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



Regulatory Affairs Specialist

Job Description:

This position is responsible for assisting in obtaining regulatory approvals and ensuring compliance to FDA and international regulatory agency requirements including ISO, local, state and/or federal requirements. Job duties:

  • Serves as a member on project teams completing tasks as assigned by the team.

  • Aides in the execution of the regulatory plan for the assigned market(s) based on the approved regulatory strategy.

  • Assists in preparing regulatory submissions to ensure MicroVention devices are commercially available in the assigned market(s) based on the approved regulatory strategy.

  • Aides in integrating various sources of information into a uniform style and language for regulatory submissions.

  • Documents, consolidates and maintains verbal and written communication with regulatory agencies.

  • Maintains regulatory files and records.

  • Assists in reviewing change order documents and ascertains impact on current regulatory approvals.

  • Assists with technical publishing of submissions.

  • Supports and contributes into editing/revising Standard Operating Procedures.

  • Builds team cohesiveness by supporting team members.

  • Performs other duties and responsibilities as assigned.

Auto req ID:



Aliso Viejo, California, USA

Department Name:

523-RAQA Regulatory


  1. Minimum BA/BS degree in a scientific or technical discipline or relevant field of study. Advanced degree may offset medical device industry experience.

  2. Minimum of three (3) years of Medical Device/Pharma industry experience.

  3. Must read/write Mandarin/English.

Desired Qualifications

  1. Minimum one (1) year Regulatory Affairs Experience.

  2. Leadership skills.

  3. Ability to work well in a team environment.

  4. Detail oriented.

  5. Proven analytical abilities and organization skills.

  6. Ability to comprehend technical documents and concepts.

  7. Proficient computer skills (e.g., MS Office).

External-Facing Title:

Regulatory Affairs Specialist

Posting Country:

US - United States

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.