention to detail, accuracy, and documentation skills. Proactive problem-solving skills and the ability to work independently with minimal supervision. Ability to work collaboratively with cross-functional teams. Pay: $50,000.00 - $55,000.00 per year Benefits: 401(k) 401(k) matching Dental insurance Health insurance Life insurance Paid time off Vision insurance Work Location: In person