Data operations manager állások Svájcban (mérnök)

Taking responsibility for regular product care activities within the Squad. Like handling of non-conformity notifications, leading investigations and root cause analysis, coordinating corrective actions in the manufacturing process, implementing changes to the process....

For our partner located in the canton of Bern, GI Life Sciences is looking for a: SENIOR SCIENTIST BIO-/CHEMICAL QUALITY CONTROL Start : Mid-November End : YOUR MISSION : As a SENIOR SCIENTIST IN BIO-/CHEMICAL QUALITY CONTROL, you will play a key role in establishing the BCQC unit within the...

• Provide product care and hardware improvements for existing products through continuous refinement and the introduction of innovative technology solutions
• Coordinate and manage suppliers of third-party electronics manufacturers, ensuring product quality and compliance

Owning the interface with defined SEMI OEMs regarding all commercial and technical aspects of VAT's new gas delivery product portfolio....

• Developing the design of new catheters from conception to complete product.
• Designing products with a focus on efficacy, manufacturability, and operational safety.
• Collaborating with cross-functional team members throughout product development phases to ensure program success.

• Management of Site Safety in conjunction with the Mercury Safety Advisor.
• This will include the setup, management of and closing out of the safety file as part of the Management team.
• Supervise and Inspect work to ensure compliance with standard procedures and electrical assignments.

• Conducting and scheduling internal and external system and process audits (ISO 9001,, and, as well as IATF), including customer audits
• Evaluating and maintaining data for the environmental management system
• Tracking of CIP, measures from audits and their effectiveness

• Management of the Electrical Systems under your control. 
• To support the engineering requirements through managing & liaising with Key Project Stakeholders (Client design team, Main contractor, Suppliers, Sub-contractors, etc). 

• Management of the Mechanical Systems under your control.
• To support the engineering requirements through managing & liaising with Key Project Stakeholders (Client design team, Main contractor, Suppliers, Sub-contractors, etc)

• Configure and equip a designated workshop for end-effector manufacturing and a dry lab for system testing and demonstrations.
• Establish, maintain, and operate ROSI's robotic systems, including clinical-grade and research platforms.

• Build, analyze and interpret FEA models of stirred-milling parts and assemblies in Ansys Mechanical
• Provide proof of stability for static and dynamic loads and complete structural analysis of mill components and special tools

• Coordinate SICPA's IMS activities across more than 20 sites worldwide.
• Maintain and control process mapping and system documentation, ensuring accuracy and compliance with quality standards.

• Act as the primary interface for government and special mission customers, managing all communication, coordination, and reporting.
• Translate customer requirements into clear, actionable work scopes for internal teams.

Prepare, support the creation and review and execute the release of all technical documentation for digital health and software products ensuring compliance with applicable standards and regulatory requirements such as IEC, IEC...

• Lead and develop the company-wide Quality Management System in line with ISO 9001/14001/27001/and relevant industry standards
• Inspire and empower an agile, high-performing quality team and foster a strong “zero-defect” culture across all functions

• Highly skilled in SolidWorks
• Ability to create Technical Assembly and Work Instruction
• Familiarity with PDM/PLM systems for data and revision control
• Experience with Design for Manufacturing (DFM) and Design for Assembly (DFA) principles