About The Position

Co-op – Design Release Engineer - Cambridge, MA - June- December 2025 Are you interested in an Internship opportunity with Philips? We welcome individuals who are currently pursuing an undergraduate (BS) and/or graduate (MS) degree to participate in paid intern opportunities. Through this role you will gain meaningful, hands-on experience working for a HealthTech company. Your role: You are responsible for contributing to the team’s execution of software design changes and associated design control deliverables. Execute project tasks and deliverables based on interdependences and project requirements. Collaborate with the team to achieve continuous value delivery by identifying solutions to decrease process time while maintaining value and quality. Identify areas for process improvement and opportunities to achieve Continuous Value Delivery. Collaborate cross-functionally with team members, senior leaders, and stakeholders within the businesses to accomplish project goals and objectives. Coordinate with other project leaders and managers leading program project. Adhere to all QMS procedures and Q&R standards to ensure patient safety and quality are prioritized.

Requirements

  • Must be currently enrolled in a Bachelor’s or Master’s degree program majoring in Computer Science or Biomedical Engineering
  • You’ve acquired experience in cross-functional teams.
  • Knowledgeable about regulated product development/design change environments, with FDA regulated medical device experience preferred.
  • You have experience in implementing new tools/processes, process/continuous improvement, and change management.
  • Highly skilled at negotiating and influencing group dynamics.
  • People focused, collaborative, team player, with a drive for results.
  • Skills include strong team leadership and ability to build, leverage partnerships with project’s stakeholders (internal and external), demonstrating initiative, tenacity and resilience to build effective working relationships.
  • Growth Mindset
  • Excellent communication skills and a customer centric attitude
  • You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position.
  • US work authorization is a precondition of employment.
  • For this position, you must reside in or within commuting distance the job posting location.

Nice To Haves

  • Knowledgeable about regulated product development/design change environments, with FDA regulated medical device experience preferred.

Responsibilities

  • contributing to the team’s execution of software design changes and associated design control deliverables
  • Execute project tasks and deliverables based on interdependences and project requirements
  • Collaborate with the team to achieve continuous value delivery by identifying solutions to decrease process time while maintaining value and quality
  • Identify areas for process improvement and opportunities to achieve Continuous Value Delivery
  • Collaborate cross-functionally with team members, senior leaders, and stakeholders within the businesses to accomplish project goals and objectives
  • Coordinate with other project leaders and managers leading program project
  • Adhere to all QMS procedures and Q&R standards to ensure patient safety and quality are prioritized.
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