Description

You will lead the complete overhaul of maintenance documentation to ensure regulatory compliance, coherence, and accessibility. You will interface with maintenance and quality to structure, optimize, and sustain the standards. Our client is an innovative Swiss company active in high-value-added medical technologies that operates in a demanding regulated environment, combining excellence and a culture of continuous improvement.Missions:- Analyze and review the entire maintenance documentation to update SOPs, SM X according to internal standards and re-verify document compliance (ISO, 21 CFR 820 Subpart G).- Ensure the coherence of versioning and cross-references by removing links between parent and child documents.- Identify obsolete documents and establish a removal plan.- Harmonize documentation with maintenance teams.- Optimize existing processes based on SOPs by improving the accessibility and usability of documents.- Ensure compliance with archiving rules and management of documented information in a regulatory environment.- Strong knowledge of quality and regulatory requirements processes in a medical environment.- Good mastery of MS Office 365 and Visio.- Ability to analyze, structure, and standardize content methodically, rigorously, and with a sharp focus on document quality.- Excellent communication skills and ease of interaction with maintenance, quality, and teams.- Fluency in spoken and written French and a professional level of English.Conditions and Benefits:- A temporary assignment in a regulated high-tech environment with cross-functional interactions with expert teams.- Compensation in line with the Swiss market. jided02361aen jit0206aen jpiy26aen