Senior Project Engineer

Roper Technologies • $95K — $115K *
Healthcare
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • 5-7 years of experience leading complex cross-functional projects with minimal oversight.
  • In-depth knowledge of medical device design controls, quality assurance, and regulatory requirements.
  • Bachelor's degree in engineering or a related field preferred; equivalent experience may be accepted.
  • Experience at Project Engineer II level or equivalent role for at least 3-5 years.

Responsibilities

  • Develop and manage comprehensive project plans with clear scope and objectives.
  • Lead project team meetings, ensuring documentation of actions and follow-ups.
  • Identify project risks, propose mitigation strategies, and communicate with leadership.
  • Collaborate with teams using structured problem-solving approaches for project challenges.
  • Create and manage resource and budget forecasts considering various trade-offs.
  • Ensure compliance with design control standards and regulatory policies.
  • Deliver timely project status updates to internal and external stakeholders.

Benefits

  • Performance bonuses and competitive compensation.
  • Comprehensive benefits package starting on day one.
  • Company-sponsored health plans and 401(k) matching.
  • Tuition reimbursement and paid leave options.
  • Opportunities for flexible scheduling and part-time telecommuting.
Full Job Description
Summary:

The Senior Project Engineer leads CIVCO's large, complex, and most visible projects or programs with limited oversight. This role integrates business, technical, regulatory, quality, customer, supplier, financial, and organizational considerations; brings clear recommendations to leadership; mentors other Project Engineers; and improves project execution practices.

Senior Project Engineer is based out of our production facility in Coralville, IA. This position may have opportunities for flexible scheduling and part-time telecommuting based on business needs.

Job Requirements:

  • Project Planning: Develop and maintain project plans, including scope, objectives, and timelines. Ability to propose tailored project approaches (waterfall, agile, hybrid) based on understanding of scope and delivery target.
  • Meeting Coordination: Organize, lead, and actively participate in project team meetings, ensuring action items are accurately documented, assigned, and completed on schedule.
  • Risk Identification and Recovery: Monitor project progress against established plans, identify potential risks, and escalate concerns with prepared risk mitigation options promptly to leadership.
  • Collaboration & Problem Solving: Partner with internal teams to apply structured problem-solving methodologies to assigned tasks and project challenges.
  • Resource & Financial Management: Develop credible resource and budget forecasts that frame opportunity-cost, cost-benefit, make-or-buy, dual-source, and sequencing tradeoffs for leadership.
  • Regulatory Compliance: Ensure all design control activities comply with applicable standards, regulations, and company policies.
  • Quality & Change Management: Apply CIVCO's quality and change management processes consistently and effectively across all responsibilities.
  • Reporting & Communication: Prepare and deliver clear, timely project status updates for internal and external stakeholders.
  • Stakeholder Leadership: Manage executive, customer, OEM, and senior cross-functional communication; create clarity around decisions, risks, implications, and required actions; and lead through conflict, uncertainty, resistance, and competing priorities.
  • Mentorship & Process Improvement: Mentor Project Engineer I and II employees, provide practical feedback, review plans and decision framing, model disciplined governance compliance, and lead department-level process improvements and training


To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.

Qualifications:

  • Demonstrated success leading large or complex cross-functional projects with limited oversight.
  • Strong working knowledge of medical-device design controls, quality systems, regulatory considerations, verification and validation, risk management, project financials, and executive communication.


Education and/or Experience:

  • Bachelor's degree in engineering or a related technical discipline preferred; equivalent relevant experience may be considered.
  • Typically 6-12 years of relevant experience, often including 3-5 years at the Project Engineer II level or equivalent demonstrated capability.


What Makes You Stand Out:

  • Familiarity with stage-gate or similar structured development frameworks.
  • Basic understanding of design verification/validation and regulatory considerations in product development (ISO 13485, 14971, 10993, etc.).
  • Experience with FDA and EU regulatory environments, human factors, supplier development, customer programs, or complex product-development portfolios.
  • Demonstrated mentorship and implementation of process improvements that strengthened project execution, forecasting, risk management, or cross-functional collaboration.
  • Experience using project governance and reporting tools such as Microsoft Project, SharePoint, and Power BI.


What You Will Get:

At CIVCO, we empower our associates to develop their careers while furthering our mission to make image-guided medical procedures safer. We offer competitive compensation, performance bonuses, and a complete benefits package starting day one - including company-sponsored health plans, 401(k) matching, tuition reimbursement, paid leave, and more.

Physical Demands:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

While performing the duties of this job, the employee is regularly required to sit; reach with hands and arms and talk or hear. The employee is frequently required to use hands to finger, handle, or feel. The employee is occasionally required to stand; walk; climb or balance and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, color vision, depth perception and ability to adjust focus.

Work Environment:

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

While performing the duties of this job, the employee is frequently exposed to moving mechanical parts. The employee is occasionally exposed to toxic or caustic chemicals and risk of electrical shock. The noise level in the work environment is usually moderate.

About Roper Technologies

Roper Technologies is a diversified technology company that designs, develops, and manufactures engineered products and solutions for global niche markets. The company operates through four segments: Application Software; Network Software & Systems; Measurement & Analytical Solutions; and Process Technologies. Roper Technologies serves customers in healthcare, transportation, food, energy, water, education, and other markets. The company was founded in 1981 and is headquartered in Sarasota, Florida.
Learn more about Roper Technologies
Size
19,300 employees
Market Cap
$45.7 billion
Industry
Net Income
$949.6 million
5 Year Trend
+8.8%
Revenue
$5.5 billion
NASDAQ

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