Join a Leading Global Biotechnology Company
We are excited to present an opportunity with a prominent biotechnology organization based in the greater Lucerne area. This company is dedicated to being the world’s most trusted supplier of biopharmaceuticals, operating a robust global manufacturing network that ensures high-quality medicines are delivered to patients safely and on time.
About the Role
The position focuses on the implementation, configuration, validation, and maintenance of Manufacturing Execution System (MES) solutions based on Werum PAS-X. Here, you will make valuable contributions to the development and maintenance of electronic manufacturing recipes, offering crucial technical support to manufacturing operations in a collaborative, cross-functional environment.
Your Responsibilities
- Foster diversity and inclusion, building effective working relationships within a cross-functional team across various cultures and backgrounds.
- Configure, build, and maintain MES (PAS-X) GMBRs and recipes according to established Design Standards and site requirements.
- Execute testing, verification, and documentation activities in support of GMBR releases and system changes.
- Provide daily MES (PAS-X) support to manufacturing operations, including troubleshooting of recipe execution and electronic batch record (EBR) issues.
- Assist in investigations and deviations by identifying and resolving MES and automation-related problems.
- Prepare and execute Change Controls, ensuring timely compliance with quality standards.
- Support the administration and maintenance of MES systems to ensure automation systems remain validated.
- Facilitate the integration of PAS-X with site automation layers and SAP, guided by senior engineers.
- Contribute to continuous improvement of business process flows and technical MES workflows.
- Support the development and updating of automation SOPs and training packages, conducting MES training for end users.
- Ensure all documentation aligns with SDLC requirements.
- Assist in Technical Transfers of process technologies from early-stage pipeline facilities from an MES perspective.
- Perform any additional duties as 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, specifically PAS-X experience as a strong advantage.
- Minimum of 2 years of experience in Automation or Engineering functions within the Biologics, Food, Medical Devices, or Pharmaceutical industries.
- Familiarity with computer validation/SDLC requirements and change control procedures (e.g., GAMP 5).
- Hands-on experience in MES GMBR configuration, testing, and execution support, with PAS-X system expertise being an advantage.
- Understanding of MES integration concepts, including interfaces to automation and SAP systems, is beneficial.
- Ability to manage multiple priorities and recognize when to escalate issues for resolution.
- Strong problem-solving and troubleshooting skills, with a detail-oriented approach.
- Effective oral and written communication skills in English (B2/C1).
- Exposure to commissioning and validation, along with experience in test protocol execution, is an added advantage.
Additional Information
- Location: Schachen
- Contract Duration: 12-month contract position, starting in October 2026, with potential for extension.
- Type of Employment: Temporary staffing