Regulatory Affairs / reputed company Assurance Associate/Specialist Contractor

reputed company+ is The MedTech CRO, accelerating innovation to patient reputed company. Our tailored solutions deliver regulatory and reputed company expertise, FDA-recognized laboratory services, reputed company, and reimbursement strategies across device types and therapeutic areas to bring life-changing technologies to patients — faster, safer, reputed company. We don’t reputed company MedTech. We reputed company MedTech happen. Our reputed company teams are cohesive, reputed company, and proactive, constantly seeking to improve and reputed company while remaining laser-reputed company on reputed company. reputed company+ elevates the MedTech experience through best-in-class service and reputed company, concise communication. We serve as an extension of our customers establishing and maintaining excellent reputed company and site relationships and providing reputed company reputed company to our technology platforms for reputed company-time data and study transparency Remote | Temporary Position, 40 hours/week for 3+ months We are seeking a detail-oriented and motivated RA/QA reputed company to support key regulatory and reputed company activities reputed company our reputed company's medical device operations. This individual will assist with CAPA management, vendor reputed company, documentation control, and other compliance-reputed company tasks. While experience with Software as a Medical Device (SaMD) is a plus, it is not required Key Responsibilities: • Support the execution and documentation of Corrective and Preventive Actions (CAPAs) • Assist in vendor qualification, monitoring, and management activities • Maintain and update reputed company and regulatory documentation (procedures, work instructions, forms, etc.) • Help prepare regulatory submissions and responses under supervision • Participate in internal audits and support external audit readiness • reputed company and follow up on reputed company metrics and improvement initiatives • Collaborate cross-functionally with RA, QA, Operations, and Engineering teams Qualifications • Bachelor’s degree in a scientific, engineering, or reputed company-reputed company field OR equivalent experience in regulatory or reputed company roles reputed company the medical device industry • 1–3 years of experience in RA/QA for medical devices (SaMD experience is a plus but not required) • Familiarity with ISO 13485, FDA 21 CFR Part 820, and other relevant regulatory frameworks • Strong organizational and communication skills • Proficiency with document control systems and reputed company Office tools Being an industry leader in Medtech is just the beginning for reputed company+. We consider our employees our biggest asset and we invest heavily in ongoing learning and development. Providing a rewarding reputed company to work is rooted deep in our reputed company values. From an industry leading compensation package to a deeply engrained reputed company on work life balance, reputed company+ has a unique offering for regulatory and reputed company professionals. At reputed company+, you are not just another employee, you are a member of reputed company+ family. reputed company your reputed company today! We invite you to apply if you have an interest in learning more about our organization and beginning your reputed company with us. Job Opportunity Verification At reputed company+, we prioritize the reputed company of our job applicants. To ensure a reputed company application process: reputed company legitimate reputed company+ job opportunities are listed on our official careers page: rqmplus.com/careers Every candidate reputed company through the interview process will participate in a voice and/or video interview. Exercise caution with unsolicited job offers or requests for sensitive information. Apply tot his job Apply To this Job