Quality Assurance Specialist

Cosmetic Solutions•Boca Raton, FL

11d

About The Position

Cosmetic Solutions is a leader in the development and manufacturing of scientifically proven, innovative personal care products. With a focus on face, body, hair, OTC, and professional use formulations, we create some of the most cost effective, high quality and powerful products on the market. Providing world class services to up and coming businesses, large established brands, physicians, estheticians and other skin care professionals; we specialize in research & development, custom formulation, graphic design, manufacturing, packaging and delivery.

Requirements

Previous experience working in a manufacturing environment, preferably in a regulated industry (e.g., pharmaceuticals, medical devices, food).
Strong understanding of Good Manufacturing Practices (GMP) and regulatory requirements (e.g., FDA, ISO).
Experience with quality systems management, CAPAs, deviations, document control, and SOPs.
Excellent analytical and problem-solving skills.
Effective communication and collaboration abilities.
Must be able to read, write, and speak in English.
Detail-oriented with a commitment to quality and compliance.

Responsibilities

Ensure Compliance with GMP regulations throughout the manufacturing process.
Conduct regular audits and inspections to verify adherence to GMP standards.
Develop and implement strategies to continuously improve GMP compliance.
Maintain and improve the company’s quality management system (QMS).
Identify areas for process improvement and implement effective quality control measures.
Collaborate with cross-functional teams to ensure alignment with quality objectives.
Lead investigations into quality issues and non-conformances.
Develop CAPA plans to address root causes and prevent recurrence of quality issues.
Monitor and track the implementation of CAPAs to ensure effectiveness.
Investigate deviations from established procedures and specifications.
Develop and implement corrective actions to address deviations and prevent recurrence.
Ensure the accuracy, completeness, and integrity of quality-related documentation.
Manage document change control processes and maintain document repositories.
Lead root cause investigations for quality issues and customer complaints, implementing corrective and preventive actions.
Work cross-functionally with sales, manufacturing and supply chain teams to address quality concerns that could affect customer satisfaction or regulatory compliance.
Enter scanned work orders into the tracking system.
Review batch cards and log into tracker.
Review finished goods work orders and update tracker.
Send finished goods (FG) samples to the laboratory.
Print and review finished goods work orders.
Attach green status stickers to bulk material.
Review and approve labels for work orders.
Verify that all work orders include the required SDS documentation.
Review the production schedule for accuracy and updates.
Develop, review, and update SOPs to reflect current best practices and regulatory requirements.
Ensure SOPs are consistently followed throughout the organization.
Provide training and support to employees on SOPs and quality processes.
Over time, the Quality Assurance Specialist will develop into a Subject Matter Expert (SME) and assume ownership of key Quality Systems programs in alignment with 21 CFR Parts 210/211. Core areas include Annual Product Reviews (APR/PQR), Supplier Qualification, eQMS administration and internal audit/inspection readiness. The role is expected to drive continuous improvement through quality metrics trending, training support, and ensuring sustained GMP compliance across operations.