A Proactive Quality/Regulatory/Technical & Compliance Consultant with a broad practical & technical knowledge. Specialist expertise and knowledge within the Medical Devices industry with a wealth of experience in both Quality and Regulatory capacities
Areas of expertise:
• ISO 13485
• Technical File compilation
• Support for 510k submission
• V & V protocol approval
• MDD/ MDR
• CAPA
• NPI
• Risk Management
• Internal Auditing
• FDA audit preparation
Title: QA/RA
Availability: 24th April
Location: Birmingham
Hourly rate: Approx £85
