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German speaker Lead Application Development (Medical Dev)

Location: Switzerland
Sector: Other
Job Type: contract
Salary: Negotiable
Reference: BBBH126804

German speaker Lead Application Development (Medical Dev)

Experis recognises you are more than just a CV. As part of the ManpowerGroup we have access to a huge network of opportunities, and we'll connect you to the roles that will accelerate your career.

My client is one of the fastest growing pharma businesses in Switzerland and is looking for a Lead Application Developer for its office in Basel. My client is requesting a highly skilled individual who specializes in software and system architectures and can meet target deadlines.

The successful candidate is a recognized expert for development and maintenance of safety critical mobile and/or web applications and will take over the technical leadership for the software development part for projects within the Packaging & Device Development Team. The role includes early phase development activities, the management and monitoring of software development and the commercialization and maintenance of overall life cycle management as legal manufacturer. In addition to outstanding project management and interpersonal skills, a strong background in software development and lifecycle management, as well as the use and implementation of platform technologies, is crucial for this role.

Tasks and responsibilities:
* Technical leadership for the software development of mobile and/or web applications classified as SaMD
* Providing software/systems life cycle expertise within a broader cross‐functional drug product development team,
* Supporting the standardization of the entire SaMD life cycle management process in order to utilize cross‐product synergies,
* Leading the collaboration with external development partners:
o Support supplier selection, auditing and approval,
o Elaboration of development plans and contracts for upcoming projects,
o Monitor, support and challenge technical development and deliverables as well as change, test and release strategies,
o Support the deployment and implementation of a sustainable Product Life Cycle process in close collaboration with external and internal partners and stakeholders,
* Leading and/or supporting cross functional project teams during development, review and submission of regulatory dossiers,


* MSc/MA in computer science or relevant field and excellent understanding of the current Agile development methods and technologies,
* Experience in project / program management of complex projects,
* Autonomous and independent working style with at least 7 years of experience as technical, project management of projects with safety critical applications in a regulated environment,
* Team player who works efficiently in interdisciplinary teams,
* Experience in designing innovative software and systems architectures,
* Analytical thinking and problem‐solving capability,
* Excellent understanding of software design and programming principles as well as in overall verification strategies, including test set‐up and test automation
* Good communication and conflict management skills,
* Considerable experience of managing external suppliers,
* General understanding of Human Factors Engineering, risk management and clinical studies processes and requirements
* Understanding of medical device regulations (FDA 21CFR 820, FDA 21CFR Part 4, EU Medical Device Directive, EU Medical Device Regulation), including those related to medical software (IEC 62304)
* Development and writing of technical documentation of drug/device combination products and medical devices, including the design control process and other applicable regulatory, QA and GMP aspects,
* Understanding of pharmaceutical development in general
* Proficiency in German

Start date: October 15th 2020

Duration: 1 year

Location: on-site in Basel, Switzerland

Interested in this opportunity? Kindly send us your CV today through the link in the advert. However, should you have any questions please contact Virginia Belli on +41 61 282 22 10

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