More jobs:
Regulatory Affairs Associate
Job in
Scottsdale, Maricopa County, Arizona, 85261, USA
Listed on 2026-02-15
Listing for:
Innovative Health LLC
Full Time
position Listed on 2026-02-15
Job specializations:
-
Healthcare
Healthcare Compliance
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.
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.)
Position Requirements
10+ Years
work experience
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
Search for further Jobs Here:
×