NOW HIRING: Data Analyst - REMOTE

Data Management Specialist – IVDR (EUDAMED) – MUST have exp with Gathering & consolidating regulatory data related to IVDR Device registrations. Bach degree 1-3 years exp level Seeking a Data Management Specialist to support our Regulatory Affairs and Quality teams in the context of the EU In Vitro Diagnostic Regulation (IVDR). The successful candidate will be responsible for collecting, organizing, and entering regulatory data related to medical device registrations, and other associated attributes into our Product Data Management System. This role may also include performing system validation testing and drafting Standard Operating Procedures (SOPs) to ensure the sustainable maintenance and accuracy of these data over time How You'll Make An Impact: Gather and consolidate regulatory data related to IVDR device registrations from internal and external sources. Enter and maintain data in the company’s product data management tool, ensuring completeness, accuracy, and compliance with internal standards. Develop and document Standard Operating Procedures (SOPs) and work instructions to support long-term data integrity and consistency. Collaborate with cross-functional teams (Regulatory Affairs, Quality, R&D, Supply Chain) to ensure data alignment and traceability. Support continuous improvement initiatives for data quality and process efficiency. What You Bring: Bachelor’s degree (or equivalent) in Life Sciences, Quality Management, Regulatory Affairs, or related field. 1-2 years of experience in the medical devices or IVD industry is highly preferred. Strong attention to detail and commitment to accuracy and data integrity. Excellent organizational and analytical skills. Strong appreciation for the role of high-quality data in ensuring patient safety and regulatory compliance. Clear written and verbal communication skills in English. Proficiency in Microsoft Word, Excel. #GRPA Job Type: Contract Pay: $36.00 - $39.00 per hour Expected hours: 40 per week Work Location: In person