Job Description
Join to apply for the Principal Engineer, DDS Devices role at Johnson & Johnson Innovative Medicine.
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter, less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
All Job Posting Locations:
Schaffhausen, Switzerland
Job Function
* R&D Product Development
* Biomedical Engineering
* Scientific/Technology
Responsibilities
* Guide project team activities to meet project and business with specific focus on assembly process development and development of the control strategy
* Drive team accountability for process improvement and implementation, helping to communicate the importance of process development throughout the organization.
* Demonstrate business acumen, project management, communication, process management and team performance management; ask the right questions to understand business impact and risks
* Make the complex simple and represent a true enterprise view when communicating opportunities and plans to the team and organization
* Lead team through options analysis and drive multi-functional recommendations
* Evaluate different assembly technologies with a multitude of device and primary container platforms.
* Use scientific and engineering judgment, generate data where needed. Coordinate the assembly process development within the framework set by the Quality Management System and the Regulations and align dates and expectations with key stakeholders.
* Understand technological advancements, environmental changes, key competitor’s offerings; and provide analysis on technological feasibility, I/P landscape, risk assessment, and sales and market considerations
* Strong knowledge of FDA Design Controls/ISO13485 and medical device product development experience required. Strong knowledge and demonstrated successes in the development of drug-device assembly processes.
Facilitation & Risk Management
* Excel at enterprise leadership and facilitation, collaboration, attention to detail Identify and recommend the best enterprise business proposition
* Engage teams in healthy debate, and deliver solutions
* Scope definitions and control: stakeholder alignment, project planning, resource and risk management, project leadership, team development and communication
* Lead teams in use of ongoing risk management & communication tools
* Proactively identify and call out risks and issues to relevant stakeholders; lead development and delivery of tactical and achievable mitigation and contingency planning
Project Execution
* Develop a project plan, and then deliver the project plan to achieve business results
* Provide demonstrated proficiency in MS Project.
* Deliver transparent, timely and effective verbal and written communication to teams, stakeholders and appropriate levels of the organization
* Lead \
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