Intern - GMP Quality Assurance

Overview INTERNSHIP SUMMARY The Intern will be part of the Commercial Manufacturing QA team responsible for the Quality oversight of commercial manufacturing activities associated with Drug substances, Drug Products and primary and secondary packaged Products. He / She will contribute to the maintenance and compliance of Incyte Quality Management System. Duties And Responsibilities Implement Quality & Technical Agreements (QTA) templates for Commercial Manufacturing activities matching. Coordinate the collection of CMOs Annual Product Quality Review (APQR) reports and support the issuance of Incyte APQR Reports. Support vendor management activities such as update of Veeva Organizations and collection of vendor statements. Review and harmonize classification of QA related documents in eDMS. Support the collection of SM vendor batch documentation to prepare Incyte batch disposition. Support the management and monitoring of Supplier Change Notification (SCN). Support the management and monitoring of internal and external CAPAs. Support the management and monitoring of Product Complaints. Perform all responsibilities in accordance with company policies, procedures, applicable regulations and safety requirements. Cooperate with the Supply Chain, Commercial Operations, Regulatory Affairs, Small Molecule Clinical Manufacturing QA and Biologics Manufacturing QA functions. Contribute positively to a strong culture of business integrity and ethics. Act within compliance and legal requirements as well as within company guidelines. Requirements Student in Master degree in Chemistry, Biology or Pharmacy or equivalent, Partial to full time six month internship (80 - 100 %), Good Organizational and communication skills, diplomacy, and commitment, Demonstrate ability to write technical documents, English fluency written and B2 spoken (the company language), French is an asset. Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required. We Respect Your Privacy Learn more at: http://www.incyte.com/privacy-policy The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate. During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process here. You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work. You can learn more about Incyte’s data protection practices here. By accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incyte’s data protection officer, and your supervisory authority (if applicable). Please contact privacy@incyte.com if you have any questions or concerns or would like to exercise your rights.

Biopharmaceutical company discovering and developing small molecule drugs in oncology and inflammation. Headquartered in Wilmington, DE.

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