We are recruiting for a Quality Assurance Specialist to support our continued growth and on-going development projects. Qualified individuals need to have the capability, and desire to work with both the development of therapeutics (cGMP) and discovery research (non-cGMP) products and tools to support our innovative work. In this critical role you'll ensure implementation of Quality Management Systems and compliance with applicable regulations and guidelines, while reviewing records for accuracy and consistency with SOP’s. In addition, you will support quality operations through review of documents and records, maintaining data integrity, disposition of materials, and providing cross functional Quality Assurance support. If you aspire to be a critical resource in creating and maintaining a culture of quality, compliance, and cost initiatives, we offer an exceptional and unique opportunity to fully develop your career potential.
Essential Responsibilities
Required Skills and Education
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