Date Posted: 09/16/2026
Hiring Organization: Rose International
Position Number: 507585
Industry: Medical Equipment & Supplies
Job Title: Medical Device Project Manager
Job Location: Arlington, TN, USA, 38002
Work Model: Onsite
Shift: 8am to 5pm M-F
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 10
Min Hourly Rate($): 55.00
Max Hourly Rate($): 55.00
Must Have Skills/Attributes: Manufacturing, Project Management, Technical
Experience Desired: Project management experience in a regulated industry (4 yrs); Experience leading cross-functional project teams (4 yrs); Experience managing complex manufacturing or regulatory projects (4 yrs); Medical device industry experience strongly preferred (1 yrs)
Required Minimum Education: Bachelor’s Degree
**C2C is not available**
Job Description
Education Required:
• Bachelor's degree in Engineering, Life Sciences, Regulatory Affairs, Quality, Business, or a related field
Job Requirements:
• Minimum of 4 years of project management experience in a regulated industry.
• Proven experience leading cross-functional teams and driving projects from initiation through completion.
• Experience managing project plans, schedules, budgets, resources, and deliverables.
• Strong knowledge of project management methodologies and best practices.
• Experience identifying project risks and implementing mitigation strategies.
• Ability to manage multiple priorities while meeting project deadlines.
• Experience coordinating with Manufacturing, Quality, Regulatory Affairs, Engineering, and Operations teams.
• Strong understanding of manufacturing processes within a regulated environment.
• Experience supporting or leading regulatory compliance initiatives, preferably EU MDR.
• Excellent organizational, analytical, and problem-solving skills.
• Strong verbal and written communication skills with the ability to present updates to senior leadership and stakeholders.
• Ability to work independently with minimal supervision and exercise sound professional judgment.
• High attention to detail and ability to make informed decisions based on data and factual analysis.
• Proficiency with project management tools such as Microsoft Project, Smartsheet, Jira, or similar software.
• Medical device industry experience preferred.
• Demonstrated ability to influence cross-functional teams without direct authority.
• Commitment to delivering projects on time, within scope, and within budget.
Job Summary:
• Lead cross-functional teams to implement EU MDR manufacturing requirements for the Arlington manufacturing site.
• Develop and execute comprehensive project management plans to ensure successful project delivery.
• Manage project schedules, budgets, resources, timelines, and key deliverables.
• Coordinate efforts across Manufacturing, Quality, Regulatory Affairs, Engineering, and Operations.
• Identify project risks and develop effective mitigation strategies.
• Monitor project progress from initiation through completion, ensuring milestones are achieved.
• Organize project activities and facilitate cross-functional meetings to keep teams aligned.
• Provide regular project status updates and communicate progress to stakeholders and senior leadership.
• Ensure projects remain on schedule, within budget, and compliant with regulatory requirements.
• Resolve project issues using sound judgment and professional expertise.
• Drive collaboration among cross-functional teams to achieve project objectives.
• Work independently with minimal supervision in an individual contributor role.
• Apply technical knowledge and project management expertise to support successful EU MDR implementation.
• Maintain accurate project documentation and ensure effective communication throughout the project lifecycle.
- **Only those lawfully authorized to work in the designated country associated with the position will be considered.**
- **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.**
Benefits:
For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.
California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.
Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.
If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.
Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).
I believe the best thing that Rose HR has going for it is the incredible responsiveness. Everyone is very quick to reply to any concerns, and contacts the contracted employees very quickly and efficiently.
Kevin, Consultant
It is a great pleasure being a part of the Rose International Team.
Toni, Consultant
It was great working for Rose International. Everyone was extremely helpful.
Rosann, Consultant
Your team at Rose International is always very helpful and responsive.
Barbara, Consultant
I am very happy with the Rose International, and the professionalism of the employees.
Robin, Consultant
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