GXP Quality Assurance Intern

Who We Are:

At Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values. We know what it takes to be great, and we are as passionate about our people as we are about our purpose - to relieve suffering for people with great needs.

What We Do:

Neurocrine Biosciences is a leading neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, neuroendocrine and neuropsychiatric disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, endometriosis* and uterine fibroids,* as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders because you deserve brave science. For more information, visit neurocrine.com, and follow the company on LinkedIn, X and Facebook. (*in collaboration with AbbVie)

About the Role:

Neurocrine Biosciences, Inc. (NASDAQ: NBIX) is offering the opportunity to gain Quality Assurance (QA) experience in the world of biotechnology. Our intern program offers exposure to the Veeva Quality Management System, risk management, quality audits, and the refinement and maintenance of key performance and monitoring data sources, indicators and dashboards. Our Quality Assurance team boasts extensive industry expertise and is renowned for its innovative approach and collaborative ethos, offering an enriching environment for professional development.

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Your Contributions (include, but are not limited to):

• Supporting a range of activities, including Risk-Based Vendor Management, Internal/External Audit exposure and Inspection Readiness, Veeva Quality Management System, as well as other quality assurance activities
• Collect and compile historical/current data and develop automated reports for vendor metrics to apply to monthly reports for cross functional and department monitoring /review
• Utilize analytical skills to compile and analyze data from vendor activities, supporting the creation of key performance indicators to enhance proactive vendor management strategies
• Participate in generating reports and presentations to communicate findings and mitigation approaches to stakeholders
• Collaborate on the creation of a staging area for regulatory Inspection Readiness
• Collect and organize program files in support of regulatory inspection readiness
• Scanning and uploading documents and records, as necessary
• Create and/or review training materials, PowerPoint Slides, and workflows diagrams
• Interacting with various Quality and interdepartmental areas within the company
• Completing a special project and present the recommendations to senior management upon completion

Requirements:

• Pursuing an undergraduate degree with an interest in biotechnology
• Prior experience in the pharmaceutical or biotechnology industry would be an asset but is not required
• Familiarity with biopharmaceutical technologies, physical and life sciences, produc