Project Manager II

Our client, a small medical device development company, has engaged GForce Life Sciences to provide a Project Manager II. This position will report to aDirector of Engineering. This individual will be responsible for both strong technical skills and driving project timelines.

In addition, this person serves as the primary client-facing project leader responsible for coordination of laboratory testing activity, driving execution across engineering and quality teams. They need to ensure alignment between client expectations and internal deliverables. Programs may include design verification, method validation, complaints testing, engineering investigations and container closure integrity testing (CCIT) for devices such as autoinjectors, syringes, inhalers, pumps, wearable injectors and vial access systems.

Experience supporting Design History File (DHF) activities and broader medical device development processes is preferred.

• Manage a portfolio of medical device and drug-device combination product testing projects, ensuring delivery meets agreed timelines, budgets, and client requirements.
• Align engineering, laboratory, quality, and project management resources to keep testing programs moving efficiently.
• Facilitate project check-ins and issue-resolution discussions to address technical challenges, operational barriers, and scheduling conflicts.
• Partner with on-site teams to balance testing priorities, equipment access, and staffing needs across active client engagements.
• Communicate with clients and technical colleagues about testing approaches, troubleshooting, investigations, and verification plans.
• Provide technical leadership on selected assignments, including test protocols, analysis of results, engineering investigations, and supporting documentation.
• Help organize laboratory workloads and allocate resources to support timely delivery and responsive client service.
• Track project status, emerging risks, capacity limitations, and changing client priorities to anticipate and address potential delays.
• Foster teamwork, ownership, technical rigor, and timely execution, with an emphasis on accurate, complete work from the outset.

• Bachelor’s degree in Engineering, Biomedical Engineering, Mechanical Engineering, Life Sciences, or related technical field required.
• 5+ Years of experience in combination product and/or medical device development, testing or engineering.
• Strong understanding of laboratory operations, testing coordination and management of priorities across multiple active testing programs
• Working knowledge of applicable regulatory and quality system requirements including cGMP, cGLP, cGDP, ISO standards
• Proficiency in MS Office Tools such as Excel, Word, PowerPoint, Teams and Project Management tracking tools.

• PMP certification

• Permanent Role
• Onsite 4-5 days a week in Northbrook, IL
• Benefits included (Medical, Dental, Vision, 401k)