Roles & Responsibilities:
- Lead design configuration and commissioning of DeltaV and Client-X automation systems for GMP-critical manufacturing equipment and process controls.
- Support change controls deviations and CAPAs involving DeltaV and Client-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 Client-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 Client-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 Client-X environments.
- Train and mentor site engineers/operators on Delta and Client-X operations change management and system maintenance best practices.
- Ensure automation compliance
- 35 years of automation experience within pharmaceutical or biopharmaceutical manufacturing.
- Experience with Client-X and Delta highly preferred
- Experience working within FDA remediation projects
- Bachelors degree in engineering or equivalent discipline.
Additional Information :
All your information will be kept confidential according to EEO guidelines.
Remote Work :
No
Employment Type :
Contract