Looking to speak with Automation professionals with strong experience inManufacturing Control Systems, OT, Machine Automation, and Digitalizationfor a leading pharmaceutical manufacturing site.Key ResponsibilitiesAct as SME and system administrator for site automation systems.Monitor and optimize computerized system performance to ensure maximum uptime.Manage system access, backups/restores, patching, and troubleshooting (including vendor escalation).Lead or participate in investigations related to control system deviations.Identify and deliver small automation improvement projects.Support site Automation & Digitalization initiatives, including:Participating in capital planning and project teamsInstalling/configuring hardware/softwareCreating system documentation (URS, FDS, network architectures, SOPs)Developing test scripts and qualification protocolsContributing to automation lifecycle and roadmapsDevelop and implement automation strategies aligned with global best practices.Support lifecycle management of production systems, equipment, and infrastructure.Ensure all automation solutions meet site needs, compliance requirements, and quality standards.Lead site working groups and drive automation rollouts to meet cost, schedule, and technical objectives.Maintain data integrity and documentation accuracy across all systems.Technical ExpertiseCandidates should have strong experience with:PLC/HMI/SCADA technologies (Siemens, Omron, Mitsubishi, iFix, Wonderware, Inmation).Industrial protocols (OPC, Modbus, Ethernet/IP, Profinet, Profibus).SQL databases, scripting, and data management tools.GAMP lifecycle, 21 CFR Part 11, Annex 11, ISA-88/95/101/105/106.Network architecture: TCP/IP, routing, switching, IDS/IPS, Active Directory, firewalls.Strong analytical, troubleshooting, and documentation skills.Solid understanding of pharmaceutical manufacturing and regulatory environments.Collaboration & Stakeholder EngagementStrong communicator and team player with the ability to influence and collaborate across functions.Comfortable engaging internal/external stakeholders and supporting cross-site standardization.Ability to mentor and upskill colleagues in automation best practices.Independent, organised, and adaptable within a fast-paced GMP manufacturing environment.RequirementsDegree in Engineering (Automation, Robotics, Computer Science, Electrical, Mechanical, Chemical, or similar).Minimum 5 years' experience in GMP manufacturing with solid automation expertise.Strong understanding of data integrity, documentation best practice, and GxP/QA requirements.Experience managing external vendors and service contracts.Excellent analytical, communication, and problem-solving abilities.Desirable SkillsExperience with data analytics.Familiarity with ANSI/ISA-99/100.Broad understanding of the pharmaceutical industry beyond technical aspects.