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Support retirement of DeltaV automation and computerized control systems.
Prepare impact assessments, change controls, and validation closeout documentation.
Support D3 decommissioning activities alongside technical engineering resources.
Coordinate with Engineering, Automation, Validation, and Quality teams to complete activities in compliance with GMP requirements.
Qualifications10+ years of pharmaceutical CSV, automation validation, or related U.S. experience.
Must have hands-on experience with Emerson DeltaV systems.
Must have experience authoring and executing GMP validation protocols and documentation.
Strong understanding of computerized system lifecycle, change control, and GMP requirements.
Must have the ability to independently manage validation documentation and execution.
Must have previous automation or computerized system decommissioning experience.
Experience with D3 systems or related documentation.
Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.
Now viewing: CSV Validation Engineer (DeltaV)
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Sterling Engineering, Inc.
CSV Validation Engineer (DeltaV)
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Job Description
Position:
CSV Validation Engineer (DeltaV)Duration:
18-24 monthsLocation:
Waukegan, IL 60087 - 100% onsite, 5 days per week Join our Sterling Engineering team! Sterling Engineering is seeking an experienced DeltaV / CSV Validation Engineer to support the GMP-compliant retirement of pharmaceutical automation and computerized control systems. This role focuses on developing and executing validation and decommissioning documentation. Candidates should bring hands-on Emerson DeltaV experience and the ability to independently manage GMP documentation and execution. ResponsibilitiesDevelop and execute decommissioning plans, protocols, and validation documentation.Support retirement of DeltaV automation and computerized control systems.
Prepare impact assessments, change controls, and validation closeout documentation.
Support D3 decommissioning activities alongside technical engineering resources.
Coordinate with Engineering, Automation, Validation, and Quality teams to complete activities in compliance with GMP requirements.
Qualifications10+ years of pharmaceutical CSV, automation validation, or related U.S. experience.
Must have hands-on experience with Emerson DeltaV systems.
Must have experience authoring and executing GMP validation protocols and documentation.
Strong understanding of computerized system lifecycle, change control, and GMP requirements.
Must have the ability to independently manage validation documentation and execution.
Must have previous automation or computerized system decommissioning experience.
Experience with D3 systems or related documentation.
Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.
Benefits
- Dental Insurance