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Medical Device Project Manager Jobs in Texas (NOW HIRING)

We are seeking a Project Manager to support the planning and execution of medical device and aesthetics product development projects within our Commercialization / Project Management team. Reporting ...

Accredited Project Management certification, such as PMP or Scrum Master. * Strong Technical Experience with MDM (Mobile Device Management) implementation/migration on an enterprise scale. * 7+ years ...

Accredited Project Management certification, such as PMP or Scrum Master. * Strong Technical Experience with MDM (Mobile Device Management) implementation/migration on an enterprise scale. * 7+ years ...

Medical Device Rep

Austin, TX · On-site

$82K - $113K/yr

Medical Sales Territory Representative - Entry Level We are a leading Medical Device and Equipment ... Ability to effectively manage a physician-based customer base * Skills to communicate clinically ...

We are seeking an experienced Project Manager to lead the implementation of European Union Medical Device Regulation (EU MDR) requirements at our Arlington manufacturing site. This role will be ...

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Medical Device Project Manager information

What are the day-to-day responsibilities of a Medical Device Project Manager?

As a Medical Device Project Manager, your daily duties typically include coordinating the activities of cross-functional teams—such as engineering, quality assurance, regulatory affairs, and marketing—to ensure project milestones are met. You'll oversee timelines, budgets, and documentation, while also addressing risks, facilitating communication, and managing stakeholder expectations. Regular tasks might involve leading project meetings, updating project trackers, monitoring regulatory compliance, and troubleshooting challenges that arise throughout the product development lifecycle. Successful project managers balance strategic planning with hands-on problem solving to keep complex medical device projects moving smoothly toward launch.

What is a Medical Device Project Manager job?

A Medical Device Project Manager oversees the planning, development, and launch of medical devices, ensuring compliance with regulatory standards. They coordinate cross-functional teams, manage timelines, budgets, and risks, and facilitate communication between stakeholders. Their role involves working closely with engineering, regulatory, quality, and marketing teams to bring safe and effective medical devices to market.

What are the key skills and qualifications needed to thrive in the Medical Device Project Manager position, and why are they important?

To thrive as a Medical Device Project Manager, you need a strong knowledge of medical device development, regulatory compliance, and project management, often supported by a background in engineering or life sciences and certifications like PMP or Six Sigma. Familiarity with tools such as Microsoft Project, quality management systems (QMS), and regulatory submission platforms (such as FDA eSubmitter) is highly valuable. Excellent leadership, problem-solving skills, and effective communication are essential for coordinating cross-functional teams and navigating complex project demands. These skills are crucial for delivering compliant, high-quality medical devices on time and within budget while ensuring collaboration across technical and clinical stakeholders.

What cities in Texas are hiring for Medical Device Project Manager jobs? Cities in Texas with the most Medical Device Project Manager job openings:
Infographic showing various Medical Device Project Manager job openings in Texas as of July 2026, with employment types broken down into 79% Full Time, 7% Part Time, and 14% Contract. Highlights an 95% In-person, and 5% Remote job distribution.
Project Manager, Medical Device

Project Manager, Medical Device

Revance

Dallas, TX • Remote

$8.0K - $105K/yr

Full-time

Medical, Retirement, PTO

Posted 19 days ago


Job description

Job Summary:

We are seeking a Project Manager to support the planning and execution of medical device and aesthetics product development projects within our Commercialization / Project Management team. Reporting into a Program Manager, this role will own day-to-day project management activities, including timeline development, milestone tracking, risk identification, and cross-functional coordination.

The ideal candidate will bring strong project management skills, knowledge of device and aesthetics product development, and familiarity with related regulatory pathways. PMP certification and prior medical device experience are preferred.

  • Reporting to: Technical Program Manager
  • Location: Remote 
  • Salary Range: $80,00-$105,000 annually + annual performance bonus 

the final salary offered will depend upon factors that may include but are not limited to the quality and length of experience, education and geographic location.

Responsibilities/Essential Duties:

  • Manage the execution of assigned projects from initiation through launch, ensuring alignment with overall program goals.
  • Develop and maintain detailed project plans, outlining deliverables, dependencies, risks, and milestones.
  • Proactively manage, monitor and control scope creep, risks, project budgets and schedule health.
  • Lead cross-functional project meetings to align priorities, track progress, and drive accountability across teams.
  • Facilitate collaboration across R&D, Regulatory, Quality, Supply Chain, Operations, Marketing, and Packaging teams.
  • Track and report project status, escalating risks or roadblocks to the Program Manager and leadership as needed.
  • Support regulatory and quality strategies, ensuring compliance with FDA and international submission requirements (e.g., 510(k)).
  • Partner with external suppliers, such as CMOs, to ensure integrated execution.
  • Maintain project documentation and dashboards within PM tools (e.g., Smartsheet, Monday.com, MS Project).
  • Assist in continuous improvement initiatives to strengthen project management practices across the organization.

Basic Qualifications:

  • Bachelor’s degree in engineering, life sciences, or related field; advanced degree a plus.
  • 3–5+ years of project management experience in regulated industries (medical devices or aesthetics/skincare).

Preferred Qualifications:

  • Experience with regulatory pathways, including 510(k).
  • Demonstrated success managing projects through regulatory, clinical, and/or commercial milestones.
  • PMP certification (or equivalent) preferred.
  • Proficiency with project management tools such as Smartsheet, Monday.com, or MS Project.
  • Strong communication skills, with ability to translate technical details into clear, actionable updates.
  • Highly organized, proactive, and comfortable working in a fast-paced, cross-functional environment.

Company Summary:

Revance is a fast-growing global aesthetics and skincare company focused on providing innovative aesthetics and market-leading skincare offerings throughout every stage of life. With a differentiated portfolio of products spanning 60 countries, Revance meets the evolving needs of patients and consumers worldwide through continued innovation and commercialization of new products and treatments.

What Revance invests in you:

  • Competitive Compensation including base salary and annual performance bonus,
  • Flexible unlimited PTO,  holidays, weeks parental leave
  • Generous healthcare benefits, Employer HSA match, 401k match, tuition reimbursement, wellness discounts and much more

 

This section of the job description is required by the American with Disability Act (ADA). The ADA requires that job descriptions reflect the physical and mental demands required to effectively perform the essential duties of the job. The ADA prohibits employers from discriminating against a “qualified individual with a disability” in all aspects of the employment relationship. A “qualified individual with a disability” is “an individual who meets the education, experience, skill, and other job-related requirements of a position held or desired, and who, with reasonable accommodation, can perform the essential functions of a specified job.” 

Revance is an Equal Opportunity employer. All qualified applicants will receive consideration for employment based on merit, without regard to race, color, religion, sex, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.