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Fresenius Medical Care

Operates dialysis facilities and renal care

Design Quality Assurance Expert

Biomedical Engineering & Medical DevicesConfirmed live in the last 24 hours
Full-timeSuzhou, Jiangsu, ChinaNo salary listedHybrid

About the Job

Requirements

  • At least 10 years of medical device experience is desirable.
  • Advanced knowledge of medical device regulations, including NMPA regulation, MDD 93/42/EEC, MDR 745/2017, and MDSAP.
  • Advanced knowledge of applicable quality management and risk management standards, including ISO 13485, ISO 14971, ICH Q10, EU GMP, and FDA 21 CFR §820.250.
  • Knowledge of internal and external processes and structures and corporate Quality Management requirements.
  • Knowledge of CAPA methodology.
  • Basic knowledge of statistical methods.
  • Ability to manage stakeholders and communicate effectively.
  • Ability to balance business needs with product quality and regulatory requirements.
  • Ability to serve as a trusted quality partner in cross-functional project meetings.
  • Ability to lead cross-functional local design quality aspects while maintaining connections with global teams.

Responsibilities

  • Ensure design quality compliance of medical device design and development activities throughout the product lifecycle.
  • Act as the Design Quality representative within cross-functional project teams, providing oversight of design controls, design transfer, and design change activities in accordance with applicable regulations, standards, and internal procedures.
  • Ensure design and development activities comply with regulatory, quality, and design control requirements.
  • Represent Design Quality in product development, design transfer, and design change projects.
  • Review and approve design control deliverables, Design History File documentation, and project milestones.
  • Support preparation of documentation required for regulatory submissions and technical files.
  • Participate in Design Reviews, Phase Exit Reviews, and compliance assessments.
  • Provide training and guidance on design control and quality requirements.
  • Review and approve Design & Development-related nonconformances, CAPAs, and change controls.
  • Conduct audits and compliance checks to ensure adherence to the Quality Management System.
  • Support design transfer activities and collaboration between R&D, Regulatory Affairs, and Manufacturing.

Desired Qualifications

  • At least 10 years of medical device experience.

About the Company

Fresenius Medical Care

Operates dialysis facilities and renal care

Fresenius Medical Care North America provides renal care through a network of dialysis facilities and outpatient cardiac and vascular labs that deliver coordinated treatment for chronically ill patients. It also offers specialty pharmacy and laboratory services and manufactures and distributes dialysis equipment, disposables, and renal medicines. The company stands out by being the world’s largest fully integrated renal care provider with an extensive network that covers care delivery, drug and lab services, and product supply. Its goal is to ensure access to comprehensive, high-quality care for people with kidney and other chronic conditions across North America.

Company size
11-50
Company stage
Late Stage VC
Total funding
$40.2M
Headquarters
Waltham, MA
Founded
1996

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