Assist the GPH & TT team in the development and execution of scalable, robust processes for arg Substances and drug products. Assist the team Subject Matter Expert in process knowledge transfer for crus Substances and drug products in support of current Good Manufacturing Practices (CGMP) manufacturing.
Assist in the design and technology transfer of MRNA and nanoparticle manufacturing processes by contributing to and reviewing Batch Records/Master Production Records and Standard Operating Procedures. Provide technical support for scale-up and manufacturing issues, and develop solutions to improve process efficiency and product quality. Troubleshoot process/analytical issues in scale-up and in production.
Effectively communicate with cross-functional teams including Analytical Development, R&D, Quality Assurance, Regulatory Affairs, Project Management, and Legal. Assist in the preparation of technical reports and presentations. Contribute to Investigational New Drug filings and regulatory documentation. Assist in training other team members.
Employer permits the employee in this role to work remotely, from their residence within the area of intended employment two days per week. Travel may be required less than 20% to manufacturing sites, including 1-2 trips to manufacturing/company sites abroad in the Netherlands and France.
To apply submit resume to recruiting@sanofi.com with job code #2392. EOE.
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