Looking to speak with Automation professionals with strong experience in
Manufacturing Control Systems, OT, Machine Automation, and Digitalization
for a leading pharmaceutical manufacturing site.
Key Responsibilities
* Act 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 teams
* Installing/configuring hardware/software
* Creating system documentation (URS, FDS, network architectures, SOPs)
* Developing test scripts and qualification protocols
* Contributing to automation lifecycle and roadmaps
* Develop 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 Expertise
Candidates 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 Engagement
* Strong 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.
Requirements
* Degree 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 Skills
* Experience with data analytics.
* Familiarity with ANSI/ISA-99/100.
* Broad understanding of the pharmaceutical industry beyond technical aspects.