Overview
Hybrid
$60 - $70
Accepts corp to corp applications
Contract - W2
Contract - Independent
Skills
FDA
CE Marking
ISO Quality Systems
Medical Device Development
Job Details
Software Project Manager with Medical Device Development exp
Duration: 6-months CTH
Location: Boston, MA (Hybrid)
Interview Mode: Video
Experience Details:
- 5 plus project management leading medical device development.
- Experience with medical device development under FDA Quality Systems Regulations, CE Marking, and ISO Quality Systems
- Technical project management in software product development
Responsibilities/Essential Duties:
- Analyze project risks and identify their impact while developing mitigation strategies, identify and manage critical path, ensure appropriate project level definition across all stake holders and manage the project from concept to commercialization
- Creates and executes project work plans and revises as appropriate to meet changing needs and requirements.
- Manages day-to-day operational aspects of a project and scope. Complies with the Stage Gate Process quality system and helps to enforce standard operating procedures (SOPs). Escalates appropriately when required.
- Mitigates team conflict and communication problems. Escalates appropriately when required. Motivates team to work together in the most efficient manner.
- Leverages project management tools to assist in the development of and adherence to a schedule and reporting status.
- Own and create appropriate levels of governance to ensure alignment and clear objectives
- Accountable for product compliance to design history file, regulatory standards, and QMS procedures
- Keeps track of lessons learned and shares those lessons with team members
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