Rockwell Automation Engineer
Role summary
Rockwell Automation Engineer needed for a large-scale automation upgrade project in pharmaceutical manufacturing. This hands-on, onsite role involves migrating legacy systems to modern Rockwell FactoryTalk platforms. Responsibilities include PLC/HMI programming, system design, troubleshooting, GMP documentation, and supporting validation activities within a regulated environment. Requires strong expertise in Rockwell tools and automation engineering.
Job Title: Rockwell Automation Engineer
Industry: Pharmaceutical Manufacturing Industry
Location: Troy, NY (100% Onsite)
Job Summary
We are seeking experienced Rockwell Automation Engineers to support a large-scale automation upgrade project within the pharmaceutical industry. The role involves transitioning existing manufacturing suites from legacy systems to modern Rockwell FactoryTalk platforms. This is a hands-on, onsite position requiring strong expertise in automation, controls engineering, and programming within GMP-regulated environments.
Key Responsibilities:
- Lead and support the migration of legacy automation systems (including older Rockwell and other platforms) to Rockwell FactoryTalk.
- Design, develop, and implement automation solutions for pharmaceutical manufacturing suites.
- Perform PLC/HMI programming, coding, and system configuration using Rockwell technologies.
- Troubleshoot and optimize control systems to ensure reliable and efficient operations.
- Collaborate with cross-functional teams including production, quality, and validation.
- Develop and maintain GMP-compliant documentation (URS, FS, DS, IQ/OQ protocols, etc.).
- Support commissioning, qualification, and validation activities.
- Ensure compliance with industry regulations and internal quality standards.
Required Skills & Qualifications:
- Strong experience with Rockwell Automation tools and platforms.
- Mandatory hands-on experience with Rockwell FactoryTalk.
- Proven background in automation engineering, controls engineering, and programming/coding.
- Experience working with legacy systems and system upgrades/migrations.
- Knowledge of PLCs, HMIs, and SCADA systems.
- Familiarity with GMP documentation and regulated environments (pharma preferred).
- Strong problem-solving and troubleshooting skills.
- Excellent communication and teamwork abilities.
Preferred Qualifications:
- Experience in pharmaceutical or life sciences manufacturing environments.
- Prior experience with system integration and large-scale automation rollouts.
- Understanding of validation processes and compliance standards.
