Job Description
Job Description
About Company:
JC Automation Corp. (JCA) was founded in 1997 with the mission of filling a gap between technology and regulatory requirements in the life science manufacturing industry. The company offers highly capable resources at an affordable cost to build solutions and execute projects in: Automation, Control Systems Integration, Information Technology, System Integration and Regulatory Compliance.
JCA is a HUBZone Certified Small Business Firm, NMSDC Certified Minority Business Enterprise, and Certified Critical Industry Supplier. It’s mission is to add value by delivering quality services & solutions on time all the time by transforming processes & technology into business advantages.
ABOUT THE ROLE
We are seeking an experienced Automation Engineer to support automation and controls activities for capital projects within a regulated pharmaceutical manufacturing environment. This role combines hands-on technical expertise with cross-functional project coordination, ensuring reliable system integration, commissioning, and execution support throughout the project lifecycle.
The ideal candidate brings proven experience with industrial control systems, strong troubleshooting capabilities, and the ability to work effectively across engineering, validation, and operations teams in a fast-paced GMP environment.
RESPONSIBILITIES
- PLC, HMI & SCADA Support: Support PLC, HMI, and SCADA system integration, configuration, and troubleshooting across capital project activities. Ensure control systems meet design specifications and operational requirements prior to and during deployment.
- Automation Design & Modification Support: Assist with automation design reviews and support control system modifications, ensuring changes are properly documented, reviewed, and implemented in accordance with project and regulatory requirements.
- Commissioning & Startup Support: Support FAT (Factory Acceptance Testing), SAT (Site Acceptance Testing), commissioning, and startup activities, ensuring systems are properly tested, validated, and handed over to operations.
- Cross-Functional Coordination: Coordinate with engineering, validation, quality, and operations teams throughout the project lifecycle to ensure alignment, timely execution, and compliance with GMP and safety requirements.
- Field Investigations & Issue Resolution: Support field investigations, testing activities, and resolution of system issues during project execution and commissioning phases, applying structured troubleshooting methodologies.
- Documentation & Records: Maintain automation documentation, system backups, and technical records in compliance with GMP, data integrity, and project standards. Ensure all changes are captured and traceable throughout the project lifecycle.
REQUIREMENTS & QUALIFICATIONS
Required
- Bachelor's degree in Electrical, Computer, Mechanical Engineering, or a related technical field.
- Minimum 3 years of experience in automation or controls engineering in industrial or pharmaceutical environments.
- Hands-on experience with PLC, HMI, SCADA, or industrial control systems in an integration or project support capacity.
- Strong troubleshooting and technical problem-solving skills in automation and controls systems.
- Experience supporting capital or industrial projects including FAT, SAT, and commissioning activities.
- Familiarity with GMP regulations and validation activities in regulated manufacturing environments.
Preferred
- Experience with Allen-Bradley (Rockwell), Siemens, DeltaV, or similar automation platforms.
- Exposure to pharmaceutical or biotech manufacturing environments.
- Bilingual in English and Spanish (oral and written).
- PMP or equivalent project management certification.
SKILLS
Technical Skills
- PLC, HMI, and SCADA systems — integration, configuration, and troubleshooting
- Allen-Bradley (Rockwell), Siemens, DeltaV, or equivalent automation platforms
- FAT / SAT / commissioning and startup support
- Automation design review and control system modification
- Field investigations and structured troubleshooting
- GMP compliance and validation activities in regulated environments
- Technical documentation and automation records management
- Microsoft Office 365
Soft Skills
- Strong cross-functional collaboration with engineering, validation, quality, and operations teams
- Proactive problem-solving and root cause analysis mindset
- Ability to manage multiple priorities in a fast-paced project environment
- Clear and accurate technical communication — written and verbal
- Results-oriented with strong attention to detail and accountability
- Adaptable and reliable in dynamic capital project environments