Senior Quality Control Engineer

Biomerics-posted about 3 hours ago
Full-time • Mid Level
Monroe, CT
1,001-5,000 employees
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The Senior Quality Engineer will play an important role within the Biomerics Extrusion, Metals, and Plastics team, providing Quality Engineering leadership in developing, establishing, and maintaining Quality Engineering methodologies, systems, and practices, which meet internal, customer, and regulatory requirements.

  • Participate in Product Development teams, providing Quality input and support
  • Develop and implement Control Plans, Master Validation Plans, and Inspection Procedures
  • Develop validation strategies, ensuring all applicable requirements are met from planning, protocol definition, leading execution of protocols, analyzing and reporting results, and completing report and gaining necessary approvals to close
  • Leading the development and results analysis of validation plans (IQ/OQ/PQ), Test Method Validation (TMV), Gage R&R, and test protocols to qualify and validate existing product designs, processes, and equipment
  • Determine and recommend sampling plans, equipment requirements, measurement techniques, and training requirements that will ensure specific quality levels
  • Support new product introductions and process changes
  • Support Manufacturing Engineering in the creation, release, and maintenance of DHR, Bill of Materials, and manufacturing specifications
  • Review and approve product documentation
  • Leads preparation of risk management files and reports for product releases, and has primary responsibility for risk management activities from product conception through commercialization
  • Ensure risk management processes are followed and documented
  • Ensure compliance to Biomerics quality standards, policies, and procedures
  • Support external customer and regulatory agency audits
  • Maintain consistent dialogue with customers and teammates to ensure clear communication and expectations
  • Lead investigations for nonconformances and customer complaints
  • Utilize problem solving tools to analyze and identify root causes and implement corrective actions
  • Identify opportunities for process improvement and implement solutions
  • Monitor quality performance metrics and trends
  • Provide leadership and mentoring to other Quality team members
  • Promote a culture of quality and foster a culture of compliance and continuous improvement
  • Bachelor's degree in Engineering, Quality, or a related field or equivalent experience
  • 5+ years of experience in Quality Engineering within a medical device manufacturing environment
  • Working knowledge of process development and validation
  • Strong knowledge of Quality Systems and regulations (e.g., FDA QSRs, ISO 13485, ISO 14971).
  • Experience with root cause analysis, CAPA, and risk management.
  • Familiarity with statistical tools and methods.
  • Knowledge of medical device manufacturing processes.
  • Strong problem-solving and analytical skills
  • Excellent communication and interpersonal skills
  • Proficiency in Microsoft Office and Minitab
  • Ability to work independently and as part of a team
  • Strong organizational and project management skills
  • ASQ certifications (e.g., CQE, CQA) are preferred
  • Medical/Dental/Vision Insurance
  • Short-Term Disability
  • Long-Term Disability
  • Life Insurance
  • Paid Vacation Days
  • Paid Holidays
  • 401k
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