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Project Manager - Contract

  • Marlborough, MA, United States

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Job details

Experience
5+ years' experience in medical device industry, required.
Posting language
English
Posted

Original job description

Project Manager - Contract

DISHER is seeking an experienced Project Manager to join our customer team for a 6-month project onsite in Marlborough, MA. Project Manager will be responsible for leading weekly meetings. working with project teams to maintain and develop plans, coordinate and track external development, and work cross functionally. Work may require up to 15% of travel.

What it's like to work here

Make a positive difference! It’s why we exist. We are always looking for teammates who are eager to use their diverse set of talents with our customers, coworkers, and communities. We want to leave this world better than we found it.

What you will get to do:

  • Support research and development team, consultants, and contract companies to ensure medical devices and equipment software are design and developed on time, within budget, and according to company procedures.
  • Lead weekly project tactical meetings to ensure weekly tasks are planned and coordinated.
  • Work with project teams to create and maintain development plans for projects from conception through commercialization. Collaborate with the project team to define project objectives, requirements, and assumptions necessary to structure a project or activity.
  • Coordinate and track external development, testing, and production vendor timelines.
  • Support preclinical studies including planning, preparation, and execution.
  • Work with Quality, Clinical and Regulatory personnel to support regulatory submissions.
  • Ensure all design and development activities adhere to regulatory requirements (e.g., FDA, ISO 13485, IEC 62304, MDR).

What will make you successful:

  • Bachelor’s degree in an Engineering or Scientific related field required (master's degree preferred).
  • 5+ years' experience in medical device industry, required.
  • Understanding of medical device regulations (FDA, ISO 13485, IEC 62304, and MDR), required.
  • Experience creating and managing project plans with critical chain project management tools, required.
  • Strong understanding of critical chain project management principles, including buffer management, preferred.
  • Experience managing 2-3 programs concurrently, preferred.
  • Excellent communication skills, capable of driving cross functional and global teams, preferred.
  • Ability to effectively manage scope changes and perform impact assessments, preferred.
  • Strong organizational skills with attention to detail, especially for regulatory compliance documentation, preferred.
  • Ability to adapt quickly in a fast-paced, evolving company and operate with a high sense of urgency, preferred.
  • Willing to travel up to 15% (may be required).

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More about this job

Skills

  • Research
  • Medical devices
  • Medical device regulations
  • Project management
  • Project management principles
  • Communication skills
  • Organizational skills
  • Attention to detail
  • Regulatory compliance
  • Documentation

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