United Consulting Hub is seeking a Junior Automation Engineer to support the design, implementation, and maintenance of automation systems within pharmaceutical or medical device manufacturing environments. The role involves working with control systems and ensuring compliance with regulatory standards such as GMP and FDA requirements.
Responsibilities:
- Assist in the design, development, and implementation of automation systems and control strategies
- Support PLC, HMI, and SCADA system configuration and troubleshooting
- Assist in programming and modifying control systems (e.g., Siemens, Allen-Bradley, DeltaV)
- Support commissioning and qualification (IQ/OQ/PQ) of automated equipment and systems
- Troubleshoot automation and process control issues in manufacturing environments
- Collaborate with cross-functional teams including Engineering, QA, Validation, and Operations
- Assist in preparing technical documentation, SOPs, and validation protocols
- Support data collection, analysis, and reporting for process improvements
- Ensure compliance with GMP, FDA, and regulatory requirements
- Participate in FAT (Factory Acceptance Testing) and SAT (Site Acceptance Testing) activities
- Assist in integrating automation systems with MES, historians, or other plant systems
- Support preventive maintenance and system upgrades
Requirements:
- Basic understanding of PLC, SCADA, and industrial automation systems
- Knowledge of control systems and instrumentation fundamentals
- Familiarity with automation platforms such as Siemens, Allen-Bradley, or DeltaV
- Understanding of GMP and regulated environments
- Basic programming knowledge (ladder logic, function blocks, or scripting)
- Strong analytical and troubleshooting skills
- Good communication and teamwork abilities
- 0–2 years of experience in automation, controls engineering, or related field
- Fresh graduates with relevant academic projects or internships are encouraged to apply
- Internship or project experience in the pharmaceutical, biotech, or medical device industry
- Exposure to validation (IQ/OQ/PQ) and documentation practices
- Familiarity with MES systems, data historians (OSI-PI), or industrial networks
- Knowledge of industry standards such as FDA, GAMP 5, or ISO guidelines
- Experience with AutoCAD or electrical drawings