Intern, Post Market Surveillance Quality
INNOVATION STARTS WITH YOU
Are you interested in working for an organization that is making a difference in people’s lives every day? We’re a medical devices company that develops innovative neuroendovascular technologies for the treatment of vascular disease. We’re a high-growth, customer-focused company with an entrepreneurial spirit producing some of the most reliable and technologically advanced products supported by proven clinical data. Take a closer look at what MicroVention® TERUMO has to offer.
Our summer internship program immerses each intern in an interactive, project-based work environment. Over the span of three months, interns will participate in an in-depth orientation week, facility tours, Leadership Speaker Series Q&A panel, community service activities, baseball games, and beach bashes—all crafted to invest in our interns’ personal and professional development. Year over year, MicroVention continues to have best-in-class conversion rates, converting interns in the following departments: HR, HR Communications, Talent Development, Marketing, R&D, Manufacturing, Quality, Regulatory, Accounting, and more.
Post Market Surveillance-Quality Intern
The Post Market Surveillance Quality Intern will be part of the Post Market Surveillance – Quality organization and will be responsible for facilitating and coordinating the post market surveillance reporting process for all MicroVention product lines. Typical duties might include:
- Plan for the creation of all post market surveillance reports (PMSR)
- Coordinate the collection of all cross-functional information and data for the creation of the reports
- Create, facilitate approval and release of all reports within the documentation system
- Facilitate communication and interactions with the cross functions
- Interact with the global EU MDR Team to prepare the plan for future PMSRs per MDD or European Medical Device Regulations (EU MDR)
- May participate in the creation of Post Market Surveillance Plans per EU MDR
- Performs other duties and responsibilities as needed.
Qualifications
- Working toward Bachelor degree in Regulatory Affairs or Regulatory Affairs certification program.
- Demonstrates a working understanding of regulations.
- Excellent written, verbal and interpersonal communication and computer skills.
- Proven analytical abilities and ability to comprehend technical documents and concepts.
- Ability to work independently, manage multiple priorities effectively and foster collaboration.
Additional Information
- The primary work location for this position is Aliso Viejo, CA (company headquarters).
- Relocation may be available for qualified candidates.
- Candidates must be eligible to work in the U.S. and not require visa sponsorship.
- For more information, visit our website at www.microvention.com and our LinkedIn page at https://www.linkedin.com/company/microvention/life/ur.