MES Engineer / MES Engineeress

Job Opportunity: MES Engineer (m/f/d)

We are currently seeking a motivated MES Engineer (m/f/d) for one of our clients, a leading global biotechnology company located in the greater Lucerne area. The selected individual will join the Manufacturing & Supply Division in Schachen, which is dedicated to being the world's most trusted supplier of biopharmaceuticals. This division operates a robust global manufacturing network that ensures high-quality medicines are delivered to patients worldwide, safely and on time.

The Schachen site boasts a diverse team comprising highly skilled scientists, engineers, technicians, and process specialists from over 15 nationalities. The facility plays a critical role in accelerating the development and delivery of innovative medicines while upholding the highest standards of quality, compliance, and operational excellence.

About the Role

As an MES Engineer, you will support the implementation, configuration, validation, and maintenance of Manufacturing Execution System (MES) solutions based on Werum PAS-X. Your contributions will include the development and maintenance of electronic manufacturing recipes and design standards while providing technical support to manufacturing operations in a collaborative, cross-functional setting.

In this role, you will serve as a crucial link between early-stage development and commercial manufacturing, driving innovation, digitalization, and continuous improvement across manufacturing processes. You will collaborate closely with senior MES specialists and the Process Automation MES Lead to simplify, standardize, and optimize MES solutions in support of business and production objectives.

Your Responsibilities

• Inspire Diversity and Inclusion by building effective working relationships within a cross-functional team across various cultures and backgrounds.
• Configure, build, and maintain MES (PAS-X) GMBRs and recipes in accordance with established Design Standards and site requirements.
• Execute tests, verify, and document activities in support of GMBR releases and system changes.
• Provide day-to-day MES (PAS-X) support to manufacturing operations, troubleshooting recipe execution and electronic batch record (EBR) issues.
• Assist with investigations and deviations by identifying and resolving MES and automation-related problems.
• Prepare and execute Change Controls under guidance, ensuring compliance with quality standards.
• Support MES administration and maintenance activities to ensure automation systems remain validated.
• Facilitate the integration of PAS-X with the site's automation layer (e.g., DeltaV Level 2 batch integration) and with SAP (COMET/iMES) under the direction of senior engineers.
• Contribute to the continuous improvement of business process flows and technical MES workflows.
• Assist in the development and updating of automation SOPs, training packages, and deliver MES training to end users.
• Ensure all documentation complies with SDLC requirements.
• Support Tech Transfer of process technologies from early-stage pipeline facilities from an MES perspective.
• Perform any other duties assigned by the Process Automation MES Lead.

Your Profile

• Bachelor’s degree in a Life Science discipline or equivalent practical experience with at least 2-3 years in the MES area; PAS-X system experience is a strong advantage.
• At least 2 years of experience in Automation or Engineering within the Biologics, Food, Medical Devices, or Pharmaceutical Industries.
• Working knowledge of computer validation/SDLC requirements and change control procedures (e.g., GAMP 5).
• Hands-on experience in MES GMBR configuration, testing, and support; PAS-X system experience is preferred.
• Awareness of MES integration concepts, including MES-to-automation (e.g., DeltaV) and MES-to-SAP interfaces, is beneficial.
• Ability to manage multiple priorities and know when to escalate for resolution.
• Strong problem-solving and troubleshooting skills, with a hands-on, detail-oriented mindset.
• Effective oral and written communication skills in English (B2/C1).
• Exposure to commissioning and validation, including test protocol execution (e.g., Kneat eVal), is a plus.

Additional Information

• Location: Schachen
• Contract duration: This is a 12-month contract position planned to start in October 2026, with the possibility of extension.
• Type of employment: Temporary staffing

Apply online using the form below. Only applications matching the job profile will be considered.