Project Manager

Description

100% Onsite

The candidates must have project management experience and some type of medical device/industry experience.

They must have an understanding of a regulatory role.

Responsibilities:

• Collaborate on IVDR changes with various departments.
• Manage interactions between internal teams and TPMs.
• Coordinate international projects and teams.
• Support business process improvements.
• Run effective meetings and set clear goals with deadlines.
• Identify and resolve issues, mitigating project delays.
• Manage multiple projects, ensuring timely completion.
• Ensure design and regulatory compliance. Use PFMEA to drive product quality improvements.

Additional Details:

• Must be a self-starter.
• Microsoft skills required.
• Ability to keep deadlines/timeframes.
• Able to work cross functionally.
• Flexibility with evening calls (not daily).
• One year of experience minimum needed with the ability to function with product transfer with regulatory, quality and other departments.

Education:

• Associate's and/or Bachelor's degree in fields like project management/business administration/a related area or an equivalent combination of education and experience.
• 3+ years of experience in project management required.