Share Email Opening Title Quality Assurance/Compliance Intern  EOE Statement We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law.   About the Organization AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines, primarily for the treatment of cardiovascular, metabolic, respiratory, inflammation, autoimmune, oncology, infection and neuroscience diseases. AstraZeneca operates in over 100 countries and its innovative medicines are used by millions of patients worldwide. For more information please visit www.astrazeneca.com .   Description At AstraZeneca, our purpose is to push the boundaries of science to deliver life-changing medicines. We believe the best way we can achieve this is to put science at the center of everything we do. It is this commitment that drives our ability to discover, develop and deliver the advancements the world needs in complex and difficult diseases like cancer, heart disease, and diabetes. The Internship will be a 10–12 week summer program. This is a paid, full time (40 hours/week) position at the AstraZeneca manufacturing facility located at 4601 Highway 62 East in Mt. Vernon, IN. Over the course of the summer, each intern will perform department specific day to day activities as assigned by their Mentor (supervisor).  Each intern will also be assigned a key project of which they will be responsible for leading, executing and reporting out on to Site Leadership and staff. Internship Mentors will guide and coach interns throughout the summer. Interns will also have the opportunity to job shadow and participate in various lunch and learns to gain a broad understanding of all functions at the Mt. Vernon site.  Objective: Responsible for providing both tactical and strategic support for Compliance and Quality activities within operations or sites. The core responsibilities of the role are as follows: Support all Compliance programs and execute required Compliance activities to ensure the site meets current GMP requirements of all local/global regulations and internal AZ Quality and Compliance policies.  Also look for opportunities for increase efficiency in the Quality ways of working. Primary Duties: Provide support to Quality Systems processes including but not limited to; Quality Risk Assessments, Complaints, Quality Events / Deviations, CAPA, Change Control, Product Reviews, Supplier Quality, Internal Audit Program, and other Quality Systems as needed to support the site. Drive continuous improvements efforts through monitoring/ evaluation of site systems & processes against current Compliance requirements and influencing key stakeholders on recommended Compliance improvements. Support in managing inspections of site by External Customers, internal assessors, and Regulatory authorities. Data gathering, internal benchmarking, writing/presentation, cost benefit analysis. Executing assigned project & presenting project findings to site leadership and staff at the end of summer.   Position Requirements Rising junior or senior working to obtain a bachelor's degree in engineering or science-related field, or MBA student. Computer systems (e.g., Word, Excel, PowerPoint) knowledge.  Technical writing skills, good communication and influencing skills. Ability to collaborate in multi-disciplinary team. Minimum cumulative GPA 3.0+.       Full-Time/Part-Time Seasonal   Location Mt. Vernon, IN   This position is currently not accepting applications. To search for an open position, please go to http://AstraZenecaPharmaceuticalsInc.appone.com WE ALSO RECOMMEND Other Jobs Within Same Category -- None found -- Other Jobs Within 60 Miles -- None found --

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