Senior R&D Project Manager - New Product Development Orthopedics
CONMED Corporation, Largo, FL, United States
Overview
The
Senior R&D Project Manager
will be responsible for overseeing and managing the development of new orthopedic products from concept to market launch. The ideal candidate will have a proven track record of successfully managing complex projects within the medical device or any other regulated industry and must have a PMP certification.
Responsibilities
Project Planning and Scheduling: Develop and maintain detailed project plans, including timelines, milestones, and deliverables. Utilize project management software to track progress and ensure adherence to schedules.
Cost and Budget Management: Prepare and manage project budgets, ensuring projects are completed within financial constraints. Monitor expenditures and implement cost-saving measures as necessary.
Risk Management: Identify potential project risks and develop mitigation strategies. Conduct regular risk assessments and adjust plans as needed to address emerging issues.
Quality Management: Ensure compliance with regulatory requirements and industry standards throughout the product development process. Implement quality control measures to maintain high standards.
Stakeholder Management: Collaborate with R&D, Quality, Regulatory, Manufacturing, and Marketing teams to ensure alignment and successful project execution. Communicate project status and updates to senior management and stakeholders.
Resource Management: Allocate resources effectively to meet project objectives. Coordinate with team members and departments to ensure optimal resource utilization.
Performance Monitoring and Reporting: Conduct regular project status meetings and provide comprehensive updates to senior management. Utilize performance metrics to track project progress and identify areas for improvement.
Continuous Improvement: Drive continuous improvement initiatives within the project management process. Implement best practices and lessons learned from previous projects.
Team Leadership and Development: Mentor and guide junior project managers and team members. Foster a collaborative and innovative work environment.
Qualifications
Bachelor’s degree in biomedical engineering is preferred but other engineering degrees will also be considered.
5 to 10 years of experience in project management preferably within the medical device industry, with a focus on new product development, PMP ( Project Management Professional) certification highly preferred.
Preferred Qualifications
Strong knowledge of design controls and regulatory requirements for medical devices.
Proven ability to manage multiple projects simultaneously and deliver results on time and within budget.
Excellent leadership, communication, and interpersonal skills.
Strong problem-solving and decision-making abilities.
Proficiency in project management software and tools (Smartsheet, MS Project, etc).
Expected Travel 0-20%
This position is not eligible for employer-visa sponsorship
This job posting is anticipated to close on April 6, 2026. We may, however, extend this time period, in which case the posting will remain available on careers.conmed.com. Please submit your application as soon as possible as we will be reviewing applications on a rolling basis as we receive them.
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The
Senior R&D Project Manager
will be responsible for overseeing and managing the development of new orthopedic products from concept to market launch. The ideal candidate will have a proven track record of successfully managing complex projects within the medical device or any other regulated industry and must have a PMP certification.
Responsibilities
Project Planning and Scheduling: Develop and maintain detailed project plans, including timelines, milestones, and deliverables. Utilize project management software to track progress and ensure adherence to schedules.
Cost and Budget Management: Prepare and manage project budgets, ensuring projects are completed within financial constraints. Monitor expenditures and implement cost-saving measures as necessary.
Risk Management: Identify potential project risks and develop mitigation strategies. Conduct regular risk assessments and adjust plans as needed to address emerging issues.
Quality Management: Ensure compliance with regulatory requirements and industry standards throughout the product development process. Implement quality control measures to maintain high standards.
Stakeholder Management: Collaborate with R&D, Quality, Regulatory, Manufacturing, and Marketing teams to ensure alignment and successful project execution. Communicate project status and updates to senior management and stakeholders.
Resource Management: Allocate resources effectively to meet project objectives. Coordinate with team members and departments to ensure optimal resource utilization.
Performance Monitoring and Reporting: Conduct regular project status meetings and provide comprehensive updates to senior management. Utilize performance metrics to track project progress and identify areas for improvement.
Continuous Improvement: Drive continuous improvement initiatives within the project management process. Implement best practices and lessons learned from previous projects.
Team Leadership and Development: Mentor and guide junior project managers and team members. Foster a collaborative and innovative work environment.
Qualifications
Bachelor’s degree in biomedical engineering is preferred but other engineering degrees will also be considered.
5 to 10 years of experience in project management preferably within the medical device industry, with a focus on new product development, PMP ( Project Management Professional) certification highly preferred.
Preferred Qualifications
Strong knowledge of design controls and regulatory requirements for medical devices.
Proven ability to manage multiple projects simultaneously and deliver results on time and within budget.
Excellent leadership, communication, and interpersonal skills.
Strong problem-solving and decision-making abilities.
Proficiency in project management software and tools (Smartsheet, MS Project, etc).
Expected Travel 0-20%
This position is not eligible for employer-visa sponsorship
This job posting is anticipated to close on April 6, 2026. We may, however, extend this time period, in which case the posting will remain available on careers.conmed.com. Please submit your application as soon as possible as we will be reviewing applications on a rolling basis as we receive them.
#J-18808-Ljbffr