HW3
Process Controls & Automation Engineering Recruitment - USA
(Onsite | Pharmaceutical Manufacturing | GMP Environment)
Location:
On-site – Pharmaceutical Manufacturing Facility
Contract:
6–12 months (with strong potential for extension)
Start Date:
ASAP
About the Opportunity We’re partnering with a leading pharmaceutical manufacturer to hire an experienced Automation Engineer for a key on‑site contract role. This position plays a critical part in supporting and optimizing automation systems within a GMP‑regulated production environment.
The successful candidate will bring hands‑on expertise in DeltaV DCS, batch processing, and Allen‑Bradley PLCs, ensuring reliable, compliant, and efficient operation of automated systems.
Key Responsibilities
Configure, maintain, and troubleshoot DeltaV control systems for manufacturing processes.
Develop and optimize batch recipes and control logic in line with ISA‑88 standards.
Support and integrate Allen‑Bradley PLCs and associated automation equipment.
Participate in system commissioning, validation, and change control activities within a GMP framework.
Collaborate with process, QA, and IT teams to resolve automation and control issues.
Ensure all automation documentation meets GMP and regulatory compliance standards.
What We’re Looking For
Degree in Automation, Electrical, Chemical, or related Engineering discipline.
3–7+ years’ experience in automation within pharmaceutical or biotech manufacturing (GMP).
Proven experience with Emerson DeltaV DCS (configuration, troubleshooting, batch operations).
Strong background with Allen‑Bradley / Rockwell Automation PLCs and FactoryTalk.
Working knowledge of batch control (ISA‑88) and validation/qualification procedures.
Excellent troubleshooting and communication skills, with the ability to work independently on‑site.
What’s on Offer
Competitive contract rates with potential for long‑term extension.
Work with a leading pharmaceutical manufacturer at the forefront of process automation.
Opportunity to contribute to high‑impact projects in a validated GMP environment.
Collaborative, innovative, and technically advanced workplace.
Interested? If you have strong DeltaV and Allen‑Bradley experience within a GMP manufacturing environment, we’d love to hear from you!
Apply now or reach out directly for a confidential discussion.
Seniority Level
Mid‑Senior level
Employment Type
Contract
Job Function
Engineering and Manufacturing
Industries
Pharmaceutical Manufacturing, Biotechnology Research, and Hospitals and Health Care
#J-18808-Ljbffr
Location:
On-site – Pharmaceutical Manufacturing Facility
Contract:
6–12 months (with strong potential for extension)
Start Date:
ASAP
About the Opportunity We’re partnering with a leading pharmaceutical manufacturer to hire an experienced Automation Engineer for a key on‑site contract role. This position plays a critical part in supporting and optimizing automation systems within a GMP‑regulated production environment.
The successful candidate will bring hands‑on expertise in DeltaV DCS, batch processing, and Allen‑Bradley PLCs, ensuring reliable, compliant, and efficient operation of automated systems.
Key Responsibilities
Configure, maintain, and troubleshoot DeltaV control systems for manufacturing processes.
Develop and optimize batch recipes and control logic in line with ISA‑88 standards.
Support and integrate Allen‑Bradley PLCs and associated automation equipment.
Participate in system commissioning, validation, and change control activities within a GMP framework.
Collaborate with process, QA, and IT teams to resolve automation and control issues.
Ensure all automation documentation meets GMP and regulatory compliance standards.
What We’re Looking For
Degree in Automation, Electrical, Chemical, or related Engineering discipline.
3–7+ years’ experience in automation within pharmaceutical or biotech manufacturing (GMP).
Proven experience with Emerson DeltaV DCS (configuration, troubleshooting, batch operations).
Strong background with Allen‑Bradley / Rockwell Automation PLCs and FactoryTalk.
Working knowledge of batch control (ISA‑88) and validation/qualification procedures.
Excellent troubleshooting and communication skills, with the ability to work independently on‑site.
What’s on Offer
Competitive contract rates with potential for long‑term extension.
Work with a leading pharmaceutical manufacturer at the forefront of process automation.
Opportunity to contribute to high‑impact projects in a validated GMP environment.
Collaborative, innovative, and technically advanced workplace.
Interested? If you have strong DeltaV and Allen‑Bradley experience within a GMP manufacturing environment, we’d love to hear from you!
Apply now or reach out directly for a confidential discussion.
Seniority Level
Mid‑Senior level
Employment Type
Contract
Job Function
Engineering and Manufacturing
Industries
Pharmaceutical Manufacturing, Biotechnology Research, and Hospitals and Health Care
#J-18808-Ljbffr