Extracted from the posting
TL;DR
Contract Project Manager for a 6-month onsite role in Marlborough, MA, supporting medical device R&D and software development. Responsibilities include leading weekly project meetings, maintaining development plans from conception through commercialization, and coordinating external development, testing, and production vendor timelines. Requires 5+ years in medical device industry and knowledge of FDA, ISO 13485, IEC 62304, and MDR regulations.
The full posting
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:
Company stack
This posting doesn’t list technologies. These are the ones DISHER uses across its other roles.