The Growth Automation Engineer role is designed for early-career engineers who are eager to develop expertise in industrial automation within a GMP-regulated pharmaceutical environment. This position offers hands-on experience with control systems manufacturing technologies and digital systems that support production operations.
The successful candidate will work closely with senior automation engineers operations and IT teams to support automation systems troubleshoot issues and contribute to continuous improvement and digitalisation initiatives across the site.
Key Responsibilities
Automation & Technical Support
Provide day-to-day support for automation and control systems used in manufacturing and utilities.
Assist in troubleshooting issues related to PLC SCADA and DCS systems to minimise downtime.
Support maintenance and reliability of automation systems and associated hardware.
Monitor system performance and escalate issues where necessary.
Control Systems & Technologies
Gain hands-on experience with automation platforms such as:
Support system configuration testing and modifications under supervision.
Assist in maintaining system documentation backups and version control.
Project & Continuous Improvement
Support automation-related projects including system upgrades and new implementations.
Contribute to process optimisation and digital transformation initiatives.
Participate in root cause analysis (RCA) and implement corrective actions.
Assist in the development and execution of small automation improvement projects.
Validation & Compliance
Operate in compliance with GMP EHS and site quality standards.
Support validation activities including IQ OQ and PQ for automation systems.
Assist in preparing and reviewing validation and technical documentation.
Ensure adherence to data integrity and cybersecurity standards.
Collaboration & Stakeholder Engagement
Work closely with Manufacturing Quality Maintenance and IT teams.
Support cross-functional problem-solving and continuous improvement initiatives.
Communicate effectively with team members and escalate issues appropriately.
Learning & Development
Participate in structured training programs focused on automation systems and GMP compliance.
Develop technical competencies in control systems programming and troubleshooting.
Build knowledge of pharmaceutical manufacturing processes and regulatory requirements.
Requirements
Education
Experience
Technical Skills
Basic understanding of automation and control systems (PLC SCADA DCS)
Exposure to programming environments (e.g. Siemens TIA Portal Studio 5000) is desirable
Familiarity with IT systems networks and data systems is an advantage
Proficiency in Microsoft Office and basic data analysis
Regulatory & Industry Knowledge (Desirable)
Understanding of GMP (Good Manufacturing Practice)
Awareness of validation principles (IQ/OQ/PQ)
Knowledge of data integrity and regulatory requirements in pharma
Key Competencies
Strong willingness to learn and develop technical skills
Analytical thinking and problem-solving ability
Good communication and teamwork skills
Attention to detail and compliance mindset
Ability to work in a fast-paced regulated environment
The Growth Automation Engineer role is designed for early-career engineers who are eager to develop expertise in industrial automation within a GMP-regulated pharmaceutical environment. This position offers hands-on experience with control systems manufacturing technologies and digital systems that ...
The Growth Automation Engineer role is designed for early-career engineers who are eager to develop expertise in industrial automation within a GMP-regulated pharmaceutical environment. This position offers hands-on experience with control systems manufacturing technologies and digital systems that support production operations.
The successful candidate will work closely with senior automation engineers operations and IT teams to support automation systems troubleshoot issues and contribute to continuous improvement and digitalisation initiatives across the site.
Key Responsibilities
Automation & Technical Support
Provide day-to-day support for automation and control systems used in manufacturing and utilities.
Assist in troubleshooting issues related to PLC SCADA and DCS systems to minimise downtime.
Support maintenance and reliability of automation systems and associated hardware.
Monitor system performance and escalate issues where necessary.
Control Systems & Technologies
Gain hands-on experience with automation platforms such as:
Support system configuration testing and modifications under supervision.
Assist in maintaining system documentation backups and version control.
Project & Continuous Improvement
Support automation-related projects including system upgrades and new implementations.
Contribute to process optimisation and digital transformation initiatives.
Participate in root cause analysis (RCA) and implement corrective actions.
Assist in the development and execution of small automation improvement projects.
Validation & Compliance
Operate in compliance with GMP EHS and site quality standards.
Support validation activities including IQ OQ and PQ for automation systems.
Assist in preparing and reviewing validation and technical documentation.
Ensure adherence to data integrity and cybersecurity standards.
Collaboration & Stakeholder Engagement
Work closely with Manufacturing Quality Maintenance and IT teams.
Support cross-functional problem-solving and continuous improvement initiatives.
Communicate effectively with team members and escalate issues appropriately.
Learning & Development
Participate in structured training programs focused on automation systems and GMP compliance.
Develop technical competencies in control systems programming and troubleshooting.
Build knowledge of pharmaceutical manufacturing processes and regulatory requirements.
Requirements
Education
Experience
Technical Skills
Basic understanding of automation and control systems (PLC SCADA DCS)
Exposure to programming environments (e.g. Siemens TIA Portal Studio 5000) is desirable
Familiarity with IT systems networks and data systems is an advantage
Proficiency in Microsoft Office and basic data analysis
Regulatory & Industry Knowledge (Desirable)
Understanding of GMP (Good Manufacturing Practice)
Awareness of validation principles (IQ/OQ/PQ)
Knowledge of data integrity and regulatory requirements in pharma
Key Competencies
Strong willingness to learn and develop technical skills
Analytical thinking and problem-solving ability
Good communication and teamwork skills
Attention to detail and compliance mindset
Ability to work in a fast-paced regulated environment
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