OSD Manufacturing Expertise Automation Engineer

Job Summary

Horizon Controls Group is seeking an experienced Oral Solid Dosage (OSD) Manufacturing Expertise Automation Engineer to support the design integration optimisation and lifecycle management of automation systems within a highly advanced pharmaceutical manufacturing environment.

This role requires a strong combination of automation engineering capability and deep manufacturing process expertise within Oral Solid Dosage operations. The successful candidate will provide technical leadership across OSD process automation supporting both capital projects and operational manufacturing systems while ensuring compliance with GMP data integrity and Lilly engineering standards.

The position will focus heavily on automation. Solutions supporting tablet manufacturing coating technologies spray drying operations and integration of critical utility systems including CIP purified water systems and process tanks.

Key Responsibilities

• Provide automation engineering expertise for Oral Solid Dosage manufacturing processes across production and project environments.
  
• Lead the design development configuration and optimisation of automation systems supporting OSD manufacturing equipment and utilities.
  
• Support automation strategies for tablet presses coating systems spray drying technologies and associated material handling processes.
  
• Develop and maintain PLC HMI batch and process control logic to ensure safe compliant and efficient manufacturing operations.
  
• Collaborate closely with manufacturing process engineering CQV quality maintenance and digital teams to support production readiness and process optimisation.
  
• Support integration of manufacturing equipment with utilities and site-wide automation infrastructure including CIP systems purified water systems tanks and process utilities.
  
• Participate in automation architecture reviews process hazard assessments FAT/SAT execution commissioning qualification and startup activities.
  
• Troubleshoot complex automation and process control issues within live manufacturing operations.
  
• Support data integration historian systems MES interfaces and manufacturing reporting solutions where applicable.
  
• Develop and review technical documentation including functional specifications control narratives IO lists test protocols and change controls.
  
• Ensure all automation activities comply with GMP GAMP5 ISA-88 ISA-95 cybersecurity and data integrity requirements.
  
• Contribute to continuous improvement initiatives focused on process efficiency reliability and operational excellence.
  

Required Technical Expertise

OSD Manufacturing Process Knowledge

The successful candidate must demonstrate strong hands-on understanding and automation support experience within the following process areas:

• Tablet Presses and Coating Systems
  Experience supporting automated tablet compression equipment coating systems recipe management batch sequencing and process optimisation within OSD manufacturing environments.
• Spray Drying Processes
  Strong process and automation understanding of spray drying operations including process control strategies temperature and airflow control material handling and process monitoring. This is considered a key requirement for the role.
• Utilities Integration
  Experience integrating manufacturing systems with process utilities including CIP systems purified water systems process tanks skids and associated utility automation infrastructure.

Requirements

Required Experience & Qualifications

• Degree in Automation Electrical Chemical Process Pharmaceutical or related Engineering discipline.
  
• Significant automation engineering experience within pharmaceutical or regulated manufacturing environments.
  
• Strong expertise supporting OSD manufacturing processes and associated process equipment.
  
• Hands-on experience with PLC SCADA HMI batch control systems and industrial automation platforms.
  
• Proven capability in automation system design troubleshooting commissioning and operational support.
  
• Strong understanding of GMP GAMP5 ISA-88 ISA-95 and pharmaceutical validation requirements.
  
• Experience supporting commissioning FAT/SAT IQ/OQ and startup activities.
  
• Ability to work effectively across multidisciplinary projects and operational teams.
  
• Strong analytical troubleshooting and problem-solving skills.
  

Preferred Experience

• Experience supporting large-scale pharmaceutical manufacturing projects.
  
• Exposure to MES systems historian platforms or digital manufacturing initiatives.
  
• Experience within continuous manufacturing or advanced process control environments.
  
• Familiarity with data analytics process optimisation or Industry 4.0 technologies.
  
• Previous experience in greenfield pharmaceutical facility projects.
  

Key Competencies

• Deep OSD manufacturing process expertise
  
• Strong automation and controls engineering capability
  
• Technical leadership and stakeholder collaboration
  
• High attention to quality and compliance
  
• Strong troubleshooting and root cause analysis skills
  
• Continuous improvement and innovation mindset