Search the 13 jobs at RQM+

As a Regulatory Affairs Consultant, you will develop and maintain regulatory strategies to ensure compliance for advanced surgical devices while leading cross-functional teams and providing mentorship. You will manage global coordination for regulatory submissions and contribute to customer satisfaction through effective regulatory expertise.

The Quality Assurance Administrator is responsible for maintaining and improving the Quality Management System (QMS), ensuring compliance with quality standards and regulations, managing quality-related documentation, conducting audits, analyzing quality data, and supporting continuous improvement initiatives.

The Inside Sales Representative at RQM+ is responsible for growing the sales pipeline by converting inbound leads and conducting outbound outreach. They collaborate with Business Development, Marketing, and other teams to understand customer needs and provide suitable solutions while maintaining client relationships and documenting activities in CRM systems.

RQM+ focuses on regulatory and quality consulting for the medical device sector, aiming to support companies in achieving success and driving economic growth through partnerships and community engagement.

The Senior Toxicologist at RQM+ conducts toxicological risk assessments for medical devices, focusing on chemical characterization, biological evaluation, and compliance with global regulations. Responsibilities include evaluating E&L data, hazard assessments, and working with regulatory agencies. The role requires strong technical writing skills and a deep understanding of biological safety regulations.

The GCP Auditor will manage audit projects, execute audits, and prepare reports while mentoring junior auditors and identifying additional client support opportunities. Client interaction and maintaining professional integrity in challenging situations are key responsibilities.

Provide specialist knowledge and advice on IV infusion sets or IV tubing related to 510(k) requirements in a short term assignment. The role requires answering specific client questions and leveraging extensive knowledge of the medical device industry.

The Senior Manager, Quality Systems oversees the development and maintenance of quality management systems in compliance with regulatory requirements. This role involves managing document control, change control, training, and complaint management processes, fostering cross-functional collaboration, and mentoring team members.

The Project Accountant I supports the revenue generation cycle by handling invoicing, purchase orders, deposits, and cash applications. Responsibilities include billing rules assistance, revenue entry, financial inquiries handling, project financial performance monitoring, and performing special projects as assigned.

RQM+ is looking for expert personnel in areas such as Regulatory Affairs, Quality Assurance, Clinical Trials, Auditing, Medical Writing, and Laboratory services. The firm provides consulting solutions to the medical device and diagnostics industries, focusing on regulatory and quality compliance to promote economic growth and community improvement.

The Inside Sales Representative at RQM+ is responsible for growing the sales pipeline by converting inbound leads and proactively reaching out to potential clients. Responsibilities include nurturing client relationships, managing industry data for sales opportunities, and collaborating with Business Development and Marketing.

The Account Manager at RQM+ fosters client relationships while identifying growth opportunities. Responsibilities include creating growth roadmaps, achieving sales targets, conducting check-ins for client satisfaction, and collaborating with internal teams to prepare contracts and proposals. The role emphasizes proactive problem solving and maintaining strong client connections within the MedTech industry.

As an Auditor Consultant at RQM+, you will conduct supplier audits for clients in the EU and U.S., both on-site and remotely, leveraging previous FDA and regulatory experience. You will assess compliance with various regulatory standards and contribute to audit practices.