Job Description
About PSC Biotech
Who are we?
PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients.
‘Take your Career to a new Level’
PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling point which includes the opportunity to work with the most talented cohort of like-minded professionals operating in the Pharma / Biotech Industry. We offer a permanent contract of employment giving exposure of working in Top Pharmaceutical client sites in a diverse-cultural work setting.
Employee Value Proposition
Employees are the “heartbeat” of PSC Biotech, we provide unparalleled empowering career development though Learning & Development in-house training mentorship through constant guidance to facilitate career progression. We believe in creating high performing teams that can exceed our client’s expectations with regards to quality of all scalable and business unit deliverables, staying under budget and ensuring timelines for our deliverables are being met.
Overview :
Hybrid Role : 3 days on site (Tuesday, Wednesday and Thursday) mandatory required
Requirements
Role Functions :
System Coordination : Serve as the primary technical point of contact for all DeltaV DCS-related projects and operations within pharmaceutical manufacturing facilities.
Implementation & Validation : Lead the implementation, configuration, and validation of DeltaV systems in accordance with FDA regulations, 21 CFR Part 11, and GMP guidelines.
Configuration & Programming : Develop, configure, and test DeltaV control strategies, logic, and operator interfaces to meet pharmaceutical process requirements.
Troubleshooting & Support : Provide expert troubleshooting and root cause analysis for DeltaV system issues, ensuring minimal downtime and compliance with quality standards.
Documentation & Compliance : Maintain detailed documentation including system design specifications, validation protocols (IQ / OQ / PQ), change control records, and SOPs to support audits and regulatory inspections.
Training : Train operators, engineers, and maintenance personnel on DeltaV system operation, change management, and compliance requirements.
Vendor & Audit Coordination : Collaborate with Emerson, system integrators, and quality assurance teams during audits, inspections, and vendor assessments.
Continuous Improvement : Identify and implement system enhancements to improve process control, data integrity, and operational efficiency while maintaining compliance.
Risk Management : Participate in risk assessments and mitigation planning related to control system changes and upgrades.
Knowledge, Skills, Education & Location Requirements :
Requirements
The Delta V Technical Coordinator is responsible for managing and coordinating all technical activities related to the Emerson DeltaV Distributed Control System (DCS) Hardware and Software delivery to ensure compliant, reliable, and efficient automation of pharmaceutical API manufacturing processes. Familiarity with Agile Ways of working and support the implementation of the DeltaV Software Delivery through Agile methodology.
Automation • Tipperary, TA, ie