|Listed on:||5th June|
|Contact Name:||Jakub Rurkowski|
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Global Regulatory CMC - 6 months Global Regulatory CMC - 6 months The work location is based in Stockley Park on 6-months contact duration Degree in Scientific Discipline (Masters or higher preferred) with 5-7 years in the pharmaceutical industry or in CRO, including at least 3 years CMC regulatory experience Responsibilities will include, but are not limited to, the following: 1. Participate in the development of the CMC regulatory strategy for submissions with an emphasis on international regions. These submissions include CTA/MAA regulatory filings. 2. Collaborate with Regulatory CMC project leads and other relevant line functions to prepare CMC submission documents, registration dossiers, and responses to health authorities for responsible regions. 3. Participate in the regulatory evaluation of CMC change controls by liaising with Regulatory CMC project leads and Regulatory Affairs International to determine regulatory impact for responsible regions. 4. With supervision, will be responsible for the management of Regulatory CMC activities related to commercial compounds for responsible regions. 5. Represent Regulatory CMC on Regulatory Affairs International teams. 6. Participate in document review meetings and discussions for responsible regions. 7. Develop internal knowledge base for CMC international activities including submission document requirements and working practice for interacting with country affiliates. Skills/Knowledge Required: