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Welcome to SVA’s jobs portal, your one-stop shop for finding the most up to date source of employment opportunities. We have partnered with the National Labor Exchange to provide you this information. You may be looking for part-time employment to supplement your income while you are in school. You might be looking for an internship to add experience to your resume. And you may be completing your training ready to start a new career. This site has all of those types of jobs.

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MicroVention, Inc. Intern, Regulatory Affairs in Aliso Viejo, California

12152BR

Title:

Intern, Regulatory Affairs

Job Description:

Are you interested in working for an organization that is making a difference in people’s lives every day? We’re a high-growth company, customer-focused 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.

Regulatory Affairs (RA) Intern

The Regulatory Affairs team is responsible for executing regulatory strategies, submissions, interactions with regulatory authorities, and supports business by obtaining regulatory approvals for MicroVention® TERUMO products.

As a Regulatory Affairs Intern, you will learn the product development process through a regulatory perspective and the requirements of the various countries worldwide in order to get products into their markets. You will review elements of risk management, design control documents and scientific testing that support a registration. You will also gain access to design team dynamics, requirements and deliverables through shadowing; thereby allowing you to draw on your scientific or technical background to make regulatory assessments. Valuable analytical and critical thinking skills will be honed during your time with the regulatory group.

Responsibilities:  

  • Familiarize with the design, manufacture, and the clinical use of the MicroVention products

  • Perform specific regulatory tasks in support of a regulatory filing for new/modified product and any planned renewal of regulatory registrations (FDA, EU or Health Canada)

  • Partner and collaborate with R&D, Operations, Quality, Labeling, and Marketing to help establish project deliverables to support regulatory submissions

  • Shadow and/or partner with a senior regulatory professional(s) to learn and interpret regulations and implement them on the assigned project(s)Learn regulatory affairs competencies to ensure product registration lifecycle processes compliance

  • Performs other duties and responsibilities as assigned.

Auto req ID:

12152BR

Location:

Aliso Viejo, California, USA

Department Name:

523-RAQA Regulatory

Qualifications:

Required Qualifications

  • Working toward Master’s degree in Regulatory Affairs or related field.

  • 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 and manage multiple priorities effectively.

Additional Information

 

  • The primary work location for this position is Aliso Viejo, CA (company headquarters)

  • Candidates must be eligible to work in the U.S. and not require visa sponsorship.

  • Relocation may be available for qualified candidates.

External-Facing Title:

Intern, Regulatory Affairs

Salary Range:

$19.00 - $27.00/hour (can be higher based on education, experience or skill set)

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.

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