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.

Job Summary:
The Automation Project Manager is responsible for leading the planning, execution, and delivery of Automation and IT capital projects within a cGMP-regulated environment. This role serves as the technical lead, ensuring successful project implementation while maintaining compliance with regulatory requirements and quality standards.

Key Responsibilities:

• Lead the development, planning, and execution of Automation/IT capital projects from initiation through completion.
• Act as the technical lead, coordinating cross-functional teams including Engineering, Quality, Validation, IT, and external vendors.
• Provide subject matter expertise (SME) for automation systems including PLCs, SCADA, DeltaV, and MES (e.g., Syncade).
• Manage project scope, timelines, resources, and deliverables to ensure successful execution.
• Ensure compliance with cGMP regulations, FDA requirements, and 21 CFR Part 11.
• Support and oversee Computer System Validation (CSV) lifecycle activities, including documentation and testing.
• Identify and manage project risks, issues, and change controls.
• Facilitate communication and alignment across stakeholders throughout the project lifecycle.
• Ensure proper documentation, reporting, and project closeout activities are completed.

Requirements:

• Bachelor’s degree in Engineering, Computer Science, or related field.
• Experience managing automation and/or IT projects in regulated environments (pharma/biotech preferred).
• Strong knowledge of automation systems (PLC, SCADA, DCS, MES).
• Experience with Computer System Validation (CSV) and regulatory compliance (cGMP, FDA, 21 CFR Part 11).
• Proven ability to lead cross-functional teams and manage external vendors.
• Strong project management, communication, and problem-solving skills.
• PMP or similar certification is a plus.
• Must be authorized to work in the United States without sponsorship.

Location:

• Puerto Rico