Production Support- Vaccines

About the Job

We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. Your job, as Professional Production Support within our Recombinant Drug Substance Manufacturing Facility, will contributes as a member of Manufacturing & Supply - Building 55 Recombinant Drug Substance Manufacturing Facility and functions as a primary interface with the Technical Community, especially ITS, Automation & Manufacturing Excellence for Digital solutions such as MES, DCS & ERP systems.

We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.​

Main Responsibilities:

• Accountable for ensuring production needs and user requirements are satisfied in ITS, Automation and Digital solutions and platforms, such as MES- eBatch Records & eLogbooks, the facility’s Process Control System, ERP systems, etc. 

• Act as a production representative for the facility with an emphasis and focus on digital, automation and ITS related platforms.

• Act as a point of contact for production with MES & Automation system integration experts.  Ensure communications from production shop floor team are properly understood by system integrators.

• Understand & employ computer programming and scripting to solve problems and integrate existing tools to achieve continuous improvement and perform minor edits to existing eBRs and eLogbooks.

• Support the development of production recipes, bill of materials in SAP and Process Control System.

• Responsible for accuracy of master batch record & process instruction content specific to the manufacturing process to support MES. Performs & supports the coordination of reviews and approvals of MES & Automation documentation such as but not limited to: User Acceptance Testing (UAT), Process Instructions, Functional Specifications.

• Supports UAT executions with coordination, defect resolution 

• Participate in general production activities, commissioning, qualification, and validation activities, event investigations and other assignments to support the manufacturing team.

• Support adherence to schedule with task ownership, meeting task durations

About You

Basic Qualifications:

• Bachelor of Science (Computer Engineering, Cybersecurity, Computer Programming)

• At least 1 year of relevant experience (MES/automation)

Other Skills:

• MES Development experience, especially with Siemens Opcenter.

• Must have excellent communication skills as well as the ability to work with cross functional teams, cooperate transversally, demonstrated the ability to strive for results.

Why Choose Us?

• Bring the miracles of science to life alongside a supportive, future-focused team.

• Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.

• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.

• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.

​Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

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