GXP Quality Assurance Intern

Posted 9 Days Ago
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San Diego, CA
Internship
Healthtech • Biotech • Pharmaceutical
The Role
As a GXP Quality Assurance Intern at Neurocrine Biosciences, you will support activities related to risk management, internal audits, and KPI development. Tasks include data collection and analysis, report generation, collaboration for regulatory readiness, and special projects. The internship offers exposure to the biopharmaceutical field within a supportive team environment.
Summary Generated by Built In

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, but few options.

What We Do:

Neurocrine Biosciences is a neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs, but few options. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, endocrine and psychiatric disorders. The company’s diverse portfolio includes FDA-approved treatments for tardive dyskinesia, Parkinson’s disease, endometriosis* and uterine fibroids*, as well as clinical programs in multiple 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. *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 risk management, quality audits, and development of key performance 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 Audits and Inspection Readiness, as well as other quality assurance activities.  

  • Collect and compile historical and current data to metrics for vendors to apply to monthly reports for cross functional department 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. 

  • Interacting with various 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, product development, and regulatory approval processes is desirable 

  • Interest and familiarity with various data analytics tools, including Power BI or SQL are a plus 

  • Good verbal and written communication skills  

  • Ability to think creatively and be a team player  

  • Offer flexibility with a willingness to work on multiple projects simultaneously  

  • Bring to the Company a skill set complementary to its technology and development therapeutics 

  • Interest in attending various program events, including social gatherings, career development workshops, and more 

  • Ability to commit to a 10-week, full-time summer program 

Neurocrine Biosciences is an EEO/AA/Disability/Vets employer.

We are committed to building a diverse, equitable, and inclusive workplace, 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.

Top Skills

Power BI
SQL
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The Company
HQ: San Diego, CA
1,150 Employees
On-site Workplace
Year Founded: 1992

What We Do

Neurocrine Biosciences is a neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs, but few options. 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, Parkinson’s disease, endometriosis* and uterine fibroids* , as well as clinical programs in multiple 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.

Review our Community Guidelines: https://bit.ly/3L8M8hx

*in collaboration with AbbVie

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