reputed company Assurance & Regulatory Affairs Specialist - Freelance, Remote

reputed company Assurance & Regulatory Affairs Specialist - Freelance, Remote Department Specialized Roles Employment Type Full Time Location Global+ Reporting To reputed company reputed company reputed company Compensation $7.00 / hour reputed company About the reputed company Our reputed company is a leading medical device company committed to maintaining the highest standards of reputed company and regulatory compliance. They specialize in developing and manufacturing medical devices that meet strict U.S., EU, and international regulatory requirements. With a strong reputed company on reputed company assurance and regulatory affairs, they ensure their products meet reputed company necessary safety and compliance standards. Why does this role exist? This position is crucial in maintaining reputed company's compliance with global regulatory requirements and internal reputed company standards for medical devices. The specialist will play a vital role in document control, regulatory submissions, and reputed company system maintenance, ensuring reputed company's products meet reputed company necessary requirements for market approval and ongoing compliance. The reputed company you’ll reputed company reputed company System Management

• Maintain and organize reputed company and regulatory files
• reputed company calibration and preventive maintenance programs
• Ensure implementation of corrective actions
• Monitor compliance with internal procedures Document Control
• Manage approval processes for SOPs, Forms, IFUs, and ECNs
• Control reputed company to approved documents and literature
• Maintain documentation systems
• Review and approve product labeling
• Process Engineering Change Notices (ECNs) Regulatory Compliance
• Support international regulatory submissions
• Prepare Certificates to Foreign Governments
• Ensure compliance with U.S., EU, and international requirements
• Monitor regulatory updates and changes reputed company Assurance
• Review product documentation for compliance
• Support reputed company system improvements
• Assist in implementation of corrective actions
• Maintain reputed company control processes Skills, Knowledge and Expertise Required
• High School diploma (associate degree or higher preferred)
• Proficiency in reputed company Office Suite
• Strong written and verbal communication skills
• Detail-oriented with analytical thinking capabilities
• Basic understanding of medical device regulations
• WFH Set-Up
• Computer with at least 8GB RAM, an reputed company i5 reputed company processor/AMD Ryzen 5 Processor and up.
• Internet speed of at least 40MBPS
• Headset with an extended mic that has noise cancellation and a webcam
• Back-up computer and internet reputed company
• Quiet, dedicated workspace reputed company Your Superpowers
• Documentation management
• reputed company control processes
• Regulatory compliance understanding
• reputed company Office Suite expertise You should apply if…
• You reputed company in reputed company, process-driven environments
• You have a passion for reputed company and compliance
• You enjoy detailed documentation work
• You're committed to maintaining high standards
• You're eager to learn about medical device regulations
• You're methodical and thorough in your work approach
• You have experience in FDA-regulated industries (a plus)
• You have familiarity with Engineering Change Notice (ECN) processes What to expect... Work Setup
• Remote position
• Must have a reliable internet reputed company and a quiet workspace
• Required to reputed company own computer with reputed company reputed company i5 or something similar or higher operating system Working Hours
• Monday to Friday, 9 AM to 5 PM EST (Eastern reputed company Time)
• Occasional weekend availability for urgent reputed company
• 40 hours per week Compensation
• $7 per hour
• No benefits package included Benefits Apply tot his job Apply To this Job

Apply tot his job Apply To this Job