Senior Product Development - Medical devices - Canton of Vaud (BBBH366324) Vaud, Suisse
Senior Product Development
Medical Devices
6 months
Canton of Vaud
Lead product development projects ensuring consistency with corporate strategy, company policies, and regulations. Ensure product performance to customer/functional specifications is in balance with deadlines and budgets. This includes identifying resources and coordinating the efforts of cross-functional project team members to deliver projects according to plan.
Your responsibilities:
Lead product development projects/programs:
- Conduct detailed project planning
- Drive and communicate project execution with detailed timelines and action items
- Provide project updates to project and senior leadership team on an ongoing basis
- Identify risks/roadblocks, provide options to mitigate issues and enlist management support to resolve issues
- Identify project resource needs and manage allocation
- Manage approved project budget
- Collaborate cross-functionally ensuring common focus and understanding of project goals across all functional representatives
- Motivate team members, resolve conflict and facilitate timely decision making
- Lead design reviews and utilize analytical skills to drive technical decision making
Your profile:
- Bachelor of Science Engineering degree (i.e. Mechanical, Chemical, Biomedical, Physics)
- 5+ years work experience leading product development projects
- 3+ years technical experience in one or more areas of development of embedded software, custom electronics, custom mechanical systems and/or consumables, or verification.
- Proficient with project management software
- Proven track record of successfully managing large scale projects
- Strong written and verbal communication skills and interpersonal skills to effectively translate ideas, concepts and information
- Ability to work with different internal and external customers in a professional manner
- Proven experience to work cross-functionally across an organization, at all levels of the organization
- Working knowledge and experience with quality systems regulations and guidelines, ISO, cGMP, Medical Device Directive (MDD), Canadian Medical Device regulations, Japanese PAL and FDA regulatory requirements
- Ability to travel both domestically and internationally
Preferred
- Certification in project management or equivalent
- Advance degree in business or technology
- Experience leading new product development projects/programs
- Experience leading catheter/consumable projects
Other
- Travel requirements are expected to be less than 20%.
Votre contact Kelly
Ana Nunes
Consultant Professional Staffing Life Science
Kelly Scientific Geneva