Intern QA

Overview

SUMMARY

The Intern will be part of Commercial Manufacturing QA team responsible for the Quality oversight of commercial manufacturing activities associated with Drug substance, Drug Product and primary packaged Product.

He / She will contribute to the maintenance and compliance of Incyte Quality Management System.

Duties and Responsibilities

Coordinate the collection of Annual Product Quality Review data and support the issuance of Annual Product Quality Review Reports, Manage and approve internal and external deviations, OOS and related investigations, Manage and monitor implementation of internal and external change controls, Manage and monitor implementation of internal and external CAPAs, Manage and monitor Product Complaints, Performs all responsibilities in accordance with company policies, procedures, applicable regulations and safety requirements, Cooperate with the Supply Chain, Commercial Operations and Regulatory Affairs functions.

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.

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