Sr. Program Manager Engineering

Swoon; Milwaukee (WI); On-site; USD 90,000 - 120,000; Full time

Job summary

A leading healthcare solutions company is seeking a Sr. Program Manager Engineering in Milwaukee, WI. The role focuses on leading remediation projects for medical devices, ensuring compliance with regulations. Ideal candidates will have 5-7 years of project management experience in a regulated industry, strong leadership skills, and a Bachelor’s degree in Engineering. Proficiency in Microsoft tools is required. This position offers the opportunity to impact product quality and regulatory compliance on a global scale.

Qualifications

• 5–7 years of Project Management experience in a regulated industry.
• Strong experience leading cross-functional, global teams.
• Applied knowledge of EU MDR and international medical device regulations.

Responsibilities

• Lead cross-functional teams to remediate on-market medical device products.
• Develop and execute detailed project plans including scope, schedule, budget.
• Coordinate with Engineering, Quality, Regulatory, Manufacturing, and Supply Chain teams.

Skills

Project Management experience

Leading cross-functional teams

Communication skills

Stakeholder management

Leadership skills

Education

Bachelor’s degree in Engineering or technical discipline

Tools

Microsoft Project

Excel

Word

PowerPoint

Job description

We Are Hiring | Sr. Program Manager Engineering – Medical Devices

Contract Duration- 12 Months/W2

About the Role

We are hiring a Project Manager to lead cross-functional remediation projects for a global Medical Devices & Healthcare Products organization. This role focuses on sustaining on-market products and ensuring compliance with EU MDR and international regulatory standards.

You will manage small to medium-scale projects with direct impact on product quality, regulatory compliance, and business continuity while working with globally distributed, multidisciplinary teams.

Key Responsibilities

• Lead cross-functional teams to remediate on-market medical device products to State-of-the-Art and regulatory standards
• Develop and execute detailed project plans including scope, schedule, budget, resources, and risk management
• Coordinate with Engineering, Quality, Regulatory, Manufacturing, and Supply Chain teams globally
• Manage project deliverables, timelines, and cost targets to meet business and quality objectives
• Monitor project progress, manage change control, and address variances using formal change management practices
• Maintain project documentation including RACI charts, metrics, and status reports
• Manage vendor and partner relationships and track labor, expense, and capital expenditures
• Provide regular status updates to senior leadership and key stakeholders

Required Qualifications

• 5–7 years of Project Management experience in a regulated industry
• Strong experience leading cross-functional, global teams
• Applied knowledge of EU MDR and international medical device regulations
• Proven expertise in project scheduling, budgeting, risk management, and vendor management
• Strong communication, stakeholder management, and leadership skills
• Proficiency in Microsoft Project, Excel, Word, and PowerPoint
• Bachelor’s degree in Engineering or a technical discipline

Preferred Qualifications

• Experience as a New Product Development (NPD) or Sustaining Project Manager
• PMP certification or equivalent
• Background in Medical Devices, Life Sciences, or Healthcare products