Jobdetails For one of our clients, an international pharmaceutical company, we are seeking a Senior Automation Engineer (Biotech Process Automation).
General Information: Start date: 01.10.2025 Duration: 12 months with the possibility of extension Workplace: Schachen, Luzern Home office: 100% onsite, some home office days are possible after approval Workload: 100%Working hours: Standard...
Your Profile: You are a seasoned professional with at least 5 years of experience in automation controls, specifically with Delta V.
You have a proven track record of working in a c GMP or other highly regulated industry, such as Biologics, Medical Devices, or Food.
You're not just an engineer; you're an expert in computer validation (GAMP 5) and change control, with a strong understanding of ISA S95 and S88.
Tasks & Responsibilities: Serve as a Subject Matter Expert for the implementation of control strategies for new equipment to enhance manufacturing processes in a Good Manufacturing Practice (GMP) environment Implement innovative technologies, software, control strategies, and instruments to streamline processes and reduce the effort involved in manufacturing and administrative processes Provide key automation support for various manufacturing systems such as DCS (Delta V), MES(PAS-X), PLC, SCADA, and OEM systems Support and/or Direct Continuous Improvement projects with automation review of equipment specifications, P&IDs, and System Life Cycle documentation Responsible for troubleshooting challenging equipment/automation issues to improve manufacturing performance (e.g.
yield improvements, etc.), changes to support new products, and maintaining the automation systems in compliance with c GMPTransfer of Process Technologies from early-stage pipeline facilities and drive to GMP Operational Status, and support line of sight to commercial supply Lead automation related investigations into deviations and implement corrective actions.
Inspire Diversity and Inclusion – building effective working relationships within a cross functional team across different cultures and backgrounds Working with external companies, organizing spare parts and service visits Supporting the qualification of new systems.
Write, review, and/or execute test documents.
Collaborates within the Operations, Quality, Validation and Technical organizations to resolve complex problems Participate and actively support Digital Transformation initiatives involving system integrations, data connectivity, data analysis/modelling, validation methods and value-based optimization of manufacturing via process control system Limited off shift work may be required to meet project, operations, and qualification needs Requirements: Bachelor’s degree in a Life Science discipline or equivalent practical experience of at least 5 years of experience in automation controls (Delta V DCS)Thorough knowledge of computer validation/SDLC requirements and automation change control procedures (e.g., GAMP 5)Effective oral / written communication skills in English (C1), German is nice to have Proven experience with Delta V DCS, Delta V Batch, including the ISA S95 and S88 At least 3 years of experience in Automation or Engineering function for Biologics, Food, Medical Devices, or Pharmaceutical industries Proven experience with development and implementation of industrial controls such as DCS (Delta V), MES (PAS-X), Historian (PI)I/O Networking experience (i.e.
Ethernet/IP, OPC, Profinet, and Mod Bus protocols) is advantageous Basic networking experience Commissioning and qualification, test protocol development and execution.
Sound interesting? Apply Now - we are looking forward to receiving your application.mehr anzeigen For one of our clients, an international pharmaceutical company, we are seeking a Senior Automation Engineer (Biotech Process Automation).
General Information: Start date: 01.10.2025 Duration: 12 months with the possibility of extension Workplace: Schachen, Luzern Home office: 100% onsite, some home office days are possible after approval Workload: 100%Working hours: Standard Your Profile: You are a seasoned professional with at least 5 years of experience in automation controls, specifically with Delta V.
You have a proven track record of working in a c GMP or other highly regulated industry, such as Biologics, Medical Devices, or Food.
You're not just an engineer; you're an expert in computer validation (GAMP 5) and change control, with a strong understanding of ISA S95 and S88....
Tasks & Responsibilities: Serve as a Subject Matter Expert for the implementation of control strategies for new equipment to enhance manufacturing processes in a Good Manufacturing Practice (GMP) environment Implement innovative technologies, software, control strategies, and instruments to streamline processes and reduce the effort involved in manufacturing and administrative processes Provide key automation support for various manufacturing systems such as DCS (Delta V), MES(PAS-X), PLC, SCADA, and OEM systems Support and/or Direct Continuous Improvement projects with automation review of equipment specifications, P&IDs, and System Life Cycle documentation Responsible for troubleshooting challenging equipment/automation issues to improve manufacturing performance (e.g.
yield improvements, etc.), changes to support new products, and maintaining the automation systems in compliance with c GMPTransfer of Process Technologies from early-stage pipeline facilities and drive to GMP Operational Status, and support line of sight to commercial supply Lead automation related investigations into deviations and implement corrective actions.
Inspire Diversity and Inclusion – building effective working relationships within a cross functional team across different cultures and backgrounds Working with external companies, organizing spare parts and service visits Supporting the qualification of new systems.
Write, review, and/or execute test documents.
Collaborates within the Operations, Quality, Validation and Technical organizations to resolve complex problems Participate and actively support Digital Transformation initiatives involving system integrations, data connectivity, data analysis/modelling, validation methods and value-based optimization of manufacturing via process control system Limited off shift work may be required to meet project, operations, and qualification needs Requirements: Bachelor’s degree in a Life Science discipline or equivalent practical experience of at least 5 years of experience in automation controls (Delta V DCS)Thorough knowledge of computer validation/SDLC requirements and automation change control procedures (e.g., GAMP 5)Effective oral / written communication skills in English (C1), German is nice to have Proven experience with Delta V DCS, Delta V Batch, including the ISA S95 and S88 At least 3 years of experience in Automation or Engineering function for Biologics, Food, Medical Devices, or Pharmaceutical industries Proven experience with development and implementation of industrial controls such as DCS (Delta V), MES (PAS-X), Historian (PI)I/O Networking experience (i.e.
Ethernet/IP, OPC, Profinet, and Mod Bus protocols) is advantageous Basic networking experience Commissioning and qualification, test protocol development and execution.
Sound interesting? Apply Now - we are looking forward to receiving your application.mehr anzeigen