Product Quality Engineer II

4 days ago

Burlington, Massachusetts, United States Conformis Inc Full time $85,000 - $110,000 per year


Job Summary:

The Product Quality Engineer II will be responsible for quality assurance activities including product quality engineering, non-conforming material report write ups and investigation, statistical process control, process improvements, and quality control oversight.

Essential Duties and Responsibilities:

  • Develop and maintain strong internal working relationships across Conformis.
  • Understand the objectives, responsibilities, and mission of the Quality department and work towards those goals.
  • Prioritize and plan work activities; adapt for changing conditions.
  • Assist in maintaining the quality system in accordance with applicable regulatory requirements.
  • Identify quality system process improvements and implement solutions.
  • Lead or assist with the Corrective Action/Preventive Action (CAPA) program.
  • Lead or assist with the Customer Complaint system by performing complaint investigations, including root cause analysis.
  • Assist with product inspections as needed.
  • Perform Internal Quality Audits of the quality system
  • Participate in supplier selection and approval process, including leading supplier audits and review of quality data. 
  • Perform investigations of non-conformances and drive corrective actions.
  • Participate on cross-functional product development teams.
  • Participate in product/process validations.
  • Perform risk assessments, gathering cross-functional team input.
  • Employ statistical techniques and rationale in decision-making activities driven to support non-conformance trending, CAPA effectiveness, part qualification, and process monitoring.
  • Establish and trend quality metrics and data.
  • Participate in third party audits against ISO 13485 and FDA 21 CFR Part 820 requirements.
  • Other responsibilities as assigned.

Qualifications:

  • Bachelor of Science in Engineering, Science, or Biomedical. 
  • 2+ years of Quality Assurance/Quality Engineering experience in the medical device industry and/or experience in an FDA regulated environment is required.
  • Knowledge of FDA 21 CFR Part 820 and ISO 13485, preferred.
  • ASQ certification (Certified Quality Engineer, Certified Quality Auditor, Certified Biomedical Auditor) a plus.

Skills, Abilities, Competencies Required:

  • Excellent written and verbal communication skills.
  • Able to work accurately in a fast-paced, hectic, ever-changing environment with strong attention to detail.
  • Demonstrated ability to monitor own work to ensure quality, accuracy, and thoroughness.
  • Strong organizational, analytical, and time-management skills.
  • Able to self-motivate and work both independently and as part of a team.
  • Must have a solid knowledge of Microsoft office.
  • Must be able to work in a team environment, execute responsibilities with minimal direct supervision, and have a high attention to detail.
  • Demonstrated proficiency with FDA and ISO standards for Medical Devices.

restor3d is an Equal Opportunity Employer

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