Le contenu du poste est libellé en anglais car il nécessite de nombreuses interactions avec nos filiales à l’international, l'anglais étant la langue de travail.
This role is accountable for rigorous and efficient transfer and implementation of cell culture across the Sanofi GMP manufacturing network according to the program timelines.
The role of the BioProcess Engineering (BPE) group is to serve as a general lead for clinical transfers and sending lead for commercial transfers.
Responsibilities include but are not limited to partner with all relevant functions from R&D and IA to perform facility fit assessment and authorize transfer documents, specifically
Lead technical transfer activities including facility-fit assessment and operational readiness assessment and provide technical support as SME for cell culture processes
Support GMP manufacturing operations
Serve as People-In Plant (PIP) for critical steps during manufacturing campaigns
Organize regular review meetings during GMP campaigns with updates on process performance and deviations
Act as technical leader for deviations and CAPA definition to resolve complex process anomalies
Lead authorization of technology transfer plans, technology transfer reports, and campaign summary reports
Partner of risk assessment and control strategy definition by providing information and data on facility and equipment capability and constraints
Act as a data steward by gathering and compiling process data for projects with the support of all involved functions (Development, GMP manufacturing, and Analytics) for development runs, scale-up batches at technical pilot plant, and GMP batches at GMP manufacturing including process performance attributes and analytical results.
Visualization for reviews, assessments, and process anomaly root cause analysis
Lead evaluation and implementation of new process platforms and manufacturing technologies
As a senior member of the BPE group, work collaboratively with members of other functions to streamline the interfaces with various partners and represent the function in stakeholder meetings as needed
Along with BPE members at other sites, maintain and update the knowledge base of equipment and operation specifications across the entire Sanofi manufacturing network.
Share best practices in tech transfer and implementation and drive continuously improvement
Bachelors or Master's degree in Chemical Engineering, Biochemistry, Biotechnology, or related field with minimum of 12 years industrial experience in manufacturing or process development of biologics
Experience in leading matrix teams
Excellent oral and written communication skills to build relationships both inside and outside the company
Experience working on multiple complex projects to aggressive timelines with the ability to adapt to rapid changes in project priorities
Experience in manufacturing or process development of biologics, preferred produced in mammalian cell culture systems, with knowledge on scale-up, process transfer, and cGMP manufacturing operation
Experience in writing and revising protocols, procedures, reports and other process related documentation as necessary to support process scale-up, transfer, and implementation to cGMP manufacturing operations
Working knowledge in recombinant protein GMP manufacturing, quality standards, and regulatory requirements
Experience in defining process control strategy and process validation and performing risk assessment following the QbD principle
At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers.
We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.
As part of its diversity commitment, Sanofi is welcoming and integrating people with disabilities.