Lead design configuration and commissioning of DeltaV and PAS-X automation systems for GMP-critical manufacturing equipment and process controls.
Support change controls deviations and CAPAs involving DeltaV and PAS-X logic batch strategies and alarm configuration in collaboration with QA and Validation.
Develop and modify control modules phases and equipment modules within DeltaV in alignment with S88 batch architecture standards.
Provide hands-on troubleshooting and root cause analysis for DeltaV and PAS-X system issues during routine operations and project start-up phases.
Collaborate with cross-functional teams (Process Engineering QA Validation and Manufacturing) to align automation changes with business needs.
Author and review technical documentation including Functional Design Specs (FDS) software requirement specs and test protocols.
Interface with PAS-X MES and data historians to ensure integration and data continuity across digital systems.
Participate in system upgrades patching and security hardening activities to maintain compliance and cyber-resilience of DeltaV and PAS-X environments.
Train and mentor site engineers/operators on DeltaV and PAS-X operations change management and system maintenance best practices.
Ensure automation compliance
3 5 years of automation experience within pharmaceutical or biopharmaceutical manufacturing.
Experience with PAS-X and DeltaV highly preferred
Experience working within FDA remediation projects
Bachelors degree in Engineering or equivalent discipline.
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.