Job Description

Role:

Coordination and project support (including international submissions, product release) Responsibilities

• Supporting international submissions
• Product release
• Tracking deliverables, coordinate team activities, and perform status updates
• Participates in projects supporting RA product teams and performs other related duties and responsibilities, as assigned

Years Experience:

• 1+ years experience in a medical device or similarly regulated industry

Skills:

• Ability to schedule and organize multiple projects

Education:

• BS Engineering or Scientific

Duties:

• Manager regulatory submissions ot ensure timely regulatory approval of medical devices.
• Monitor changing regulations in geographies and translate/communicate these requirements to project development and/or continuous improvement project teams.
• Ensure all client product and procedures comply with applicable regulatory agency requirements and guidelines.

Job Type: Contract

Salary: $17.39 - $27.00 per hour

Schedule:

• 8 hour shift
• Day shift

Ability to commute/relocate:

• Saint Paul, MN 55117: Reliably commute or planning to relocate before starting work (Required)

Education:

• Bachelor's (Preferred)

Experience:

• regulatory affairs: 2 years (Preferred)
• international submissions: 1 year (Preferred)

Work Location: One location

Similar Jobs