What are the responsibilities and job description for the Controls Engineer 3 position at BioTalent?
Job Title
Senior Controls & Automation Engineer
Position Summary
The Senior Controls & Automation Engineer is responsible for leading and supporting manufacturing automation systems, process control improvements, and capital projects within a GMP manufacturing environment. This role serves as the Controls Subject Matter Expert (SME) for manufacturing operations, technical transfers, troubleshooting activities, process improvements, and regulatory inspections. The position works cross-functionally with Manufacturing, Engineering, Quality, Validation, and Technical Operations to ensure reliable operation of process automation systems while driving continuous improvement initiatives.
Key Responsibilities
Project Execution & Process Improvement
- Lead the planning, design, execution, and implementation of plant projects involving complex equipment modifications and significant process improvements.
- Serve as the Controls Lead for technology transfer projects, ensuring successful integration of automation systems into manufacturing operations.
- Support commissioning, qualification, and startup activities for new equipment and automation systems.
- Drive continuous improvement initiatives focused on reliability, performance, efficiency, and process robustness.
Automation & Controls Support
- Provide technical leadership and SME support for the design, operation, maintenance, and optimization of process automation systems and manufacturing equipment.
- Support resolution of equipment breakdowns, production issues, deviations, and product quality concerns related to automation systems.
- Conduct troubleshooting and root cause investigations for manufacturing process control systems, including PLCs, HMIs, SCADA systems, historians, and networked automation equipment.
- Analyze process and equipment performance using PI Historian data, control system trends, and automation analytics.
- Review, troubleshoot, and modify automation code and configurations as required.
- Participate in an on-call support rotation and provide technical support during off-hours as necessary.
Compliance, Quality & Change Management
- Initiate, manage, and support change controls throughout the full lifecycle, ensuring compliance with GMP and company requirements.
- Own and execute corrective and preventive actions (CAPAs) related to automation and controls systems.
- Support deviation investigations and implement corrective solutions.
- Review and approve SOPs, Functional Specifications, Work Instructions, and engineering documentation.
- Ensure all activities are performed in accordance with GMP, safety, quality, and regulatory requirements.
Cross-Functional Collaboration
- Represent the Controls function in Integrated Project Teams (IPT), Joint Project Teams (JPT), and cross-functional meetings.
- Collaborate with Manufacturing, Facilities, Quality, Validation, and Engineering teams to support operational excellence.
- Provide technical guidance and training on automation systems to manufacturing and support personnel.
Regulatory & Inspection Support
- Participate in internal audits, customer audits, and regulatory inspections as the Controls SME.
- Provide technical documentation and responses during audit and inspection activities.
- Ensure automation systems remain compliant with applicable regulatory requirements and data integrity standards.
Safety & Training
- Perform all work safely and follow Environmental Health & Safety (EHS) requirements.
- Complete all required training and maintain qualifications relevant to assigned responsibilities.
- Remain current on industry best practices, emerging technologies, and company procedures.
Required Qualifications
- Bachelor's degree in Electrical Engineering, Chemical Engineering, Automation Engineering, Computer Engineering, or related technical discipline.
- 5 years of experience supporting automation and process control systems in a regulated manufacturing environment.
- Experience with pharmaceutical, biotechnology, life sciences, or GMP manufacturing operations.
- Strong knowledge of PLC, HMI, SCADA, and Historian systems.
- Experience with troubleshooting automation systems and supporting manufacturing operations.
- Knowledge of change control, CAPA, deviation management, and GMP documentation practices.
- Excellent analytical, problem-solving, and communication skills.
Preferred Qualifications
- Experience with DeltaV, Rockwell Automation, Siemens, or other distributed control systems.
- Experience with OSIsoft PI Historian and process data analytics.
- Knowledge of GAMP 5, 21 CFR Part 11, and computerized system validation (CSV).
- Project management experience supporting capital projects and technical transfers.
- Experience supporting regulatory inspections (FDA, EMA, MHRA, etc.).
Key Competencies
- Technical Leadership
- Automation & Controls Expertise
- Root Cause Analysis
- Project Execution
- Continuous Improvement
- GMP Compliance
- Stakeholder Management
- Cross-Functional Collaboration
- Risk Assessment & Problem Solving
- Effective Communication