Senior DeltaV Automation Engineer

The role

This role provides technical ownership of DeltaV automation for an assigned pharmaceutical process area. You will handle functional specifications, control strategies, software development, testing, FAT, and implementation.

What you will do

• Lead DeltaV automation activities for an assigned pharmaceutical process area.
• Develop and review functional specifications, control strategies, phases, and recipes.
• Review P&IDs and define required DeltaV software changes.
• Provide technical oversight of software development and code reviews.
• Support software testing, FAT, defect resolution, and change verification.
• Coordinate with process engineering, automation, validation, and system integration teams.
• Identify technical risks and resolve automation issues.

Required qualifications

• Bachelor’s degree in Engineering or equivalent relevant experience.
• Strong Emerson DeltaV and DeltaV Batch experience.
• Pharmaceutical manufacturing experience.
• Working knowledge of ISA-88 / S88.
• GMP and validation experience.
• Experience with functional specifications, P&IDs, control strategies, phases, and recipes.
• Experience with DeltaV software/code reviews, testing, and FAT.
• Strong communication and multidisciplinary collaboration skills.

Nice to have

• 8+ years of pharmaceutical automation experience.
• API or bulk pharmaceutical manufacturing experience.
• Experience with reactors, columns, filters, or filter dryers.
• Experience developing S88 models from P&IDs.
• Experience with Parameter and Recipe Specifications.

Benefits

• paid time off
• paid holidays
• medical
• 401K match
• other unique incentives

Before you apply

• Candidates must be legally eligible to work in the United States without company sponsorship.
• Not interested in working on a corp-to-corp basis with other companies.

About the company

Valpro has several available opportunities supporting our world-class client sites or partner organizations.