Project Manager | Recovery Sciences

Enovis Corporation (NYSE: ENOV) is an innovation-driven medical technology growth company dedicated to developing clinically differentiated solutions that generate measurably better patient outcomes and transform workflows. Powered by a culture of continuous improvement, global talent, and innovation, the Company’s extensive range of products, services, and integrated technologies fuels active lifestyles in orthopedics and beyond.

About the role

At Enovis™ we pay attention to the details. We embrace collaboration with our partners and patients, and take pride in the pursuit of scientific excellence — with the goal of transforming medical technology as we know it. As a key member of the Recovery Sciences team, you will play an integral part in helping Enovis drive the medical technology industry forward through transforming patient care and creating better patient outcomes.

Enovis’ Recovery Sciences business is the leading global provider of high-quality clinical equipment for rehabilitation and pain management used by physical therapists, occupational therapists, athletic trainers, and chiropractors. To improve our position even further, Recovery Sciences is focused on accelerating the pace of new product development and better integrating our global product offering to meet the changing needs of clinicians. Recovery Sciences R&D supports Chattanooga, LightForce, Companion, and Compex brands.

The Project Manager will lead cross-functional teams to deliver new products to the market with a goal of reducing time to market while significantly improving launch success. Due to the dynamic nature of the business, this role will also lead strategic initiatives on product development process improvement and growth objectives such as acquisitions.

Location: Lewisville, Texas (Hybrid - 3 days onsite, 2 days remote)
Reports To: Sr Engineering Manager, PMO | Recovery Sciences

Responsibilities

• Engineering Project Management
  • Manage New Product Development Projects from feasibility phase to final product launch, in collaboration with the PMO Manager and the Recovery Sciences leadership team.
  • Develop and maintain a project plan to achieve Business case objectives; identify variations to plan, mitigate them, and execute changes as needed.
  • Identify, manage, and mitigate project risks.
  • Ensure that the project is delivered achieving the specification, timeline, and cost targets.
  • Lead & influence cross-functional project teams, including internal and external stakeholders (Marketing, Regulatory, Quality, Supply Chain, Manufacturing, Engineering).
  • Manage all project team meetings and all operational activities needed by the project.
  • Establish and execute a communication plan to keep all levels of the organization informed as necessary.
  • Develop in collaboration with other departments the entire project documentation (DHF), following Enovis procedures.
  • Understand medical devices development regulatory environment.
• Strategy Development
  • Understand market trends, healthcare professional’s needs, competitive strategies, etc., and use this knowledge to guide development of plans and products.
  • Actively solicit voice of the customer input, including physicians, allied health care providers, sales consultants, and distributors, to understand clinical needs and trends to develop incremental and/or new-to-world products.
  • Support target identification, due diligence, and integration activities for acquisitions and business partnerships.
• Continuous Improvement
  • Work with R&D, Regulatory, Marketing, and Supply Chain leaders to improve the New Product Development process.
  • Develop and improve third-party relationships that can increase the capacity, efficiency, and effectiveness of Recovery Sciences’ NPD efforts.
  • Develop competency in the most relevant CBS tools, including Accelerated Product Development, Root Cause Countermeasure, and Transactional Process Improvement.

Requirements

• Bachelor in Engineering.
• 5-7 years work experience in Project Management in a highly regulated environment.
• Experience with medical device product development is a plus.
• Experience on Software products development is a plus.

Skills

• Motivation and interest to work in the highly regulated medical devices world.
• Ability to influence individuals and groups to resolve conflicts and achieve objectives.
• Risk-based decision driven.
• Process improvement mindset.
• Additional beneficial skills: PMP certification or similar training.

Travel

As needed. Estimated 20% of time.

Benefits

• Medical Insurance
• Dental Insurance
• Vision Insurance
• Spending and Savings Accounts
• 401(k) Plan
• Vacation, Sick Leave, and Holidays
• Income Protection Plans
• Discounted Insurance Rates
• Legal Services