OSD Manufacturing Expertise Automation Engineer
Description
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
