Transport-Jobs in Kanada

Ready to grow your skills while helping shape the future of healthcare? At Sanofi, you’ll be empowered to learn, ask questions, and bring your ideas to life – all while supported by inspiring mentors and collaborative teams.

Sanofi strategic direction is to standardize processes across sites, to embrace the digital transformation of its Manufacturing & Supply perimeter, looking at the opportunity to simplify its current solution landscape and leverage advanced technologies to bring business value.

In that context, the MARS program aims to implement the Computer-assisted batch review, enabled by the definition and roll-out of a core Manufacturing Execution System (MES). The MARS (MES Accelerated Roadmap @ Sanofi) program will transform Sanofi plants, improving compliance, cost and cycle time performance.

Over the last 3 years, Sanofi has deployed 30 Production sites across 4 GBUs (multiple and different pharmaceutical processes, 18 Weighing & Dispensing & 12 full MES), and a second wave, should start in the coming years (> 50 production sites, pending business case confirmation).

• Design standardized end-to‑end processes to generate business value and deliver best‑in‑class solutions to our industrial sites, with a high focus on electronic batch record management (content, execution) & review by exception process;
• Deliver innovative “state‑of‑the‑art” tools enabling performance for manufacturing processes across the Manufacturing & Supply sites;
• Allow new generation of deployment – more Agile & business centric
• Maintain robust and highly available solutions to operate industrial processes efficiently

The Manufacturing Execution System (MES) Product Configuration Lead drives the design, build and lifecycle of global end to end MES solutions (addition of interactive various components working together) as well as operational excellence to meet business needs in an operational and financially efficient manner. You guarantee and promote the right usage of Sanofi Digital and Industrial standards for Processes, Applications and Infrastructure environments. You leverage on Digital Portfolio the Detail Design document, catalogue of services and existing building blocks. You will work in close collaboration with MES Digital Product Owners, MES DevOps Engineers, MES developers, Product lines, Local digital & business teams, Business Process Owners and Archetype leads. You remain up to date on company’s standards, Digital industry practices and emerging standards and contributes to Digital standards maintenance.

• Master batch record edition & approval (including workflows)
• Master batch record review & approval (by Exception)
• Guidances / instructions
• Weighing & Dispensing
• Communication to equipements or scada systems
• Equipment management
• Material flow management
• Traceability / Genealogy
• Labelling
• Reporting
• Articulation with ERP, quality, logistic & shopfloor systems (LIMS, Documentation, Deviation management, Serialisation, OEE…)

We’re an R&D‑driven, AI‑powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

• Understand the business requirements (including analytics ones) for the various processes in their domain, be able to challenge, to consolidate and to extrapolate them in order to build solutions expendable to multi‑GBU use cases and plant configuration
• Provide functional & technical leadership during the full lifecycle and ensure adoption and adequate uses of the solution.
• Maximize customer satisfaction considering also to minimize build and maintenance costs, and risks associated with fulfillment of Business needs
• Propose innovative Digital solution to address new business needs creating competitive advantage
• Implement the appropriate services to ensure optimal allocation of all available capabilities

• Ensure functional lead & expertise to project teams across the MARS program & the sites
• Facilitate the transfer of know‑how, experience and best practices
• Contribute to Digital skills development within your domain

• Design and build core solutions as close to standard market solutions as possible, on the basis of state‑of‑the‑art best practices and aiming at aligning processes and enabling industrial efficiency across the different industrial sites of Sanofi.
• Contribute of the on‑time delivery of projects of domain ensuring robust, cost effective solutions while ensuring customer satisfaction, and business value focus
• Safeguard the proper deployment of core solutions on the different industrial sites
• Evaluate impact analysis on solution options and assesses and manages associated risks
• End‑to‑end business process analysis including integration with partner systems (ERP, other shopfloor systems, automation layers), labelling technologies, and mobile technologies
• Participate in the definition of indicators for performance and quality of service, monitor and communicate them
• Ensure the compliance of the solutions within the area in relation to legal and regulatory requirements

• Remain current on technology trends and Benchmark with other companies and partners to bring innovative inputs to our solutions, operating models and to our strategy
• Collaborate with peers (Enterprise Architects, other solution architects, Cybersecurity team, technical architects…) to review solution design and/or introduction of new technology to ensure compliance with Sanofi standards
• Explains / presents architecture and technical matters in an understanding way to Digital management team, staff and business stakeholders. Able to explain complex matters in a simple and understandable way
• Breaks current Gxp Validation established postulates to simplify and adapt to current and next generation technologies & methodologies (Cloud, Service Management, Agile), without Quality regression on documentations and validation processes

• 10+ years work experience in Manufacturing/Automation domain
• Demonstrated experience in a multicultural/multilanguage environment and in a matricial organization.
• Broad knowledge of Manufacturing Processes in industrial plants
• Significant MES experience: market standards knowledges (solutions, technologies, integration), process industry within life science / pharmaceutical industries
• Successful and significant Project Management experience would be a plus

• Expertise in MES solution Werum PAS‑X or Siemens OPCEnter Pharma execution
• Strong knowledge Manufacturing Execution System, including Master Batch Record and Review by Exception business processes and relevant MES solutions/modules/functionalities
• Strong Knowledge of pharma industry regulatory context (GxP)
• Strong communication, and interaction skills. Able to drive change management
• Knowledge of Solution architecture, infrastructure & integration (AWS, Azure, Windows / Oracle architectures, Middlewares, Cyber Security rules, low code platform as Mendix, mobility technologies…)
• Knowledge of Digital Development technologies (eg. C#, VBscript, HTML, CSS, Powershell, XML)
• Knowledge of Reporting tools (eg. Power BI, Crystal reports…)
• Ability to challenge, open minded and active listening
• Ability to collaborate and build effective network inside and outside Sanofi
• Ability to evaluate processes/solution to improve performance and drive continuous improvement
• Proven vision, ability to anticipate evolutions due to internal and external factors.

• Bachelors degree required in Engineering related field, or master in Computer Science or related field (or equivalent experience)

• 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

This position is for a current vacant role that we are actively hiring for.

Sanofi is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. We welcome and encourage applications from all qualified applicants. Accommodations for persons with disabilities required during the recruitment process are available upon request.

#GD-SP

#LI-SP

#LI-Hybrid

#DBBCA

All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

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.