Automation Engineer (MES / Syncade)

m/f/d,

Job Profil (8IRE61)

Life Sciences - Engineering
Contracting
Vollzeit
23.11.2026 - 22.11.2027
Emerson Syncade MES, GMP, eBR, P&ID, CIP/SIP

Drive Digital Excellence in Biopharmaceutical Manufacturing

We are seeking an experienced Automation Engineer (MES / Syncade) to support the delivery of manufacturing digitalization and automation initiatives within a highly regulated biopharmaceutical production environment.

In this role, you will contribute to the implementation, optimization, and support of Manufacturing Execution Systems (MES) and Electronic Batch Records (eBR), working closely with multidisciplinary teams across engineering, manufacturing, quality, validation, and operations. This is an exciting opportunity to play a key role in enhancing manufacturing efficiency, compliance, and operational performance.

Key Facts

Position: Automation Engineer (MES / Syncade)
Location: Valais, Switzerland
Work Model: On-site
Contract Type: Contractor
Duration: 12 months with potential extension
Workload: Full-time (41 hours per week)
Industry: Biopharmaceutical Manufacturing
Language: Fluent English required

Your Responsibilities

MES & Automation Project Delivery

Support the delivery of MES and automation work packages throughout the project lifecycle
Participate in process design, configuration, testing, commissioning, qualification, and production support activities
Collaborate with engineering, automation, validation, quality, and operations teams to ensure successful project execution
Ensure project deliverables meet quality, compliance, and timeline expectations

Emerson Syncade & Electronic Batch Records (eBR)

Design, configure, test, deploy, and maintain Electronic Batch Records (eBR) using Emerson Syncade
Perform troubleshooting, root cause analysis, and system enhancements under change control procedures
Support User Acceptance Testing (UAT), commissioning, qualification, and go-live activities
Provide ongoing production support and continuous system improvements

Process Analysis & Engineering Support

Review and interpret Piping and Instrumentation Diagrams (P&IDs)
Analyze and document complex Cleaning-in-Place (CIP) and Sterilization-in-Place (SIP) process flows
Collaborate with process engineers and equipment owners to ensure accurate implementation of manufacturing requirements
Support process optimization and manufacturing system enhancements

Documentation & Compliance

Prepare, review, and maintain GMP-compliant documentation, including:
- Electronic Batch Records (eBRs)
- Functional Specifications
- Standard Operating Procedures (SOPs)
- Validation Documentation
- Test Scripts
- Work Instructions
Ensure compliance with quality standards, regulatory requirements, and data integrity principles

Continuous Improvement

Identify opportunities to enhance manufacturing efficiency and system performance
Contribute to automation and digital transformation initiatives
Support operational excellence while maintaining strict compliance and quality standards

Your Profile

Required Qualifications

Bachelor's or Master's degree in Automation Engineering, Process Engineering, Chemical Engineering, Biotechnology, Pharmaceutical Engineering, or a related technical discipline
Hands-on experience with Emerson Syncade MES
Experience developing, configuring, and troubleshooting Electronic Batch Records (eBR)
Solid understanding of GMP-regulated manufacturing environments
Experience with MES implementation and manufacturing operations support
Strong knowledge of P&ID interpretation and CIP/SIP process mapping
Excellent written and verbal communication skills in English

Preferred Qualifications

Experience with Emerson DeltaV
Knowledge of DCS, PCS, or other industrial automation platforms
Experience with validation and qualification activities (IQ/OQ/PQ)
Background within biopharmaceutical, pharmaceutical, or life sciences manufacturing
Additional European language skills are considered an advantage

What You Bring

Strong analytical and problem-solving skills
Structured and organized way of working
Ability to manage multiple priorities in a dynamic project environment
Excellent communication and stakeholder management skills
High attention to detail and commitment to quality and compliance
Self-motivated mindset with the ability to work both independently and collaboratively

Interested?

If you have a passion for manufacturing automation, digitalization, and MES solutions within a regulated environment, we look forward to receiving your application and learning more about your experience with Emerson Syncade and biopharmaceutical manufacturing systems.

Jetzt bewerben

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