Quality Assurance Engineer

Boston  ‐ Onsite

Keywords

Quality Management Corrective and Preventive Action (CAPA) Medical Material Auditing Biology Regulatory Compliance Failure Mode Effects Analysis Food Safety Standard Operating Procedure Health Care ISO 13485 Manufacturing Regulatory Requirements Root Cause Analysis Manufacturing Processes Regulatory Affairs Safety Principles Risk Management

Description

We have a current opportunity for a Quality Assurance Engineer on a contract basis.

Our client is a leading innovator in the medical device industry, dedicated to improving patient outcomes through cutting-edge technology and rigorous quality standards. They are seeking a talented Quality Assurance Engineer to join their dynamic team in Massachusetts.

Job Description:

Responsibilities:
  • Develop, implement, and maintain quality assurance protocols and procedures to ensure compliance with industry standards and regulatory requirements.
  • Conduct thorough inspections and audits of manufacturing processes, ensuring adherence to quality standards.
  • Collaborate with cross-functional teams, including R&D, manufacturing, and regulatory affairs, to address quality issues and implement corrective actions.
  • Perform root cause analysis and implement corrective and preventive actions (CAPA) to resolve quality issues.
  • Participate in the design and development of new medical devices, providing quality assurance input to ensure product reliability and safety.
  • Maintain and update quality documentation, including standard operating procedures (SOPs), work instructions, and quality records.
  • Conduct training sessions for staff on quality assurance processes and best practices.
  • Stay current with industry trends and regulatory changes to ensure ongoing compliance.


Qualifications:
  • Bachelor's degree in Engineering, Life Sciences, or a related field.
  • Minimum of 3-5 years of experience in quality assurance within the medical device industry.
  • Strong knowledge of FDA regulations, ISO 13485, and other relevant quality standards.
  • Experience with quality management systems (QMS) and tools such as CAPA, FMEA, and risk management.
  • Excellent analytical and problem-solving skills.
  • Strong communication and interpersonal skills, with the ability to work effectively in a team environment.
  • Detail-oriented with a commitment to maintaining high-quality standards.
Start date
3.2025
Duration
12 months
From
Phaidon International
Published at
06.03.2025
Contact person:
Marcel Millott-Buckley
Project ID:
2855755
Industry
Manufacturing
Contract type
Freelance
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