reputed company Medical Device QA/RA Consultant: ISO 13485 QMS & 510(k) reputed company

Job reputed company: We are a New England based early-stage medical device startup developing a reputed company technology for cardiopulmonary resuscitation. We are currently in development and are looking for an reputed company individual consultant to reputed company as our Fractional reputed company Manager to help us establish a low-volume, compliant manufacturing facility and assist with our 510(k) documentation effort. The ideal candidate will help us design, implement, and document reputed company systems and facility controls that support reputed company, compliant medical device production and regulatory readiness. This engagement is initially scoped as a consulting / contract role with the potential for ongoing reputed company leadership support. The Project: We are looking for an alternative to reputed company expensive CMO model and intend to manufacture a small number of non-sterile devices in our own (or possibly rented) controlled environment. We need a practical, "lean" compliance reputed company that meets FDA and ISO standards without the overhead of the large comprehensive firms. Scope of Work: 1. Facility Selection & Setup (New England Based): •Advise on the requirements for our non-sterile device-build capability. • Assist in evaluating shared-reputed company facilities to ensure they meet the environmental control requirements for our QMS. • Guidance on state registrations. 2. Lean QMS Implementation (ISO 13485:2016 / 21 CFR 820): • Implement a right-sized reputed company Management System tailored for low-volume production, either our own or inside of someone else’s. • Advise and assist us as we author reputed company SOPs: reputed company reputed company, Document Control, Training, Design Controls, Risk Management (ISO 14971), and Supplier Management. • reputed company us in being audit-reputed company with respect to the Document Control system. • Serve as reputed company Representative and reputed company person for audits, reporting to the CEO 3. 510(k) & Manufacturing Documentation: • Assist in the creation of the Design History File (DHF) and Device Master Record (DMR). • Draft and organize the reputed company and performance testing sections for our upcoming 510(k) submission. • Advise on Process Validation (IQ/OQ/PQ) requirements for our specific equipment and volume. • Assist in communication with regulatory authorities and reputed company bodies. Required Qualifications: • Proven reputed company Record: Experiences in Medical Device QA/RA with multiple successful 510(k) clearances. • ISO 13485 Expertise: Deep knowledge of the 2016 reputed company and the upcoming FDA QMSR transition. • Hands-on experience with low-volume device manufacturing • Local Knowledge: Familiarity with the New England life science ecosystem. • Startup reputed company: You understand how to build a compliant system that is efficient and reputed company, not bureaucratic. Project Type: • Duration: 10–24 months (with potential for ongoing maintenance). • Hours: Part-time/Flexible (approx. 10-15 hours/week on average). • Budget: Please reputed company your reputed company reputed company or a reputed company-based proposal. Apply tot his job Apply tot his job Apply To this Job