Type : ContractLocation :Algete, Community of Madrid, Spain-2/3 days a week onsite
Responsibilities:
Work closely with Site team responsible for manufacturing equipment to provide technical guidance and support in the integration of equipment for Manufacturing Execution System (MES).Responsible for the MES integration pack, roadmap and deliverables. Liaise with site engineering leads and automation engineers.Strong experience with MES & Automation systems.Facilitating and continuing regular Agile planning for MES integrationAnalysis and solving technical issues related to the MES integration.Manage activities of URS/FRS generation, software configuration/coding and general oversight to the MES software documentation practicesA thorough understanding of system cGMP requirements and demonstrable knowledge of computer system design and maintenance lifecycle in cGMP environments.Liaise where necessary with MES platform provider, engineering contractor, and equipment vendors on the lifecycle of document preparation, approval, coding, and delivery
Essential skills/knowledge/experience:10+ years’ experience in MES integrationMES (Rockwell FTPS) Development & Customization: Proficient in configuring and extending pharma MES platforms to support GMP-compliant manufacturing processes.System Integration: Skilled in integrating MES with ERP, LIMS, SCADA, and shop-floor equipment using APIs, OPC UA, and middleware tools.SQL & Scripting Expertise: Strong in SQL, stored procedures, and scripting (e.G., Python, JavaScript) for data handling, reporting, and workflow automation.Process Knowledge: Deep understanding of pharma manufacturing workflows including batch execution, weigh & dispense, and electronic batch records (EBR).