Job Description
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, ISO13485, 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.)
Disclaimer: This job listing is sourced from LinkedIn and is provided for informational purposes. Apply directly through the employer’s application process. Medical Device Navigator is not affiliated with the hiring company.