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Regulatory Affairs Associate

Job in Scottsdale, Maricopa County, Arizona, 85261, USA
Listing for: Innovative Health LLC
Full Time position
Listed on 2026-02-15
Job specializations:
  • Healthcare
    Healthcare Compliance
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

The Regulatory Affairs Associate role is responsible for assisting with preparing and submitting the appropriate documentation for pre-market submissions (i.e. FDA 510(k) submissions, Health Canada Device License Applications). This role also supports post-market regulatory compliance activities.

Role and Responsibities:
  • Assisting with responses to deficiency letters and other requests for documentation for submissions.
  • Reviews complaints/adverse events for submission of MDRs;
  • Review and approve test protocols/reports and other documentation/information for regulatory submissions from various functional areas and check for errors, legibility, and missing information;
  • Assist with the development of labeling and ensure compliance with applicable regulations;
  • Participate in project development teams and review plans, reports, risk management, risk assessments and design reviews associated with product and process projects;
  • Provide regulatory assessments for manufacturing, line extensions, design changes, and validation activities;
  • Conduct regulatory review and approval of change orders and related project documentation;
  • Implement and maintain unique identifier (UDI) activities for compliance;
  • Assists with PFMEA risk assessments;
  • Assists in archiving regulatory documentation and maintaining related databases;
  • Participate in internal and external audits;
  • Assist with other Regulatory projects and activities as required.
Education and

Qualifications:
  • Minimum of Bachelor's degree (preferably in (i.e. Engineering, Biological Sciences, or other technical field) or equivalent education, training and experience;
  • Minimum of one (1) year medical device regulatory and/or quality experience;
  • Basic knowledge of FDA 21 CFR Part 820, ISO
    13485, and 510(k) submission requirements preferred;
  • Basic knowledge of Canadian Medical Device Regulations, MDD, MDSAP and ISO standards preferred;
  • High degree of initiative, be able to balance a variety of tasks, and with strong organizational abilities;
  • Strong commitment to quality, accuracy and detail;
  • Excellent oral & written communications skills;
  • Excellent interpersonal skills are required, due to the numerous internal customers with varying and unique requirements/ priorities. Must understand the nature of the work and the impact it has on the organization.
  • Ability to work in a fast paced/entrepreneurial team environment;
  • Proficient in computer applications (i.e. Microsoft Office, Word, PowerPoint, Excel, etc.)
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Position Requirements
10+ Years work experience
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