Global Compliance Partners
We are seeking an experienced
DeltaV Automation Engineer
to support commissioning, qualification, and validation (CQV) activities for a client in the Greater Seattle area. The ideal candidate will have hands‑on experience with Emerson DeltaV systems in GMP manufacturing environments and a solid understanding of automation life cycle documentation, validation principles, and GMP compliance.
Key Responsibilities
Support the
design, configuration, and commissioning
of DeltaV automation systems, including batch recipes, equipment modules, control strategies, and interfaces.
Develop and execute
validation protocols
(IQ/OQ/PQ) for automation systems in alignment with project timelines and regulatory requirements.
Author and review
URS, FRS, DS, CS, and testing documentation
following GAMP 5 guidelines.
Work with cross‑functional teams (Process, CQV, QA, MSAT) to ensure seamless integration of automation systems into the manufacturing process.
Provide
technical support
during system start‑up, qualification, and routine operations.
Support
change control, deviation, and CAPA
resolution related to automation and control systems.
Ensure all automation activities adhere to
21 CFR Part 11, Annex 11, and data integrity
requirements.
Qualifications
Bachelor’s degree in Engineering (Chemical, Electrical, or Automation) or related field.
5+ years of experience with
Emerson DeltaV
configuration and troubleshooting in GMP pharmaceutical or biotech environments.
Proven experience supporting
validation and CQV activities
for automation systems.
Strong knowledge of
ISA S88/S95 , batch processing, and GMP documentation.
Experience with
SCADA, PLC, and MES integration
preferred.
Excellent written and verbal communication skills with ability to collaborate across disciplines.
Seniority level Mid‑Senior level
Employment type Contract
Industries Pharmaceutical Manufacturing
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DeltaV Automation Engineer
to support commissioning, qualification, and validation (CQV) activities for a client in the Greater Seattle area. The ideal candidate will have hands‑on experience with Emerson DeltaV systems in GMP manufacturing environments and a solid understanding of automation life cycle documentation, validation principles, and GMP compliance.
Key Responsibilities
Support the
design, configuration, and commissioning
of DeltaV automation systems, including batch recipes, equipment modules, control strategies, and interfaces.
Develop and execute
validation protocols
(IQ/OQ/PQ) for automation systems in alignment with project timelines and regulatory requirements.
Author and review
URS, FRS, DS, CS, and testing documentation
following GAMP 5 guidelines.
Work with cross‑functional teams (Process, CQV, QA, MSAT) to ensure seamless integration of automation systems into the manufacturing process.
Provide
technical support
during system start‑up, qualification, and routine operations.
Support
change control, deviation, and CAPA
resolution related to automation and control systems.
Ensure all automation activities adhere to
21 CFR Part 11, Annex 11, and data integrity
requirements.
Qualifications
Bachelor’s degree in Engineering (Chemical, Electrical, or Automation) or related field.
5+ years of experience with
Emerson DeltaV
configuration and troubleshooting in GMP pharmaceutical or biotech environments.
Proven experience supporting
validation and CQV activities
for automation systems.
Strong knowledge of
ISA S88/S95 , batch processing, and GMP documentation.
Experience with
SCADA, PLC, and MES integration
preferred.
Excellent written and verbal communication skills with ability to collaborate across disciplines.
Seniority level Mid‑Senior level
Employment type Contract
Industries Pharmaceutical Manufacturing
#J-18808-Ljbffr