Mat. & Doc. Flow Manager

Job title: Mat. & Doc. Flow Manager

• Work Mode: Hybrid

• Location : Hyderabad

About the job

Our Team:

The CMC (Chemistry, Manufacturing, and Controls) Demand and Supply Hub serves as the critical link between product development and market delivery, ensuring seamless coordination of supply chain activities to meet patient needs worldwide. We transform scientific innovation into reliable, high-quality pharmaceutical supply through strategic planning and operational excellence.

Main responsibilities:

• The mission of the CMC Material & Documentation Flow Platform is to support the efficient coordination of Drug Product (DP) and Marketed Products (MP) transfer and receipt to sustain clinical and non-clinical development.

• Projects & scope: All products under the responsibility of the CMC Integrated Demand & Supply team

• Supports CMC Integrated Demand and Supply team in the management of material and documentation requirements for shipment and receipt of products (drug products or marketed products) under the accountability and supervision of / and the timelines defined by Demand &Supply Leader assigned to a given project. This includes Providing Material Flow Management (MFM) services: Create and maintain material codes in ERP systems

• Execute ERP transactions (Purchase Orders and Transfers Orders), Coordinate Drug product transfer from manufacturing facilities to packaging facilities

• Oversee Drug Product (DP) flow management for Contract Manufacturing, Organization (CMO) Packaging, Coordinating and execute Drug Product destruction plans

• Provide technical support for Qualipso events management (including CMO/FSO) (e.g.,temperature excursion management, deviation handling)

• Filling product documents such as (but not limited to): Product Information Document (PID), Drug Product Study Document (DPSD), Traceability reports, Technical Conditions for DP shipments.

• Filling products data in D&S tools such as (but not limited to) COMPASS, Demand Owner Module, RDPM, Request product documents to the appropriate owners as prerequisites for DP handling

• such as (but not limited to) TOR, quarantine and shipment authorization, CoR/CoA, Provide support in documentation management in compliance with regulatory requirements: US customs documentation, CN customs requirements definition, French Import License request form preparation and tracking

• Support operational planning activities by providing DP schedule information to CSC

About you

• Experience:  At least 2 years of work experience in supply chain, CMC, clinical fields, pharma R&D, Good Knowledge of Global Exports and Imports is a plus.

• Good communication skills,Ability to work in a Global Team environment

• Knowledge on Process Mapping and Continuous Improvement

• Strong knowledge of Pharma Product Manufacturing/Packaging

• Strong knowledge of CMC and Clinical Supply Chain processes and deliverables

• Strong knowledge of ERP systems,Excellent oral and written communication skills

• Proficiency in written and spoken English is required to interact with multiple interfaces worldwide,

• Good to have spoken and written proficiency in French but it's not a must.

• Ability to work productively with a broad and diverse group of stakeholders, Ability to prioritize task

• Education: Bachelor of Science (BS) degree with supply chain, CMC, clinical fields, pharma R&D, GMP certification is a must.

• Languages: English, Good to have written & spoken French proficiency but it's not a Must.  

Pursue Progress, discover Extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

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