Sr. Project Manager

Cirtec Medical; Enfield (CT); On-site; USD 115,000 - 135,000; Full time

Job summary

Cirtec Medical is seeking a Sr. Project Manager to lead and coordinate development projects and manufacturing transfers for complex medical devices. You will manage end‑to‑end program lifecycles, collaborate with engineering, quality and operations, and communicate status to leadership and customers.

The role requires a BS in engineering, at least 5 years in medical device PM, and strong ISO 13485/FDA knowledge. Travel may be required. Salary range 115k–135k USD with comprehensive benefits.

Qualifications

• Minimum BS in an engineering discipline.
• At least 5 years of experience in medical device project/program management.
• Strong understanding of ISO 13485 and FDA 21 CFR 820 Design Controls.
• Ability to condense and communicate complex ideas to stakeholders.
• Willingness to travel.

Responsibilities

• Lead and coordinate assigned medical device projects, including development activities and manufacturing transfer efforts for components, sub‑assemblies, and finished devices.
• Lead end‑to‑end program lifecycle including planning, execution, monitoring, and closure.
• Transfers to another location, within the network.
• Intercompany collaboration on programs.
• Develop, maintain, and update project schedules, work breakdown structures, task plans, headcount planning and risk documentation to support effective execution and prioritization of project activities.
• Facilitate collaboration across engineering, quality, operations, and other functional teams to drive timely achievement of project deliverables and milestones.
• Monitor project performance with respect to schedule, cost, technical challenges, and risk exposure, with resource planning, and prepare clear status updates for internal leadership and external stakeholders.
• Identify potential project‑level risks and issues early, and implement appropriate mitigation strategies, corrective actions, or preventive measures as needed.
• Ensure required Design History File documentation is created and maintained in compliance with internal procedures and applicable FDA (21 CFR 820) and ISO 13485 requirements.
• Ensure that cost is understood going into operations ramps.
• Lead problem‑solving initiatives and corrective actions.
• Maintain risk registers and contingency plans.
• Apply Lean, Six Sigma, and continuous improvement methodologies.
• Support project teams in defining, documenting, and maintaining product requirements, verification activities, and test plans throughout the development lifecycle.
• Serve as the primary point of contact for customers on assigned projects, coordinating routine communications, meetings, and site visits as appropriate.
• Coordinate with functional and site leadership to align internal resources and capacity in support of project objectives and delivery timelines.

Skills

Project management

MS Project

MS Office

Education

BS in engineering

Tools

MS Office

Job description

Description

About us: For over three decades, Cirtec Medical has been a leading outsourcing partner for complex medical devices. We specialize in providing comprehensive solutions for Class II and III devices, from design and development to precision components and finished device assembly. Our expertise spans neuromodulation, implantable drug delivery, cardiac rhythm management, structural heart, mechanical circulatory support, and minimally invasive surgical systems.

Our dedicated teams prioritize growth, innovation, and collaboration. We actively seek opportunities for improvement to enhance our support for clients. If you embrace a growth mindset and thrive on challenges, you may be a perfect fit for our team!

Position Summary

The Sr. Project Manager position is primarily responsible for managing and coordinating development projects and manufacturing transfer of complex components, sub‑assemblies and/or medical devices.

Key Responsibilities

• Lead and coordinate assigned medical device projects, including development activities and manufacturing transfer efforts for components, sub‑assemblies, and finished devices.
• Lead end‑to‑end program lifecycle including planning, execution, monitoring, and closure.
• Transfers to another location, within the network.
• Intercompany collaboration on programs.
• Develop, maintain, and update project schedules, work breakdown structures, task plans, headcount planning and risk documentation to support effective execution and prioritization of project activities.
• Facilitate collaboration across engineering, quality, operations, and other functional teams to drive timely achievement of project deliverables and milestones.
• Monitor project performance with respect to schedule, cost, technical challenges, and risk exposure, with resource planning, and prepare clear status updates for internal leadership and external stakeholders.
• Identify potential project‑level risks and issues early, and implement appropriate mitigation strategies, corrective actions, or preventive measures as needed.
• Ensure required Design History File documentation is created and maintained in compliance with internal procedures and applicable FDA (21 CFR 820) and ISO 13485 requirements.
• Ensure that cost is understood going into operations ramps.
• Lead problem‑solving initiatives and corrective actions.
• Maintain risk registers and contingency plans.
• Apply Lean, Six Sigma, and continuous improvement methodologies.
• Support project teams in defining, documenting, and maintaining product requirements, verification activities, and test plans throughout the development lifecycle.
• Serve as the primary point of contact for customers on assigned projects, coordinating routine communications, meetings, and site visits as appropriate.
• Coordinate with functional and site leadership to align internal resources and capacity in support of project objectives and delivery timelines.

Must Have

• Minimum BS in a relevant engineering discipline.
• At least 5 years of experience within the medical device industry.
• Minimum 5 years of experience in project / program management of medical device development.
• Must possess strong understanding and working knowledge of ISO 13485 and FDA 21CFR820 based Quality Systems and Design Control.
• Ability to condense and communicate complex technical ideas, project status and risks to internal and external stakeholders.
• Provide clear, data‑driven program updates (KPIs, risks, milestones) to executive leadership.
• Facilitate decision‑making and escalation of critical issues.
• Must have proficiency in MS Project and other MS Office software.
• Must be able to read, write and speak fluent English, and must possess excellent communication skills, both written and oral.
• Willingness to travel, if required.

Good to have

• Experience with metals processing, Catheters, and Nitinol‑based devices preferred but not required.

Salary Range: 115,000 to 135,000 based on skills and experience.

Cirtec Medical Corporation considers for employment and hires qualified candidates without regard to age, race, religion, color, sex, sexual orientation, gender identity, national origin, ancestry, protected veteran or disability status or any factor prohibited by law. Cirtec Medical Corporation and all of its related companies fully endorse equal opportunity for all. Cirtec Medical provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in the job application process.

We work to create a culture that is built on innovation, respect, transparency and communication, and hope you take pride in being a member of our team. It is Cirtec's goal to create a great work environment and to keep the company a great place to work. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. Our benefits include training and career development, healthcare and well‑being programs including medical, dental, vision, wellness and occupational health programs, paid time off and 401(k) retirement savings with a company match.