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Senior Automation Engineer

SIRE® Life Sciences 🧬

Breda
Full-time
2-5 years experience
On-site

Key Skills

Automation Engineering
PLC-Controlled Systems
HMI
SCADA
Industrial PCs
Vision Systems
Cognex
Equipment Commissioning
Troubleshooting
FAT
Equipment Qualification
GMP
Data Integrity
PI Data Historian
Technical Documentation
Project Coordination

Job Description

About the Company An international biopharmaceutical organization with a modern manufacturing site in Breda, investing in advanced automation technologies and the expansion of its production capabilities. Role Description As a Senior Automation Engineer, you will support the implementation, commissioning, and lifecycle management of automated manufacturing equipment across device assembly, inspection, labelling, and packaging. You will provide advanced technical support for automation-related production issues and contribute to new equipment projects, ensuring reliable, secure, and efficient systems. Key Responsibilities Lead automation activities for new equipment, upgrades, and manufacturing projects. Develop and review technical documentation, including URS, FDS, HDS, and Software Design Specifications (SDS). Support equipment installation, testing, commissioning, FAT, and qualification activities. Troubleshoot complex automation issues and provide advanced technical support to manufacturing and maintenance teams. Work with PLCs, HMIs, SCADA, Industrial PCs, and vision systems such as Cognex. Implement automation standards, security requirements, monitoring tools, and backup/restore procedures. Maintain equipment parameter lists, audit trail review procedures, and work instructions. Support data integrity assessments and connections to the PI data historian. Coordinate with cross-functional engineering teams, vendors, and project stakeholders. Provide automation training and operational support to maintenance, engineering, and production teams. Requirements 4+ years of Automation Engineering experience supporting automated manufacturing equipment. Strong practical knowledge of PLC-controlled systems and experience with HMI, SCADA, and Industrial PCs. Experience with manufacturing equipment and production lines; labelling and packaging experience is particularly relevant. Experience with equipment installation, commissioning, troubleshooting, and technical project execution. Familiarity with regulated environments, such as GMP, is a strong advantage. Ability to work independently and collaborate with multidisciplinary, international teams. Strong analytical, communication, and problem-solving skills. Fluent in English and flexible to occasionally work outside standard office hours.

Core Responsibilities

Lead automation work for new equipment, upgrades, and manufacturing projects, including documentation, installation, testing, commissioning, FAT, and qualification. Troubleshoot production automation issues, maintain secure and reliable systems, support data integrity and historian connections, and train and assist cross-functional teams.

Requirements

Requires at least four years of experience supporting automated manufacturing equipment, with practical knowledge of PLC systems, HMI, SCADA, and Industrial PCs. Manufacturing line experience, commissioning and troubleshooting skills, and the ability to work independently and collaboratively are required; GMP familiarity is an advantage.

About SIRE® Life Sciences 🧬

Industry: Biotechnology Research

Company size: 201-500 employees

SIRE® Life Sciences is the market-leading partner for Life Sciences consultancy, project management, and secondment services in the Netherlands. We specialize in connecting expert consultants and project managers with leading biotech, pharmaceutical, medical device, clinical research, and food technology organizations. Our services include: - Life Sciences recruitment & executive search - Interim management & secondment - SOW-based project outsourcing & delivery - RPO (Recruitment Process Outsourcing) - MSP workforce management & vendor-neutral solutions - GMP, GCP, GLP compliance staffing - Clinical research & regulatory affairs resourcing With 100,000+ professionals in our network and 25+ years of experience, SIRE® Life Sciences delivers measurable results for regulated organizations across the Netherlands and Europe. We work with pharma, biotech, medical device, CDMO, CRO, and food technology companies at every stage of the product lifecycle. What sets us apart: - Deep domain expertise in Life Sciences & regulated industries - Full compliance with GxP, ISO, WAADI, and Dutch labour law - Flexible engagement models: permanent, interim, project (SOW), and managed services - Proven delivery track record across Pharma, Biotech, MedTech & Food Science Based in Leiden Bio Science Park, Netherlands. www.sire-search.com

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