Senior Cmc Reg Consultant Small Molecules Life Cycle H/F - Ividata Life Sciences Levallois-Perret - 92
- Bac +5
- Secteur informatique • ESN
- Exp. + 7 ans
Senior CMC Reg Consultant (Small Molecules Lifecycle).
Mission :
To lead and deliver the post-approval activities across all global markets for commercial small molecule products.
Activities and responsibilities :
- Lead the CMC Regulatory strategy for all post-approval activities of the asset, providing proactive and timely advice to the technical team.
- Manage and deliver all regulatory aspects related to Change Control requests
- Lead and deliver all project management activities to support the CMC post-approval work of the asset to ensure the necessary regulatory documents are delivered in time and with the adequate quality.
- Liaise with the Local Affiliates as needed to develop efficient regulatory strategies to deliver the CMC Dossier in line with country requirements and agreed timelines
- Represent CMC Regulatory across the relevant governance meetings and activities
- Write, review and compile (as needed) all regulatory documents in support of each submission on time and in line with country requirements
- Generate gap analysis and risk management support for each submission as needed
- Identify rate limiting deliverables and interdependencies across the technical and regulatory aspects of the different submissions
- Provide status updates to all stakeholders as needed
- Management of all documents through the document management system
Profile/Experience :
- > 10 year experience in CMC technical roles with at least 5 years working on lifecycle management of small molecule products
- Extensive experience in managing the delivery of post-approval CMC Regulatory activities for small molecules assets globally.
- Proven track record of effective stakeholder management across the lifecycle activities of assets
- Organized and independent
- Ability to manage multiple activities concomitantly
- Degree in Pharmacy or a relevant science/technical subject
- Fluent in English
Mission :
To lead and deliver the post-approval activities across all global markets for commercial small molecule products.
Activities and responsibilities :
- Lead the CMC Regulatory strategy for all post-approval activities of the asset, providing proactive and timely advice to the technical team.
- Manage and deliver all regulatory aspects related to Change Control requests
- Lead and deliver all project management activities to support the CMC post-approval work of the asset to ensure the necessary regulatory documents are delivered in time and with the adequate quality.
- Liaise with the Local Affiliates as needed to develop efficient regulatory strategies to deliver the CMC Dossier in line with country requirements and agreed timelines
- Represent CMC Regulatory across the relevant governance meetings and activities
- Write, review and compile (as needed) all regulatory documents in support of each submission on time and in line with country requirements
- Generate gap analysis and risk management support for each submission as needed
- Identify rate limiting deliverables and interdependencies across the technical and regulatory aspects of the different submissions
- Provide status updates to all stakeholders as needed
- Management of all documents through the document management system
Profile/Experience :
- > 10 year experience in CMC technical roles with at least 5 years working on lifecycle management of small molecule products
- Extensive experience in managing the delivery of post-approval CMC Regulatory activities for small molecules assets globally.
- Proven track record of effective stakeholder management across the lifecycle activities of assets
- Organized and independent
- Ability to manage multiple activities concomitantly
- Degree in Pharmacy or a relevant science/technical subject
- Fluent in English
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