Join Capgemini and drive digital transformation in manufacturing with a focus on smart factory solutions and Industry 4.0. This role is crucial for enhancing operational excellence, compliance, and performance within Life Sciences and Medical Devices.

We are seeking a seasoned MES Consultant specializing in Siemens Camstar or Critical Manufacturing. You will be instrumental in implementing, integrating, validating, and optimizing MES solutions in regulated environments. Collaboration with stakeholders is key to delivering compliant and scalable manufacturing systems.

Lead MES implementation, enhancement, and support projects using Siemens Camstar and/or Critical Manufacturing MES platforms.

Translate business needs into detailed functional and technical MES solutions, configuring capabilities like Electronic Batch Records (EBR), Weigh & Dispense, Genealogy, and Quality Management.

Facilitate seamless integration of MES with ERP, LIMS, SCADA, automation, and serialization systems.

Ensure compliance through Computer System Validation (CSV) activities adhering to GxP, GMP, FDA 21 CFR Part 11, and GAMP5 guidelines.

Drive testing, deployment, go-live support, and continuous improvement initiatives while collaborating across manufacturing, quality, validation, engineering, and IT teams.

A minimum of 10 years of experience in MES, Manufacturing IT, or Digital Manufacturing is required.

Demonstrated hands-on experience with Siemens Camstar and/or Critical Manufacturing MES is essential.

Possess a strong understanding of manufacturing processes within Life Sciences, Pharmaceutical, Biotechnology, or Medical Devices.

Familiarity with MES integrations, SQL, APIs, manufacturing data management, ISA-95 standards, and Industry 4.0 concepts is expected.

Excellent analytical, communication, problem-solving, and stakeholder management skills are crucial for success in this role.