Formateur Outils Bureautiques H/F

We are recruiting a 3D Industrial Computer Graphics Project Manager on a permanent contract to join our center of expertise on a large-scale, long-term project to expand our partner's activities.

As a 3D Computer Graphics Project Manager, the objective will be to collaborate with the development team and graphics team to produce 3D and 2D assets, images, video animations, or real-time 3D applications related to the company's industrial activity. Main elements:

• Optimization of 3D elements from Computer-Aided Design (Blender and Pixyz).
• Texturing (Substance, Blender, Unity).
• Integration and optimization of real-time 3D scenes (Unity).
• Knowledge of the production workflow of a real-time 3D project.
• Production of pre-calculated 3D images and videos (Blender).
• Creation of 2D elements (textures, UI) (Adobe Suite).
• Technological, artistic and business intelligence.

We are recruiting a Watchmaking Product Industrialization Project Manager on a permanent contract to join our Industrial Expertise division as part of a large-scale, long-term project to expand the activities of our partner in Geneva.

As a Watchmaking Product Industrialization Project Manager, your responsibilities will include :

• Plan and lead technical convergence reviews, including process plans, controls and capabilities.
• Develop and industrialize ranges and bills of materials for new products.
• Manage activity planning and risk management.
• Unite the resources involved.
• Manage and implement product and process evolutions, adapting the governance of series during their life cycle.
• Capitalize on best practices and contribute to the development of reference systems.
• Manage the model plan approach in line with industrial tool capacities.

Job Description:

• Contribute to Life Science projects for Antaes Asia clients.
• Work with cross functional team in providing Quality oversight in computerized system life cycle procedure and ensure compliance to GXP standards and company policies and procedures.
• Provide guidance and support to establish systems for ensuring Data integrity, compliance to CSV Plan and 21CFR Part 11.
• Act as one of the key focal points for CSV topics such as deviations, change management, investigations, CAPA identification and closure, and as a Subject Matter Expert.
• Generate, review and execute protocols / test case for initial validation programs related to GXP Computer systems. -e.g. Qualifications protocols - Software qualification, Input/Output loop verification, hardware qualification.
• Review and approve qualification documentations like URS, SLIA (system level impact assessment)/ CLIA (component level impact assessment), SRA (System Risk Assessment), DIRA/ DSA (Data security, audit trail review), DQ, SIOQ, HIOQ, FAT, FATSR, Traceability Matrix etc.
• Ensure adherence to CSV master plans and execution plans for GXP computer systems like DCS, PLC, BMS, MES, eBR, Lab Information systems, Environmental monitoring systems and other Business IT systems like Maximo, Network and ERP systems that are part of the GMP envelope.
• Any other tasks assigned.
• Contribute to the promotion of Antaes services on top of assistance provided to clients.

Job Description:

• Contribute to Life Science projects for Antaes Asia clients
• Develop and execute CQV documentation including commissioning protocols, FAT/SAT reports, IQ/OQ/PQ protocols, summary reports, and traceability matrices.
• End-to-end support for the CQV lifecycle for process, utility, and support systems—e.g., bioreactors, chromatography skids, filtration units, CIP/SIP, WFI, HVAC, autoclaves, and clean utilities.
• Participate in design reviews (URS, SDS, P&ID walkdowns) to ensure CQV considerations are integrated during project design and construction.
• Manage the execution of commissioning and qualification activities in line with project schedules, safety standards, and GMP compliance.
• Support automation qualification (DeltaV, PLC, SCADA) and ensure integration with process control systems.
• Review vendor documentation and coordinate FAT and SAT with suppliers and engineering teams.
• Troubleshoot and resolve technical issues encountered during CQV execution.
• Ensure all CQV deliverables meet internal Quality and Validation standards, and align with the site Validation Master Plan (VMP).
• Support the handover of qualified systems to Manufacturing and Maintenance teams, including training and documentation.
• Collaborate closely with cross-functional teams including Engineering, QA Validation, Manufacturing, and Automation.
• Contribute to the promotion of Antaes services on top of assistance provided to clients.