Pożądane doświadczenie zawodowe
Education: BS in Engineering. MS in Engineering or equivalent experience. PhD or MBA is a plus.
10+ years experience in the engineering/development of complex integrated systems comprisedof electromechanical, fluidics and/or assay/chemistry subsystems. Ideally in the life sciences /diagnostics industry or equivalent experience in other industries. Should have full product development cycle experience with demonstrated commercial success of the product in thefield.
5+ years experience with hands on laboratory testing execution covering a large variety of/engineering tools/equipment, test methods/design of experiment and outcomes at various stage of product maturity.
3 years of demonstrated functional/project management experience of managing and growing successful engineering teams.
Experience working in a regulated industry, ideally with IVD experience, QSR/ISO regulations(e.g., ISO 13485, IEC 62304) & standards and risk management (ISO14971).
Excellent problem-solving, organizational, analytical, and critical thinking skills including high discretion/judgment in decision making. Ability to foresee, plan and manage risks within currentproject and/or technology
Ability to interact professionally with all organizational levels. Ability to work and excel within a fast paced, dynamic, evolving and changing work environment.
DFSS Green Belt or Black Belt certification or other training in Design for Excellence principles is desirable.
Familiarity with software development life cycle (SDLC) processes, agile methodologies, and continuous integration/continuous deployment (CI/CD) practices.
Proficiency with Python, or Matlab preferred for scripting or data science application
Establish, maintain, and execute on the system design Integration/Verification plan for a new medical diagnostic device and its subsystems (Test Cycles definition, Test Articles configurations,Design Requirements prioritization, Integration/Verification strategies),
Develop just in time test protocols to support a traceable continuous integration design methodology (Test Method library, Sample Size determination, Risk Management mitigations),
Lead test execution throughout the entire development effort across the medical diagnostic device and its subsystems (test Personnel capability & capacity, test Equipment development & qualification, test Vendors partnerships),
Report test outcome with traceable objective evidence to support unbiased technical andproject decisions (Defects report, Statistical significance, Technical/Design reviews, RegulatoryAgency/Notified Bodies submissions),
Ensure objective evidence traceability throughout the entire product development lifecycle (Raw data & records retention, Quick access to multiple layers of information, Design HistoryFile).
Champion the adoption and execution of a Shift left strategy through System Design
Integration/Verification process improvements and state-of-the-art best practices (Design for Six Sigma, Continuous Integration tools, LEAN management, Design Control),
Leverage a global talent pool (France, Switzerland, USA) to optimize project testing activities quality, cost & duration based on Design Modules reuse.
Provide technical leadership and knowledge of engineering principles and their application to developing cost- effective, reliable, and high-quality test methods that include elements of microfluidics, optics, thermal transfer, nucleic acid amplification, and robotics.
Eventually be able to lead a systems Integration/Verification team and implement functional management processes and tools to monitor progress of engineering deliverables across the portfolio.