GXP Quality Assurance Intern

Neurocrine Biosciences

About The Position

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.

Requirements

Pursuing an undergraduate degree with an interest in biotechnology
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

Nice To Haves

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

Responsibilities

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