Project Manager

vor 2 Monaten

SaintSulpice, Schweiz Tandem Diabetes Care Switzerland Vollzeit

**GROW WITH US**:
Tandem Diabetes Care Switzerland Sàrl, a subsidiary of Tandem Diabetes Care, Inc., is a MedTech start-up located in EPFL’s Innovation Park in Lausanne, Switzerland. Tandem Diabetes Care, Inc., is a global insulin delivery and diabetes technology company based in San Diego, California. Together we are creating new possibilities for people living with diabetes, their loved ones, and the healthcare providers through a positively different experience.

**INNOVATE EVERYDAY**:
Tandem Diabetes Care Switzerland is developing Sigi, a next-generation insulin “patch pump” that will offer additional treatment options for people with diabetes. This pump is based on a patented microfluidics technology developed in-house over the past 6 years. You can find out more about Sigi here.

**A DAY IN THE LIFE**:
Leads cross-functional core teams and manages software and/or system projects through Tandem’s product development process, with the main goal of developing and delivering new medical device products to market.
Acts as the internal liaison between engineering, marketing, manufacturing, and RA/QA for the purpose of establishing and driving the team’s project plan and schedule with clearly defined core team roles and responsibilities, budgeting resources, and reporting on the progress of the projects.
Acts as a key facilitator in Tandem Product Development Process including facilitation of Design Phase Review meetings and progress tracking with the Tandem governance meetings.
The Project Manager is also expected to lead or participate in product development continuous improvement projects led by the PMO.

Working from Tandem Diabetes Care Switzerland’s office onsite in Switzerland, you’ll.
- Provide project management expertise and leadership to a multi-functional core team from Concept through Commercialization following Tandem’s standard process for product development and/or design change.
- Ensure implementation and compliance with Design Control procedures and improvements of systems, procedures, and documentation when appropriate.
- Plan and direct all aspects of software/systems projects.
- Establish project plans and objectives, develop project cost analysis, establish, and manage the project schedule and budget, manage resources, track progress, and provide updates to management.
- Work closely with the Program Management Office, Project Managers, and functional heads to resolve resource allocation issues, conflicts, and priorities and to ensure projects are staffed appropriately, completed on time, and within budget constraints.
- Ensure efficient transfer of product from R&D to manufacturing.
- Lead/participate in process improvement initiatives related to product development, resource management and allocation, design controls, and other areas that impact cycle time, efficiencies, and compliance in medical device product development.
- Communicate and present regular and timely project status updates to various levels of the organization.
- Ensure compliance with company policies, including Privacy/HIPAA, and other legal and regulatory requirements.

**YOU'RE AWESOME AT**:

- Ability to work in matrixed environment, establishing a sphere of influence with both the functional and vertical organizations.
- Ability to drive change through implementation of best practices in project teams.
- Ability to communicate and influence up in order to manage project scope and resources.
- Ability to keep project teams focused, motivated, creatively work to keep the projects on schedule.
- Proficient in the use of Project Management Tools for planning, work breakdown, scheduling, task estimation, and collaboration.
- Ability to assess a problem quickly and determine to what level it should be elevated, directing staff/customers to the correct person(s).
- Excellent advocacy and persuasive skills.
- Ability to organize and prioritize workflow and to meet established timeframes.
- Ability to work in an agile, fast-paced environment.
- Ability to maintain updated knowledge of products, procedures and of changes within the medical device industry.
- Ability to provide feedback and suggestions for improvement on the Product Development Process.
- Advanced Microsoft Office skills with Excel, PowerPoint, and MS Project.
- Fluency in English required, fluency in French preferred.

**YOU'LL NEED**:

- Master’s degree in Engineering or a related field
- Certificate in Project Management (PMP or equivalent)
- + 5 years’ experience managing projects; Medical device industry, FDA-regulated, and ISO 14971 certified industry preferred.
- Experience in managing projects from inception to post-market sustaining using a phase-gate/agile methodology.
- Experience managing multiple projects at a time.
- Strong understanding of engineering principles, theories, and concepts
- Knowledge of agile/scrum development methodology.

**WHAT’S IN IT FOR YOU?**

In addition to innovative technology, we have a cultu

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