Senior Automation Engineer
Key Skills
Job Description
Company Overview A leading organization within the manufacturing sector dedicated to delivering high-quality, innovative solutions. The company values technical excellence, teamwork, and continuous improvement to ensure operational success and sustainability. Job Description We are seeking a proactive and experienced Senior Automation Engineer to join our dynamic team in Breda. This role focuses on overseeing automation systems involved in the installation, commissioning, and lifecycle management of advanced manufacturing equipment, particularly in device assembly, inspection, labeling, and packaging areas. The ideal candidate will ensure equipment reliability, security, and optimal performance through expert automation practices. Responsibilities Manage automation aspects of new equipment installations and upgrades, ensuring alignment with project timelines. Support New Product Introduction (NPI) and coordinate test phases at equipment vendors and on-site. Oversee automation design, including review and creation of technical documents such as URS, FDS, HDS, and SDS. Support equipment installation, testing, commissioning, and validation, considering network security settings. Ensure equipment security using Amgen standards and support the connection to data historians like PI. Participate in FAT, commissioning, and qualification activities. Conduct automation preventive maintenance and data integrity assessments. Advise on spare parts and develop asset spare parts lists for automation equipment. Create backup and restore procedures, parameter review protocols, and audit trail review procedures. Support automation training for Maintenance, Engineering, and Operators. Provide operational hypercare support and update documentation to maintain operational effectiveness. Requirements Bachelor’s or master’s degree in Industrial Automation Engineering or related fields. Minimum of 5 years’ experience in process control and information systems support within biopharmaceutical or pharmaceutical manufacturing environments. Proven ability to execute independent projects in cross-functional, global teams. Hands-on experience with labelling and packaging equipment, including PLC, HMI, SCADA, Cognex vision systems, and industrial PCs. Familiar with regulated environments (GMP, OSHA, EPA). Strong knowledge of automation standards, network security, and data management. Excellent communication skills in English, both written and spoken. Ability to work outside regular hours when necessary. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.
Core Responsibilities
Oversee automation for manufacturing equipment installations, upgrades, testing, commissioning, qualification, and lifecycle management, including security and data historian connectivity. Develop and maintain automation documentation and procedures, support preventive maintenance and data integrity, advise on spare parts, train users, and provide operational support.
Requirements
Requires a bachelor’s or master’s degree in Industrial Automation Engineering or a related field and at least five years of process control and information systems experience in pharmaceutical or biopharmaceutical manufacturing. Candidates should have hands-on experience with packaging and labeling equipment and PLC, HMI, SCADA, Cognex vision systems, and industrial PCs, along with knowledge of regulated environments, automation standards, network security, and data management.
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