Joint Skills in QA and IT Required for French Speaking Role
* A Global Leader in Biopharmaceutical Innovation Seeks a Dedicated Professional
* Immediate Start | Initial Contract: 6 Months (Extension Highly Probable Until End of 2025)
* As a QA IT MES Specialist, You Will Be at the Forefront of Ensuring Excellence and Compliance During the Implementation of an Electronic Batch Record System.
Key Responsibilities:
* Represent Quality in Site and Global Project Teams, Providing Oversight and Expertise on CSV and Validation Activities.
* Ensure All Quality Aspects of the Project Comply with Global Policies, SOPs, and GMP Regulations.
* Review and Approve Key Documentation, Including Risk Assessments, Validation Protocols, and Configuration Specifications.
* Collaborate with Project Teams to Address Quality Issues, Organize QA Activities, and Promote Compliance with Data Integrity Standards.
* Act as a Key QA Liaison, Ensuring Seamless Communication Among Stakeholders and Supporting an Agile Validation Approach.
Requirements:
* Proven Experience in Computerized System Validation (CSV) and a Strong Understanding of cGxPs and Industry Standards.
* Fluency in English and French Is Essential.
* Exceptional Communication and Organizational Skills to Collaborate Across Diverse Teams.
* A Proactive Mindset with Flexibility and Dedication to Meet Project Timelines.
* Residency or Work Permit in Switzerland Is Mandatory (Cross-Border Workers Welcome).
Benefits:
* Collaborate on Cutting-Edge Projects That Shape the Future of Healthcare.
* Work in a State-of-the-Art Facility Overlooking the Beautiful Lake of Neuchatel.