Job Description

Prismatik Dentalcraft is a division of Glidewell Dental.

Essential Functions :

• Prepare and submit product registrations and submissions (510(k), PMA) to FDA and other regulatory bodies.
• Maintains company registrations and device listings in the US, Canada, and the EU.
• Analyzes and reports department metrics.
• Supports and maintains technical files, MDD certifications, and declarations of conformity in support of EU product registrations/CE mark.
• Informs coordinator of product recalls.
• Performs and supports internal, external, and third-party audits.
• Maintains knowledge on current regulations and guidelines.
• Evaluates compliance with applicable regulations, project policies, and procedures
• Reviews and writes standard operating procedures (SOPs) and other RA/QA policies as necessary.
• Collaborates with technical staff to foster understanding of SOPs and guidance documentation.
• Composes audit plans and reports.
• Conducts audits and inspections of GMP and non-regulated documentation.
• Tracks internal and external corrective and preventive actions.
• Performs other related duties and projects as business needs require at direction of management.

Education and Experience:

• Bachelor’s degree in related field preferred
• Minimum five (5) years of experience in Regulatory Affairs.
• Minimum two (2) years of experience in software-based medical devices (e.g., SaMD or SiMD).
• Experience in preparing (writing) domestic and international product submissions, required.

Pay Range: $83,898.06 - 120,000/yr

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