Project Manager - Bridgewater, United States - Capabilix

Capabilix
Capabilix
Verified Company
Bridgewater, United States

3 weeks ago

Mark Lane

Posted by:

Mark Lane

beBee recruiter
Description

Job Title:
Project Manager (Medical Devices)

Location:
Remote

Duration: 6 Months

Job Summary:


In this role, you will play a pivotal role in leading and managing the development of new medical devices, from concept to commercialization.

You will be responsible for overseeing all aspects of the project lifecycle, ensuring projects are completed on time, within budget, and meet all regulatory requirements.


Responsibilities:


  • Develop and manage comprehensive project plans, including timelines, milestones, budgets, and resource allocation.
  • Lead crossfunctional teams of engineers, designers, regulatory specialists, and marketing professionals.
  • Manage project risks and proactively identify and mitigate potential issues.
  • Facilitate communication and collaboration between internal and external stakeholders.
  • Monitor project progress and provide regular status reports to senior management.
  • Ensure compliance with all relevant regulatory standards (e.g., FDA, ISO).
  • Manage project budgets and track expenditures.
  • Contribute to the development and implementation of project management processes.
  • Identify and implement process improvements to enhance efficiency and effectiveness.
  • Participate in the development of new product concepts and feasibility studies.

Qualifications:


  • Bachelor's degree in Engineering, Project Management, or a related field (Master's degree preferred).
  • Minimum 5 years of experience in project management, preferably within the medical device industry.
  • Proven track record of successfully leading and managing complex projects from conception to completion.
  • Strong understanding of project management methodologies (e.g., Agile, Waterfall).
  • Excellent analytical and problemsolving skills.
  • Strong communication, interpersonal, and leadership skills.
  • Ability to work effectively in a fastpaced and dynamic environment.
  • Proficient in Microsoft Office Suite (Word, Excel, PowerPoint) and project management software.
  • A strong understanding of regulatory requirements for medical devices (FDA QSR, etc.) is a plus.

Skills:


  • Excellent communication skills.
  • Project management expertise.
  • Risk management strategies.
  • Crossfunctional coordination.
  • Customer success.
  • Quality assurance measures.
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