Commercial Quality Systems Lead — Product Release

Galderma; Miami (FL); On-site; USD 85,000 - 106,000; Full time

Benefits offered by this job

Medical, dental, and vision coverage

401(k) with company match

Paid time off

Job summary

Galderma is seeking a Senior Specialist, Commercial Quality Systems to lead the quality review, disposition, and release of Rx, OTC, and Cosmetic products marketed in the United States. You will collaborate across CMOs, contract labs, suppliers, and logistics partners to ensure product quality and regulatory compliance.

The role supports QMS processes, supplier quality activities, product complaints investigations, audit readiness, and continuous improvement aligned with FDA regulations and

Qualifications

• Bachelor's Degree in Life Sciences, Biology, Chemistry, Pharmacy, Engineering, or a related scientific discipline required.
• 8+ years of progressive experience within Quality Assurance, Quality Systems, Compliance, Supplier Quality, or related quality function in a regulated industry.
• Experience working with external manufacturers, contract laboratories, and suppliers.
• Experience with electronic Quality Management Systems (eQMS).
• ASQ Certified Quality Auditor (CQA), Certified Quality Engineer (CQE), or equivalent certification preferred.

Responsibilities

• Quality review, disposition, and release of Rx, OTC, and Cosmetics products.
• Support root cause investigations and CAPAs.
• Maintain release metrics and continuous improvement of release processes.
• Support supplier qualification, onboarding, and supplier audits.
• Assist in quality records review and training compliance.

Skills

Quality Assurance

Regulatory knowledge

GxP compliance

Root cause analysis

Vendor management

Education

Bachelor's Degree in Life Sciences or related

Tools

Veeva

TrackWise

MasterControl

SAP

Job description

Galderma is seeking a Senior Specialist, Commercial Quality Systems to lead the quality review, disposition, and release of Rx, OTC, and Cosmetic products marketed in the United States. You will collaborate across CMOs, contract labs, suppliers, and logistics partners to ensure product quality and regulatory compliance.

The role supports QMS processes, supplier quality activities, product complaints investigations, audit readiness, and continuous improvement aligned with FDA regulations and