This company is dedicated to pushing the boundaries of science and technology to create a healthier world. As a global leader in biopharmaceutical manufacturing, they prioritise innovation, quality, and efficiency in all aspects of their operations. Key responsibilities: Design, configure, and maintain Emerson DeltaV DCS in a GMP-regulated manufacturing environment. Develop and implement control strategies, batch configurations, and automation solutions to optimize system performance. Troubleshoot and resolve hardware and software issues to ensure minimal downtime. Collaborate with cross-functional teams including process engineers, validation specialists, and quality assurance teams to support production goals. Support system validation, commissioning, and qualification activities to ensure compliance with FDA, GMP, and industry standards. Develop and update technical documentation, including functional specifications, design documents, and standard operating procedures (SOPs). Provide training and technical support to end users and other engineering personnel. Stay updated with industry trends, best practices, and emerging technologies in automation and process control. Qualifications and Experience: Bachelor’s degree in Electrical Engineering, Chemical Engineering, Computer Science, or a related field. 3+ years of experience working with Emerson DeltaV DCS in a pharmaceutical, biotechnology, or manufacturing environment. Strong understanding of GMP regulations, FDA guidelines, and validation processes. Proficiency in automation protocols, batch processing, and control system design. Experience with scripting and database management (SQL, VBA, Python) is a plus.