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offre d'emploi

cv

    publié le 23. avril 2026

    référence
    25038
    contact

    n'hésite pas à nous contacter pour toute question.

    R

    Richa Bali

    +41 58 201 56 70

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    offre d'emploi

    Looking for a Rust expert (2+ years) to drive the development of high-quality medical device software. You bring strong problem-solving skills, a collaborative mindset, and the ability to lead by example in a diverse, cross-functional environment.

    ...

    General Information:

    • Planned duration: 31.12.26
    • Extension (in case of limitation): yes
    • Workload: 80-100%
    • Home Office: 2 days onsite required
    • Team: 10-12
    • Working hours: Standard


    Tasks & Responsibilities:

    • Develop and maintain software solutions by applying in-depth technical knowledge and problem-solving skills, while ensuring compliance with regulatory standards for medical software
    • Ensure the timely delivery of high-quality software for medical devices that meets both the company's standards and customer needs, influencing the success of the team and broader project outcomes
    • Communicate complex technical concepts effectively, fostering an environment of collaboration and continuous learning within and across diverse and intercultural teams
    • Empower your team members to take ownership of their work and leading by example to foster teamwork and mentorship
     

    Must Haves:

    • Bachelor’s degree or equivalent practical experience in a specialized field related to software development or engineering 
    • Several years of proven experience in software development, with a demonstrated passion and hands-on professional experience working with Rust for at least two years incl. a solid understanding of Rust's core concepts (ownership, borrowing, and lifetimes), experience with asynchronous programming in Rust (e.g., using async/await) and familiarity with common Rust libraries and frameworks (e.g., tokio, actix-web, rocket, serde, sqlx)
    • Hands-on experience with modern system architectures like event-driven architecture and DDD, quality-driven practices such as TDD and BDD, or containerization technologies like Kubernetes is a plus
    • Capable of solving complex issues creatively and effectively, using a multi-faceted approach based on thorough analysis to resolve complex technical challenges 
    • Excellent communication skills with the ability to foster an inclusive and diverse environment as well as collaborate effectively within and across teams 
    • Motivation to make an impact to your fellow team members, our company, our customers and our patients
    • Leads by example to foster cross-functional value delivery and to establish a psychologically safe working environment and empowers its own team and holds people accountable by creating conditions for ownership
    • Experiences as a Technical Lead within a team is a plus
    • Certified ISAQB or equivalent is a plus
    • English fluency is a MUST, German is a plus


    We thank you for your application!

    montrer plus

    Looking for a Rust expert (2+ years) to drive the development of high-quality medical device software. You bring strong problem-solving skills, a collaborative mindset, and the ability to lead by example in a diverse, cross-functional environment.


    General Information:

    • Planned duration: 31.12.26
    • Extension (in case of limitation): yes
    • Workload: 80-100%
    • Home Office: 2 days onsite required
    • Team: 10-12
    • Working hours: Standard

    ...

    Tasks & Responsibilities:

    • Develop and maintain software solutions by applying in-depth technical knowledge and problem-solving skills, while ensuring compliance with regulatory standards for medical software
    • Ensure the timely delivery of high-quality software for medical devices that meets both the company's standards and customer needs, influencing the success of the team and broader project outcomes
    • Communicate complex technical concepts effectively, fostering an environment of collaboration and continuous learning within and across diverse and intercultural teams
    • Empower your team members to take ownership of their work and leading by example to foster teamwork and mentorship
     

    Must Haves:

    • Bachelor’s degree or equivalent practical experience in a specialized field related to software development or engineering 
    • Several years of proven experience in software development, with a demonstrated passion and hands-on professional experience working with Rust for at least two years incl. a solid understanding of Rust's core concepts (ownership, borrowing, and lifetimes), experience with asynchronous programming in Rust (e.g., using async/await) and familiarity with common Rust libraries and frameworks (e.g., tokio, actix-web, rocket, serde, sqlx)
    • Hands-on experience with modern system architectures like event-driven architecture and DDD, quality-driven practices such as TDD and BDD, or containerization technologies like Kubernetes is a plus
    • Capable of solving complex issues creatively and effectively, using a multi-faceted approach based on thorough analysis to resolve complex technical challenges 
    • Excellent communication skills with the ability to foster an inclusive and diverse environment as well as collaborate effectively within and across teams 
    • Motivation to make an impact to your fellow team members, our company, our customers and our patients
    • Leads by example to foster cross-functional value delivery and to establish a psychologically safe working environment and empowers its own team and holds people accountable by creating conditions for ownership
    • Experiences as a Technical Lead within a team is a plus
    • Certified ISAQB or equivalent is a plus
    • English fluency is a MUST, German is a plus


    We thank you for your application!

    montrer plus
      contact

      n'hésite pas à nous contacter pour toute question.

      R

      Richa Bali

      +41 58 201 56 70
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        published on 12 mai 2026
      • CSV Experte (Distributed Control System)

        • Bâle, Bâle-Ville
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        <p>For one of our clients, a global pioneer in pharmaceuticals, we are currently looking for a CSV Expert (Synthetic Molecule Facility).</p><p>General Information:</p><ul><li>Start Date: ASAP</li><li>Latest possible start date: 01.08.2026</li><li>Planned Employment Duration: 12 months with the possibility of extension</li><li>Workplace: Basel</li><li>Home Office: No</li><li>Workload: 40-60%</li><li>Team: 10 people</li><li>Traveling: No</li><li>Department: Basel Site Services Chapter G10 (EFHCAH)</li><li>Working Hours: Standard</li></ul><p>About the job:</p><p>The "Synthetic Molecule Clinical and Launch Facility" (SMF) project involves modernizing the existing development and commercial launch production for drug-substance small molecules. The production control systems planned within the Synthetic Molecules Facility (SMF) project are to be qualified/validated according to CSV.</p><p>The ideal candidate</p><p>Possess extensive experience as a CSV expert with in-depth knowledge of process control systems (PCS) in a pharmaceutical GMP environment. Demonstrable experience in creating validation-compliant URS, specifications (GxP/CSV), and test plans, as well as experience in using electronic documentation and workflow tools (eVAL) for validation, is essential.</p><p>Tasks & Responsibilities:</p><ul><li>CSV Documentation: Leading the creation of validation-compliant User Requirements Specifications (URS) and Functional Specifications (FS) in accordance with GxP/CSV guidelines.</li><li>Solution's & Compliance: Ensuring that the implementation of validation activities for the process control system meets CSV requirements.</li><li>Execution Planning: Creating a roadmap and a detailed schedule for execution and validation.</li><li>Monitoring of execution: Ensuring that the requirements are implemented to the required quality, within the specified timelines and in compliance with CSV standards.</li><li>Interface: Act as coordinator between Technical Compliance and the implementation teams.</li></ul><p>Must-haves:</p><ul><li>Education/degree ideally as an automation engineer or comparable qualification</li><li>At least 10 years of experience in CSV (Computerized System Validation) in a pharmaceutical GMP environment</li><li>Demonstrable experience with process control systems (PCS) or similar automation systems in production</li><li>Demonstrable experience in creating validation-compliant URS and specifications (GxP / CSV)</li><li>Very good IT/tool skills, especially regarding documentation and workflow tools for validation</li><li>English (good knowledge)</li></ul><p>Nice-to-haves:</p><ul><li>Experience as a project manager of digitalization projects in a pharmaceutical GMP environment.</li></ul><p>Sounds interesting? Apply now – we’re looking forward to receiving your applications!</p><p>Application Submission Deadline: 21.05.2026</p>
        published on 12 mai 2026
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