Process Automation Engineer, Manufacturing Engineering

St. Louis, MO, US • Posted 1 day ago • Updated 8 hours ago
Full Time
On-site
Fitment

Dice Job Match Score™

🎯 Assessing qualifications...

Job Details

Skills

  • Process Automation
  • Manufacturing Engineering
  • IT Management
  • Technical Support
  • Operational Efficiency
  • Systems Design
  • PQ
  • Lifecycle Management
  • Process Control
  • Data Acquisition
  • Regulatory Compliance
  • Software Development Methodology
  • Licensing
  • Cyber Security
  • URS
  • FRS
  • SDS
  • IQ
  • OQ
  • Documentation
  • MES
  • Reporting
  • Auditing
  • Electrical Engineering
  • Computer Engineering
  • Computer Science
  • Pharmaceutics
  • Medical Devices
  • Siemens
  • Startups
  • Change Control
  • Programmable Logic Controller
  • Ladder Logic
  • Computer Networking
  • TCP/IP
  • VLAN
  • Firewall
  • Switches
  • SQL
  • Database
  • Manufacturing
  • Data Integration
  • Data Integrity
  • SCADA
  • Problem Solving
  • Conflict Resolution
  • Communication
  • Collaboration
  • Management
  • GMP
  • FOCUS
  • Continuous Improvement
  • Health Care
  • Innovation
  • PASS
  • Screening

Summary

Work Schedule
Standard (Mon-Fri)

Environmental Conditions
Office

Job Description

The Process Automation Engineer is a key member of the site Engineering team, reporting to the Manufacturing Engineering Automation Manager. This role is responsible for supporting and enhancing the site's Operational Technology (OT) infrastructure and automation systems used in GMP manufacturing.

You will provide technical leadership for process control systems, support manufacturing equipment reliability, and lead automation initiatives that improve system performance, data visibility, compliance, and operational efficiency.

This role also supports capital projects, including system design and review, installation, commissioning, qualification (IQ/OQ/PQ), and lifecycle management. Success requires strong technical expertise, cross-functional collaboration, and structured problem-solving in a regulated environment.

What will you do?
  • Design, implement, and maintain process control systems in compliance with corporate standards and site GMP requirements.
  • Provide technical ownership of DeltaV, PLC, SCADA, and associated automation platforms.
  • Lead troubleshooting efforts for control systems, networked devices, and data acquisition platforms.
  • Develop and implement system enhancements to improve equipment reliability, throughput, and data integrity.
  • Ensure compliance with software lifecycle management, patching strategies, licensing, and cybersecurity standards.
  • Support validation documentation including URS, FRS, SDS, IQ/OQ protocols, and change control documentation.
  • Integrate manufacturing data sources (PLCs, historians, MES, etc.) to improve operational visibility and reporting.
  • Develop monitoring and alerting tools to proactively detect system issues.
  • Participate in and support regulatory inspections and audits.
  • Collaborate with Corporate IT to maintain secure and compliant OT/IT network integration.
  • Provide on-call support for critical manufacturing systems as required.

How will you get here?
  • Bachelor's degree in Electrical Engineering, Computer Engineering, Computer Science, or related technical field is highly preferred. Associate Degree or equivalent is required.
  • Equivalent combination of education and relevant experience may be considered.
  • 3+ years of experience supporting automation systems in a regulated manufacturing environment (pharmaceutical, biotech, medical device preferred).
  • Hands-on experience with DCS and PLC platforms (DeltaV, Rockwell, Siemens, etc.).
  • Experience with system commissioning, loop tuning, and startup activities.
  • Experience supporting GMP change control and validation processes.

Technical Knowledge
  • Strong understanding of PLC and DCS programming, including ladder logic and function block programming.
  • Knowledge of industrial networking (TCP/IP, VLANs, firewalls, managed switches).
  • Experience with data historians, SQL databases, and manufacturing data integration.
  • Familiarity with 21 CFR Part 11, data integrity principles, and GMP automation requirements.
  • Experience with SCADA system configuration and maintenance.
  • Understanding of ISA-88 batch control concepts (preferred).

Behavioral Competencies
  • Demonstrated ability to lead technical problem-solving efforts.
  • Strong communication and cross-functional collaboration skills.
  • Ability to prioritize and manage multiple projects in a fast-paced GMP environment.
  • Proactive mindset with focus on continuous improvement.

Benefits

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

Other

Relocation assistance is not provided.

Must be legally authorized to work in the United States now and in the future, without sponsorship.

Must be able to pass a comprehensive background check, which includes a drug screening.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 10286239
  • Position Id: 936f9a1c76b02aed0d6ac0eee2c7c9c4
  • Posted 1 day ago
Create job alert
Set job alertNever miss an opportunity! Create an alert based on the job you applied for.

Similar Jobs

St. Louis, Missouri

Today

Full-time

St. Louis, Missouri

Today

Full-time

USD 68,100.00 - 102,100.00 per year

St. Louis, Missouri

Today

Full-time

Roxana, Illinois

Today

Full-time

USD 124,200.00 - 151,800.00 per year

Search all similar jobs