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Scanlan International

Regulatory Affairs Specialist

Pay: Not specified
Posted: 1 week ago
Location: Saint Paul, MN (Onsite)
Last Updated: 1 week ago
Hours: Full-Time
Expires: 9/29/2026

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What they do

A Regulatory Affairs Specialist maintains specialized knowledge of state and federal government regulations that affect an employer. Interprets regulations and implements procedures that bring an employer into compliance with regulations; may audit internal compliance with regulations.

$97,974 / year median in Minnesota

+1% projected growth

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Job Description

Regulatory Affairs Specialist Scanlan International - 3.9 Saint Paul, MN Job Details Full-time 23 hours ago Qualifications Technical editing Record keeping Bachelor's degree Desktop applications Biomedical regulatory compliance Productivity software Technical Proficiency Customer complaint resolution Full Job Description The Regulatory Affairs Specialist will assist in maintaining market authorizations for Scanlan products, including design files, technical documentation, product registrations and listings. They will also assist with post-market surveillance and post-delivery regulatory activities necessary to ensure Scanlan products remain state-of-the-art for worldwide markets. Position Responsibilities /
Essential Functions:
Percentage Time Accountability 30% Market Authorization (assist with the following) US FDA Registrations/Listings Canada Medical Device Licenses EU product registrations Rest of World product registrations Maintain product submissions Maintain CE certification Maintain CFGs Maintain D of Cs Maintain Product Lists 30% Post-Market Surveillance Update design files, technical files, risk files, and other technical documentation based post-market surveillance data and trends. 30% Post Delivery Activities (assist with the following) CAPA and Complaint investigations and record keeping Product return coordination for complaint investigations 1 0% General Regulatory Affairs Support Inquiries and sales support activities Tender and quote reviews Customs and import/exports support activities Regulatory documentations and records management
QUALIFICATIONS
Required Qualifications:
Education:
Bachelor's degree in life sciences or other related field.
Experience:
1 - 3 years of regulatory affairs work experience with medical devices.
Skills:
Computer proficiency in Microsoft Office applications. Excellent communication skills, especially written communications. Excellent organizational and record keeping skills. Attention to detail with excellent proofreading, writing and editing skills. Good team player with a collaborative work style.
Preferred Qualifications:
Education:
Master of Science -
Regulatory Affairs Experience:
Preparing and submitting regulatory submissions.