burtandassociates

Project Manager — Design Control Remediation Program Medical Device | ISO 13485 / EU MDR | 1099 Independent Contractor Engagement Type: 1099 Independent Contractor Schedule: Part-time, 20–24 hours per week Duration: 12 months, with potential extension Location: Remote (U.S.) Travel: Up to one week p

About the Role MB&A is seeking a hands-on Principal Regulatory Consultant who combines recent, real-world regulatory submission experience with practical Quality Engineering execution. This role is designed for consultants who actively prepare and submit filings, engage directly with regulatory auth

About the Role MB&A is expanding its network of high-impact consultants to support strategic quality and project leadership initiatives for leading med-tech and life sciences companies. We are seeking senior Quality Engineers who bring executive-level project leadership, strong stakeholder presence,

This is a generic posting to allow consultants seeking new opportunities to submit their resume for consideration. We are constantly seeking more Medical Device Quality Auditors, Engineers and Quality Systems Specialists. We also need various Operations, PMO, and Engineering associates to staff manu

The Validation Engineer – Olive Branch will play a pivotal role in overseeing and optimizing all aspects of our Olive Branch Validation programs. The position is responsible for process development, maintenance and risk mitigation while ensuring execution of deliverables, communication and fostering