Manufacturing and Supply
Where the
miracles of
science are made
a reality for patients

JOB PURPOSE

Reporting directly to the Supply Chain Master Data Head, he/she is assigned, to the Master Data processes and associated Workflows, related to clients and Third Parties, Raw Materials, Consumables, Packaging Supplies, and Logistics Services required for their activity, at the lowest cost of implementation in the short, in conformity with the defined quality, technical and logistical specifications, Marking Plans, GOP/SOP, within deadlines and planning, adherent to Quality & HSE policies, Sanofi's procedures, ethical rules and values.

JOB RESPONSABILITIES

• Comply with the standards (external or internal) regarding labor legislation, quality protocols, respect for the environment and safety at work.

• Apply the protocols established by HSE for the development of the functions of your job, Use of PPE, knowledge of documentation on the prevention of occupational hazards, legal authorizations for safe work and any other that may be applicable.

• Comply with the Quality regulations that apply to the development of its functions.

• Plans and structures the deployment of information under his/her responsibility related to the Rock Project.

• Entering Master Data in a Format or a workflow tool which is structured by the Data Stewards. He/she respects theses workflows structure & associated business rules.

• The Master Data Technician Support act as support of the Artwork Team.

• The Master Data Technician Support creation/modification GOP/SOP

QUALIFICATIONS AND KNOW-HOW

• Background in Supply Chain preferably in the pharmaceutical industry.

• Knowledge with planning & ERP systems, with the ability to derive recommendation out of provided data.

• Ability to engage and collaborate with multiple partners within site and global functions.

• Interpersonal skills: ability to engage and collaborate with multiple partners within site functions to gather information and assess feasibility. Proactivity is a must, given the anticipation component of the position. 

• Fluent in Spanish & English.

• Knowledge of GMP Compliance & Pharmaceutical regulations understanding

Note for candidates:

The Riells site, currently owned by Sanofi, is part of this transactional agreement and is planned to be transferred to Adamed. Candidates hired during this period will initially join with a Sanofi employment contract and will then be transferred to Adamed once the transaction is completed. 

By applying to this role your personal data will be processed solely for the purpose of assessing your application.  Your personal data will be managed jointly by the two participating companies Adamed and Sanofi, both of which will handle your information securely and in full compliance with GDPR, and retained only for the time necessary to complete the selection process.

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Pursue Progress. Discover Extraordinary.

Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.

Watch 'One day at Sanofi' and check out our Diversity Equity and Inclusion initiatives at sanofi.com