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Title: Lead Validation Consultant
Location: Marlborough, MA (Day 1 Onsite)
Duration: 8+ Months (Possibilities for Extension)

Job Description:

Required Qualifications:
· 10+ years of experience with Information technology.
· 6+ years of experience with the medical device industry.
· Experience working with QT, C++ and Linux.
· Experience working with Rapid Prototype.
· Experience working with OPENGL.
· Experience working on software design verification of medical devices
· Experience working on UI development and testing.
· Candidates must be located within commuting distance of Marlborough, MA or be willing to relocate to the area.
· BS or MS Degree in Computer Science, Computer Engineering, Software Engineering, or related field.

Responsibilities include:
· Designs, develops, debugs, modifies, and reviews regulated software tools used to support the software verification process.
· Tracks software development and testing effort by creating and maintaining records in the approved tracking management tool.
· Solves engineering problems by analyzing the situation and recommending corrective or alternative actions.
· Uses version management tools to manage test assets in a concurrent design environment.
· Collaborates with requirements and development teams to coordinate resolution of software errors.
· Coordinate and collaborate with global team members.
· Participate in the Agile software development process and work towards achieving individual and team goals.
Continuously improves process and work methodologies by interfacing with peers/cross-functional groups and analyzing activities to improve workflow and work processes.

Preferred Qualifications:
· Experience leading teams using Agile or Kanban methodologies.
· Capacity to multi-task several testing activities concurrently