DELTAV BATCH ENGINEER

• Design and implement process automation systems and solutions to manage a batch pharmaceutical manufacturing environment • Hands on experience performing DeltaV Batch configuration • Manage software development projects from design to implementation for new automation configuration/data collection systems and expansion to existing systems • Support in system FAT and SAT • Support troubleshooting and investigation of production process, equipment, systems and code/configuration related to quality or safety issues. Implement the relevant improvement solutions • On-Call support for Biologics Manufacturing and API plants, • Improvements/troubleshooting of existent Control Strategies, • Project progressing according to plan and quality expectations • Commissioning and qualification activities for new logic implementation • Develop Functional Specifications (FS) and Design Specifications (DS) in alignment with Client’s site requirements. • Review PCS-related design documentation and provide feedback to ensure compliance with user requirements and approved standards. • Track project deliverables, maintain documentation, and ensure adherence to the agreed schedule. • Batch software commissioning and functional testing • Qualification testing, including Installation Qualification (IQ) and Operational Qualification (OQ) • Support Engineering and Performance Process Qualification (PPQ) batches as required. • Support and track change management processes throughout the project lifecycle. Requirements • Min. 3 years experience in DeltaV System, DeltaV Batch Software Design and Configuration. • Degree in Chemical/Electrical Engineering, Computing or IT • Excellent problem-solving ability and customer-focused • Strong technical writing and documentation skills are required • Must be proactive, have experience with high performance teams • Good teamwork and communication skills; ability to interact across functional teams at multiple levels within the organization • Good skills in Windows operating system administration, programmable logic controllers, Visual Basic programming, databases and general programming would be added advantage • Technical knowledge and experience with validation/qualification of pharmaceutical processes, equipment, utilities, facilities and/or computer systems. • Have trouble shooting capabilities. Be able to use engineering thinking and principles to tackle complex technical/process issues. • Have working knowledge of FDA Regulations/Guidance, and Good Manufacturing Practices • Skills: Process Automation, System Administration, Test Strategy, Troubleshooting, Virtualisation, Control Systems, Databases, DCS, Documentation Skills, FDA, Liaising with cross functional teams, Management Skills, Manufacturing, on-call support, Pharmaceutical Manufacturing, Project Management, Software Design, Software Development, Technical Writing, Windows