Senior Design Assurance Engineer
Brio GroupHighlight
Summary
About the Role
About You
- Bachelor's degree in Engineering or related technical field.
- 5+ years of medical device quality/design assurance experience.
- Strong knowledge of Design Controls, ISO 13485, ISO 14971, and 21 CFR Part 820.
- Experience with risk management, process validation, and statistical analysis.
- ASQ certification (CQE or CMQ-OE).
- Comfortable in fast-paced or early-stage environments.
- Strong communicator who can influence across technical teams.
"Hire Possibilities" Brio Resource Group - Your biopharmaceutical recruiting experts - is transforming the way today's most sought after "A" Talent is introduced and placed in strategic roles with desirable companies. Brio was founded by a seasoned group of professionals with over 75 years of staffing and outsourcing experience delivering results to Pharmaceutical, Biotechnology, Medical Device, CRO and Information Technology companies in North America. Our progressive approach utilizing technology, contemporary sourcing and recruitment methodology delivers successful fill rates exceeding 90%. We provide Executive Search, Contract Staffing, Project Outsourcing and Strategic Direct Placement to include the following specialties: Medical Affairs, Clinical Operations, Monitoring & Site Management, Clinical Project & Program Management, Clinical Programming & Data Management, Biostatistical Analysis & Reporting, Pharmacovigilance, Medical Writing, Regulatory Affairs, Quality Assurance, Compliance and Information Technology Staffing. We take pride being connected and partnering with today's elite emerging Biopharma companies. Our SME Executive Recruiters provide industry expertise and truly understand our candidate's specialty, needs and career objectives. We provide access to a majority of our clients' jobs on a confidential or exclusive search basis. Brio Resource Group is headquartered in Reston, VA and has a regional office in San Diego, CA. Website: www.briogrp.com