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Sanofi Global MSAT (Manufacturing Sciences, Analytics and Technology) acts as a crucial link between R& ... Proficient in statistical software such as JMP, SIMCA, Modde, Design Expert, PASS, R, Python.

Sanofi Global MSAT (Manufacturing Sciences, Analytics and Technology) acts as a crucial link between R& ... Proficiency in statistical software and programming languages such as R, Python, JMP, etc. ... In partnership with various functions (Manufacturing 4.0, Digital, M&S, R&D), the MSAT DSD team aims

You will also be a full member of several R&D teams, CMC Sub teams, and R&D SI (Scientific Integrator ... A main objective of the role is strong collaboration with R&D and the commercial manufacturing sites ... Partner with R&D and Supply Chain to identify and implement opportunities for active decrease in COGs ... manufacturing site execution plan per product, in line with the overall strategy as outlined by the R& ... ) Sub teams, working hand in hand with R&D to successfully develop and transfer to the commercial launch

Sanofi Global MSAT (Manufacturing Sciences, Analytics and Technology) acts as a crucial link between R& ... Proficiency in statistical software and programming languages such as JMP, SIMCA, Modde, Design Expert, PASS, R,

Work closely with engineering, manufacturing, and R&D teams to ensure proper qualification of equipment

Managing various stakeholders such as R&D, Manufacturing Operations, SpeCare sites, Finance M&S, Finance

Work closely with engineering, manufacturing, and R&D teams to ensure proper qualification of equipment

For the position as a Mechanical Draftsman you are responsible for: Developing plans: You translate the design prepared by the project engineer into detailed drawings. You ensure an accurate and fully elaborated detailed design Collaboration and consultation: In case of questions, uncertainties, or possible design alternatives, you always coordinate with the project engineer.

Description: Development, implementation and execution of URS, SIA, DQ, IQ, OQ, PQ, RV and TM activities for small scale equipment, including the related software. Develops, implements and executes validation studies for cGMP-critical process systems to demonstrate compliance to cGMP-, User- and Regulatory requirements. Hands-on activity envisaged in relation to this.