Sanofi, a leading global biopharmaceutical company, is seeking a Master Batch Record (MBR) Developer to join their digital transformation initiative. This role is part of the MARS (MES Accelerated Roadmap @ Sanofi) program, which aims to implement Computer-assisted batch review through a core Manufacturing Execution System (MES).
The position involves working with Siemens OPCenter Execution Pharma and Equipment logbook systems, requiring expertise in manufacturing execution systems and pharmaceutical processes. The ideal candidate will have 3-5 years of relevant experience and a strong technical background in computer science.
As an MBR Developer, you'll be responsible for building, testing, and implementing Master Batch Records within the MES environment. You'll work closely with various teams including MES Digital Product Configuration experts, Product lines, and local digital teams to ensure successful implementation across Sanofi manufacturing sites.
The role combines technical expertise with business process understanding, covering areas such as master data management, production execution, weighing & dispensing, and integration with various systems. You'll need to ensure all configurations meet GMP requirements and data integrity standards while following established methodologies for GxP validations.
This is an excellent opportunity for someone passionate about healthcare technology and manufacturing processes, offering exposure to cutting-edge manufacturing execution systems and the chance to work in a global, matrix organization. The position requires occasional travel to manufacturing sites and the ability to work across different time zones and cultures.
Sanofi offers a collaborative environment focused on innovation and transformation in healthcare manufacturing. They value diversity and inclusion, providing equal opportunities to all employees regardless of background. The company's commitment to standardizing processes and embracing digital transformation makes this an exciting role for someone looking to make a significant impact in pharmaceutical manufacturing technology.