 
        
        Overview
Consult Pirbright, England, United Kingdom
Direct message the job poster from Consult
Location: Woking Area
Type: Full-Time, Contract (On-site)
We’re seeking an Automation Engineer to take on a newly created role that will directly impact production efficiency, compliance, and innovation. In this position, you’ll maintain and evolve site automation technologies - from production equipment to building systems - while collaborating with global teams and leading key projects. This is a fantastic opportunity to combine hands-on technical expertise with strategic project leadership in a dynamic, regulated environment.
Key Responsibilities
 * Drive Innovation: Support small capital and expense projects that enhance automation capability in line with global standards.
 * Maintain Systems: Troubleshoot and manage building automation systems, ensuring lifecycle management and compliance with site SOPs.
 * Collaborate Globally: Work with international teams to deliver automation solutions and provide data to guide investment.
 * Lead Projects: Act as the automation lead on projects and continuous improvement initiatives.
 * Support Operations: Minimise production downtime by supporting day-to-day automation needs, implementing CAPAs, and maintaining documentation such as network drawings and asset registers.
 * Research & Train: Explore new technologies, adopt them effectively, and provide training to others post-implementation.
What We’re Looking For
Education & Experience: Bachelor’s degree in Engineering or Control Systems, plus 2+ years’ relevant experience.
Technical Skills:
 * Low voltage controls (relays, safety circuits, drives).
 * Device interfaces (sensors, IO modules, fieldbus, networking).
 * PLC programming (ladder, function block, structured text).
 * HMI/SCADA systems.
Additional Skills:
 * Understanding of building automation systems.
 * Strong communication and project management abilities.
 * Basic awareness of OT cybersecurity.
Industry Knowledge: Familiarity with biopharmaceutical regulations and GMP is advantageous.
Seniority level
 * Mid-Senior level
Employment type
 * Full-time
Job function
 * Information Technology and Manufacturing
Industries
 * Pharmaceutical Manufacturing
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