Automation SME – Project Engineer

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

The Automation SME – Project Engineer is accountable for technical leadership and project coordination of assigned Automation/IT capital projects. Execution activities may be performed directly by the resource or through oversight and coordination of contractors and system integrators. As a candidate, your company must meet BMS policies, guidelines, and other requirements.

2.1. Capital Project Execution  Lead the development, planning, and execution of Automation/IT/Network Capital Projects. Act as the technical project lead for Automation/IT scope, coordinating engineering, quality, validation, IT, and vendors through all project phases.  Define project scope, schedules, cost estimates, risks, and deliverables.

Provide routine project status reporting, milestone tracking, and risk mitigation plans. Resolve complex technical and design issues arising during project execution, construction, and start‑up, ensuring decisions support regulatory compliance, safety, product quality, cost, and schedule objectives. Provide clear and timely communication on Project Engineering activities, risks, and milestones to internal stakeholders and management.

 Support Capital Appropriation Requests (CARs), budgeting, and financial tracking. Coordinate project execution activities with EHS to ensure compliance with safety, environmental, and waste‑handling requirements throughout all project phases. Review vendor quotations, develop technical specifications, and support procurement activities, including purchase requisitions and technical evaluation of equipment and services for Automation/IT capital projects.

2.2. Automation and Systems Engineering Lead and/or support the design, specification, procurement, installation, commissioning, and start-up of automation and computerized systems. Provide SME support for systems including, but not limited to: PLCs, HMI, SCADA, DCS/BAS o DeltaV, Rockwell Automation, Factory. Talk, Siemens, Wonderware o MES systems (e.

g., Syncade), data historians (OSI PI), databases (MS SQL), and virtualization platforms Review and approve automation architectures, network designs, and system configurations. Identify and promote best available automation technologies to meet site and corporate needs. 2.3. Compliance, Quality, and Validation Ensure all project activities comply with: o cGMP, FDA, EMA, OSHA, EPA/EQB o 21 CFR Part 11, Engineering, IT, and Security standards Support execution of the Computer System Validation (CSV) lifecycle, including requirements, specifications, testing, and qualification.

Support Performance Qualification (PQ) of equipment and systems installed under capital projects. Participate in quality events, including deviations, investigations, CAPAs, internal audits, and regulatory inspections related to automation systems. Ensure Automation and computerized systems are delivered in a validated state, in compliance with CSV requirements.

Support preparation, review, and execution of validation documentation. 2.4. Contractor and Vendor Management  Manage and coordinate external contractors, system integrators, and vendors.  Ensure contractor compliance with safety, environmental, security, and quality requirements.  Review technical proposals, quotations, and specifications.

 Coordinate FAT, SAT, commissioning, and start-up activities with vendors and internal stakeholders.  Ensure quality of construction, installation, and system implementation activities for Automation and related infrastructure in accordance with approved designs, specifications, and GMP requirements. 2.5. Documentation and Change Control  Develop, review, and maintain technical and project documentation, including: URS, FRS, DS, and configuration documents.

SOPs (Operations, Maintenance, Security, Backup/Restore, Disaster Recovery). Execute and support change control activities related to automation and computerized systems. Ensure proper documentation control, traceability, and data integrity. 2.6. Cross‑Functional Collaboration  Serve as the Automation Project SME for Manufacturing Business Units.

 Collaborate with Manufacturing, Quality, Engineering, Maintenance, IT, EHS, Purchasing, and Corporate teams.  Provide technical guidance to resolve complex operational and project-related issues.  Support client initiatives by ensuring adherence to Project Management processes and governance.

REQUIREMENTS

& QUALIFICATIONS Required The assigned resource must meet the following minimum qualifications:  Bachelor’s degree in Engineering, Computer Science, Information Systems, or related field.  Minimum five (5) years of experience in pharmaceutical operations or manufacturing environments with proven project management experience, of which: o At least four (4) years must be in process automation within a pharmaceutical environment o At least two (2) years must be in computerized systems validation (CSV).

 Demonstrated proficiency in computer system lifecycle concepts, change control processes, and FDA regulatory requirements, including 21 CFR Part 11.  Proven experience developing and reviewing Computerized Functional Requirements (CFR/URS) and Design Specifications (DS/FRS).  In-depth knowledge of the design, installation, commissioning, and qualification of computerized systems, PLCs, and automation platforms in pharmaceutical manufacturing.

 Broad knowledge of cGMPs, FDA, EMA, and applicable regulatory guidelines for biopharmaceutical manufacturing facilities.  Experience supporting internal and external regulatory audits (e.g., FDA, EMA).  Strong understanding of pharmaceutical manufacturing processes, equipment, and automation systems.  Knowledge of electrical controls theory, mechanical concepts, and electronic circuitry, with ability to read and interpret electrical and mechanical drawings.

 Proven skills in project management, systems development, and implementation of manufacturing automation, MES, and quality-related systems.  Experience with PLC programming platforms, data acquisition systems, historians (e.g., OSI PI), databases (e.g., MS SQL), and industrial networking infrastructures.  Ability to review and support development of SOPs and work instructions.

 Strong analytical and problem-solving skills, with ability to resolve complex technical issues based on data.  Fully bilingual English/Spanish, written and verbal.  Strong interpersonal skills with ability to work effectively across all organizational levels and disciplines.  Ability to manage and prioritize multiple complex activities simultaneously.

 Self-starter, well organized, flexible, and able to meet deadlines.  Willingness to work irregular hours, weekends, and holidays as required.  Ability to exercise good judgment. Preferred Experience with CMMS systems (e.g., Maximo). High level of expertise in Rockwell Automation platforms. Experience with Siemens, Wonderware, and Factory.

Talk Batch. Experience with virtualization platforms (VMware v. Sphere). Experience with MES systems (e.g., Syncade). Experience with OSIsoft / AVEVA PI systems and Microsoft SQL databases. SKILLS Technical Skills PLCs, HMI, SCADA, DeltaV, Factory. Talk — advanced configuration and troubleshooting MES systems — support and integration Change control execution and CAPA support in regulated environments Automation procedure development — SOPs, security plans, backup/restore, disaster recovery cGMP, 21 CFR Part 11, and Data Integrity compliance Quality event investigation and internal audit support Network configuration and industrial communication protocols Microsoft Office 365 Soft Skills Deep technical ownership of automation systems Clear communication with Manufacturing, Quality, IT, and Engineering teams Proactive risk identification and escalation Disciplined in regulatory documentation and change management Project milestone accountability Consulting mindset — advising on technology use and process improvement