QC Stability Data Entry 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 seeking a QC Stability Data Entry Specialist to support our Quality Control (QC) team. This position offers hands-on experience in managing and maintaining critical stability data that supports the release, validation, and lifecycle of biopharmaceutical products. The QC group plays a vital role in ensuring data integrity, accuracy, and compliance with regulatory standards for product stability programs.

The ideal candidate will have strong attention to detail, proficiency with data systems, and an understanding of Good Manufacturing Practices (GMP) documentation requirements. This role will support data entry, review, and maintenance of QC stability databases and related documentation.

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

• Enter, verify, and maintain stability data into electronic systems and databases.
• Perform accurate transcription of laboratory data into LIMS or stability tracking systems.
• Support data verification and quality checks to ensure consistency and regulatory compliance.
• Assist in generating stability summary tables, trend charts, and data reports as requested.
• Collaborate with QC analysts, stability coordinators, and QA personnel to resolve data discrepancies.
• Assist with preparation and organization of stability documentation for audits and inspections.
• Support general QC documentation activities, including scanning, archiving, and version control.
• Participate in cross-functional meetings and process improvement initiatives related to data management.
• Collaborate with a mentor team of cross-functional team members as well as the other interns in the class.
• Complete 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, product development, and regulatory approval processes is desirable.
• Good verbal and written communication skills.
• Ability to think creatively and be a team player.

Neurocrine Biosciences is an EEO/Disability/Vets employer.

We are committed to building a workplace of belonging, respect, and empowerment, and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don't line up to exactly what we have outlined in the job description.