Quality Systems Specialist (Contract)

One of the leading skincare companies in thee United States is looking to bring on a Quality Systems Specialist to their QA team in their South San Francisco office. The specialist will mainly be responsible for ensuring the Quality Documents, Validation reports, SOP's, Change Control, non-conformance, and document control are following cGMP regulations - and assisting in eQMS system development, validation, and launch activities.

Responsibilities:

• Help generate, organize, manage and archive the cGMP documentation, investigation support documents, non-conformance, product release, CAPA, and stability program.
• Work cross functionally within the organization to ensure the company is in compliance with applicable cGMP requirements and regulatory and Federal regulations.
• Implement eQMS updates as needed to comply with applicable FDA compliance requirements
• Provide training and access to the EQMS system which manages CAPAs, Change Controls and Deviations.
• Review and approve documents for release as the QA SME.

Requirements:

• Up to date cGMP requirements
• 3+ years of experience in quality assurance
• 1-2 years of quality systems experience
• Prior experience in the skincare, pharmaceutical or manufacturing industry

Don't miss your chance to get your foot in the door at a company with proven success!