We are seeking an experienced MES Integration Lead to support the integration of manufacturing equipment with our Manufacturing Execution System (MES) in a highly regulated pharmaceutical environment.This role will work closely with site engineering, automation, and manufacturing teams to deliver robust, GMP-compliant MES solutions that support digital manufacturing and electronic batch record initiatives.Key Responsibilities
La siguiente información ofrece un resumen de las habilidades, cualidades y cualificaciones necesarias para este puesto.
Provide technical leadership and guidance for the integration of manufacturing equipment with the MES platform.Own and manage the MES integration roadmap, integration pack, and key deliverables.Collaborate with site engineering leads, automation engineers, and manufacturing teams to ensure successful MES deployment.Facilitate and drive Agile planning and delivery for MES integration projects.Analyse and resolve technical issues related to MES integration and system performance.Lead the creation and management of URS, FRS, and MES software documentation.Oversee software configuration, coding activities, and MES documentation practices.Ensure compliance with c GMP regulations and validated computer system lifecycle requirements.Coordinate with MES platform providers, engineering contractors, and equipment vendors across the project lifecycle. Required Skills & Experience
10+ years' experience in MES integration, ideally within pharmaceutical or life sciences manufacturing.Strong experience with MES platforms, particularly Rockwell Factory Talk Pharma Suite (FTPS).Proven ability to configure, customise, and extend MES platforms for GMP-compliant manufacturing processes.Experience integrating MES with ERP, LIMS, SCADA, and shop-floor equipment.Strong knowledge of industrial communication technologies such as APIs, OPC UA, and middleware solutions.Advanced SQL expertise, including stored procedures and database management.Experience with scripting languages such as Python or Java Script for automation and reporting. xcskxlj Deep understanding of pharmaceutical manufacturing workflows, including:Electronic Batch Records (EBR)Weigh & DispenseBatch execution processesStrong knowledge of c GMP requirements and validated computer system lifecycle practices. What We're Looking For
A proactive technical leader with strong collaboration skillsExperience working in cross-functional engineering and IT teamsPassion for digital manufacturing and Industry 4.0 transformation If you're an experienced MES professional looking to lead complex integration projects in a regulated manufacturing environment, we'd love to hear from you.