Date Posted: 08/31/2026
Hiring Organization: Rose International
Position Number: 506621
Industry: Medical Equipment & Supplies
Job Title: Engineering Project Manager - Medical Device & FDA-Regulated Products
Job Location: Salt Lake City, UT, USA, 84111
Work Model: Onsite
Shift: TBD
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 26
Min Hourly Rate($): 69.00
Max Hourly Rate($): 72.50
Must Have Skills/Attributes: Analysis, Mechanical Engineer, PMP
Experience Desired: Medical device or similarly regulated industry (4+ yrs); Strong project management experience leading engineering projects in a technical environment (4+ yrs); Experience working within FDA-regulated environments and familiarity with quality systems, design co (1+ yrs); Proficiency with project management methodologies, tools, and documentation practices (4+ yrs); Knowledge of engineering change management, validation processes, and product lifecycle management (1+ yrs)
Required Minimum Education: Bachelor’s Degree
Preferred Certifications/Licenses: PMP Certification
**C2C is not available**
Job Description
Required Education:
• Bachelor of Science degree in Mechanical Engineering, Biomedical Engineering, Materials Science, or a related technical discipline
Preferred Certifications/Licenses:
• Project Management Professional (PMP) certification
Required Skills/Qualifications:
• Strong project management experience leading engineering projects in a technical environment
• Demonstrated ability to manage multiple projects simultaneously while balancing competing priorities and deadlines
• Excellent organizational, analytical, problem-solving, and decision-making skills
• Ability to work independently with minimal supervision while effectively collaborating with cross-functional teams
• Strong communication and stakeholder management skills, including the ability to present project updates and influence decision-making
• Experience evaluating project risks, implementing mitigation plans, and driving projects to successful completion
• Proficiency with project management methodologies, tools, and documentation practices
Preferred Skills/Qualifications:
• 4+ years of experience within the medical device industry or another highly regulated industry such as pharmaceuticals, biotechnology, aerospace, or manufacturing
• Experience working within FDA-regulated environments and familiarity with quality systems, design controls, risk management, and product development processes
• Knowledge of engineering change management, validation processes, and product lifecycle management
Primary Responsibilities:
• Lead multiple concurrent engineering projects from initiation through completion, ensuring alignment with business objectives, quality standards, and regulatory requirements
• Develop comprehensive project plans, including scope, schedules, resource allocations, budgets, risk assessments, and communication strategies
• Monitor project performance against established milestones, deliverables, timelines, and budgets, proactively identifying risks and implementing mitigation strategies
• Coordinate and prioritize project activities across engineering teams and cross-functional departments to optimize resource utilization and meet project deadlines
• Evaluate, review, and approve project changes that may significantly impact project scope, timelines, budgets, or technical requirements
• Facilitate project meetings, provide status updates to stakeholders and leadership, and maintain clear documentation of project progress and decisions
• Identify operational challenges, technical obstacles, and process inefficiencies, driving resolution efforts to minimize delays and ensure successful project execution
• Collaborate closely with engineering, manufacturing, quality, regulatory affairs, supply chain, and operations teams to ensure project deliverables meet organizational and customer expectations
• Manage relationships with external vendors, consultants, contractors, and suppliers, ensuring performance standards, deliverables, and contractual obligations are met
• Support engineering process improvements and continuous improvement initiatives to enhance project execution, efficiency, and product quality
• Ensure all project activities comply with applicable regulatory standards, industry requirements, and company quality management systems - **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 had a very positive experience working for Rose. The entire process is very efficient and easy.
Joanne, Consultant
Any time I did have a question and called, the phone was always answered, and my question/concern was immediately resolved.
Sally, Consultant
Each time I contacted Rose, I was completely satisfied with the great attention and customer service I received. Each person was extremely knowledgeable and patient with my concerns or questions.
Diana, Consultant
Thanks for the opportunity. If in the future I ever need a job, I would like to work for Rose International.
David, Consultant
The interactions that I have had with your representatives have always been prompt and very professional. I am very pleased and impressed with your company and services.
Sioe, Consultant
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