Job Description

Overview

The Automation Engineer will manage site-wide automation and manufacturing execution systems (MES), ensuring integration, compliance, and operational excellence in a GMP-regulated environment.

Key Responsibilities

System Integration:

Oversee integration of automation systems (PLCs, SCADA, DCS) with digital applications to support production, quality, and data management.

Compliance & Validation:

Develop specifications, test protocols, and validations in line with GMP and regulatory standards.

Operational Support:

Monitor, troubleshoot, and support automation systems to maximize uptime and efficiency; provide on-call support on a rotating basis.

Risk & Compliance:

Proactively identify risks and ensure adherence to GMP, safety, and regulatory requirements.

Training & Documentation:

Create training materials, deliver staff training, and document system requirements and changes.

Collaboration:

Work closely with Manufacturing, Quality, Supply Chain, Facilities, IT, and Tech Transfer teams to align automation with business needs.

Continuous Improvement:

Identify and implement enhancements to automation systems and processes.

Standards & Best Practices:

Establish and maintain best practices for development, validation, and system governance.

About You

Experience:

4+ years in automation engineering within biopharma or related industries.

Technical Skills:

Strong knowledge of Siemens and Allen Bradley PLCs, SCADA (Aveva), DCS (DeltaV), OPC connectivity, and data integration with higher-level systems (e.g., Historian, ERP).

Soft Skills:

Strong problem-solving, collaboration, and communication skills.

Education:

Bachelors degree in Engineering, Automation, Computer Science, Biotechnology, or related technical field. *

Languages:

Proficiency in written and spoken English.