Automation Engineer

Hamlyn Williams; Chapel Hill (NC); On-site; USD 166,000 - 250,000; Full time

Job summary

A leading company in the pharmaceutical sector is seeking an Automation Engineer with expertise in DeltaV systems. The role involves designing and supporting automation solutions in a GMP-compliant environment. Ideal candidates will have strong communication and problem-solving skills, along with a solid background in batch automation. Join a team dedicated to innovation and compliance in life-saving production.

Qualifications

• 5+ years of hands-on experience with DeltaV in a GMP-regulated environment.
• Proven knowledge of GMP, GAMP5, and electronic records compliance.

Responsibilities

• Design, configure, and support Emerson DeltaV control systems.
• Lead project lifecycle deliverables: URS, FDS, SDS, FAT, SAT.
• Troubleshoot and maintain system performance in line with GAMP5.

Skills

Communication

Teamwork

Problem Solving

Education

Bachelor’s degree in Engineering

Bachelor’s degree in Automation

Tools

DeltaV

Job description

This range is provided by Hamlyn Williams. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$80.00/hr - $120.00/hr

Direct message the job poster from Hamlyn Williams

Process Controls & Automation Engineering (Contract) - USA

Job Title: Automation Engineer (Pharma | GMP)

Are you an experienced DeltaV Automation Engineer looking to make an impact in a regulated pharmaceutical environment? We’re hiring a DeltaV Specialist with strong knowledge of Emerson’s DeltaV DCS, GMP compliance, and batch automation to join our high-performing team.

What You’ll Do:

• Design, configure, and support Emerson DeltaV control systems for pharmaceutical manufacturing processes
• Work across cross-functional teams to develop and implement GMP-compliant automation solutions
• Lead and contribute to project lifecycle deliverables: URS, FDS, SDS, FAT, SAT, commissioning, and validation
• Support batch process automation (ISA-88) and recipe development within the DeltaV system
• Troubleshoot, optimize, and maintain system performance in line with GAMP5 and 21 CFR Part 11 standards
• Author and maintain system documentation, SOPs, and change control records
• Collaborate with Quality, Validation, and IT teams to ensure data integrity and compliance

What You Bring:

• Bachelor’s degree in Engineering, Automation, or related field
• 5+ years of hands-on experience with DeltaV in a GMP-regulated pharmaceutical environment
• Proven knowledge of GMP, GAMP5, and electronic records compliance
• Experience with batch automation, alarm management, and lifecycle documentation
• Strong communication, teamwork, and problem-solving skills
• Bonus: DeltaV Certification, experience with MES/ERP integration, or DeltaV version upgrades

Why Apply?

You'll be working on cutting-edge automation systems that support life-saving pharmaceutical production, in an environment that values compliance, innovation, and collaboration. If you're passionate about automation in a regulated industry, this is the place for you.