Scrum Master

Software Project Lead (Scrum Master) – Medical Device Software

Work Arrangement: Primarily Remote | Must Be Within Driving Distance of Milwaukee to be in the office 1-2 days per month.

We are seeking a Software Project Lead to support a medical device software development team. This position functions primarily as a Scrum Master, helping an Agile software team stay organized, productive, and focused while also coordinating software documentation required for regulatory submissions.

While this role is largely remote and much of the day-to-day work can be performed from home, candidates must live within driving distance of the Milwaukee/Waukesha area and be available to attend occasional onsite meetings. Corporate preference is approximately 2-3 days onsite per week when needed.

What You'll Do

• Lead Agile software development projects and Scrum activities

• Facilitate sprint planning, daily standups, retrospectives, backlog grooming, and other Agile ceremonies

• Coordinate schedules, timelines, deliverables, risks, and cross-functional communication

• Help maintain project scope and prevent scope creep

• Remove roadblocks and drive accountability across development teams

• Partner with Software Engineering, Quality, and Regulatory teams

• Coordinate software documentation required for regulatory filings and product submissions

• Support a software organization consisting of developers and testers working on desktop software applications used within medical device products

Required Qualifications

• Experience as a Scrum Master, Software Project Lead, Software Project Manager, Technical Project Manager, or similar role

• Strong Agile and Scrum experience leading software development teams

• Experience facilitating meetings and driving projects to completion

• Ability to manage competing priorities, schedules, risks, and scope

• Experience working directly with software developers

• Sufficient technical understanding to participate in software development discussions

• Excellent communication and organizational skills

Preferred Qualifications

• Medical device industry experience

• Experience supporting FDA-regulated software development

• Experience with FDA 510(k), IVDR, IEC 62304, or similar regulatory processes

• Experience coordinating design control, validation, verification, or regulatory documentation

• Experience working with desktop software applications

• Exposure to both Agile and Waterfall development methodologies

This role is an excellent fit for someone who has worked as a Scrum Master or Software Project Lead in a regulated software environment and enjoys keeping teams organized, facilitating productive meetings, managing scope, and ensuring projects move forward successfully. Candidates with medical device software experience and familiarity with regulatory documentation processes will be especially attractive.

Location Requirement: Candidates must reside within driving distance of the Milwaukee area. Although the position is primarily remote, occasional onsite collaboration is expected.

Job Type & Location

This is a Contract to Hire position based out of Schaumburg, IL.

Pay and Benefits

The pay range for this position is $55.00 - $65.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a hybrid position in Schaumburg,IL.

Application Deadline

This position is anticipated to close on Jul 30, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email View email address on click.appcast.io for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.