Quality Engineer

JVT Advisors; Bethel (CT); On-site; USD 90,000 - 120,000; Full time

Job summary

JVT Advisors in Bethel, CT is seeking a Quality Engineer III to apply advanced quality engineering methods to daily tasks and to lead risk management across product development and manufacturing processes. The role focuses on regulatory compliance with ISO 13485 and FDA 21 CFR 820, mentor colleagues, and drive continuous improvement while collaborating with customers and suppliers to resolve issues.

The position is full-time, on-site in Bethel, offering day-one benefits and opportunities to

Qualifications

• Must create job-related quality documentation.
• Familiar with ISO 13485 and FDA 21 CFR 820.
• Min 2 years in quality engineering for medical devices or equivalent.
• Strong technical writing and communication skills.
• Experience with statistical software (Minitab) or similar.
• Bachelor’s degree or equivalent experience.
• Interact with customers and suppliers; audits may be required.

Responsibilities

• Apply advanced quality engineering methods to tasks and projects.
• Lead risk management tools and practices.
• Conduct root cause investigations and verify corrective actions.
• Develop test methods for equipment, processes, and products.
• Maintain quality control plans aligned with risk levels.
• Implement statistical process controls and sampling plans.
• Ensure ISO 13485 and FDA 21 CFR 820 compliance.
• Lead QE on product development and continuous improvement.
• Mentor others in quality capabilities.
• Collaborate with customer quality personnel to resolve issues.
• Assist with troubleshooting production processes.
• Provide support for validation protocols.

Skills

Technical writing

Statistical analysis

Documentation

Education

Bachelor’s degree or equivalent experience

Tools

Minitab

Job description

Full-time Quality Engineer needed in Bethel, CT, excellent benefits day one

Summary

This Quality Engineer III applies advanced Quality Engineering and scientific method techniques and principles to daily tasks and activities; applies relevant regulations, standards, and industry best practices to assignments; plans and conducts projects and assignments/activities with moderate to high technical responsibility, complexity or strategic input; Acts as a subject matter expert in routine Quality Engineering and scientific matters; receives occasional, summarized instructions from technical Quality leaders at various levels in addition to other functional stakeholders.

Responsibilities

• Demonstrates high level of proficiency in applying various tools and methods to identify and realize new products or process introductions (ex. QMS, product related), and business improvements.
• Leads and contributes to the application of, and/or develops innovative applications for various risk management and risk mitigation tools and practices.
• Leads and/or contributes to root cause investigations using various problem-solving techniques and tools and assesses effectiveness of corrective actions.
• Leads, conducts and supports the development of test methods in equipment, process, and product qualifications/validations.
• Develops, implements, and/or maintains process Quality control plans in accordance with product utilization and risk level and ensures they are followed.
• Develops, reviews, implements and/or maintains process controls using appropriate techniques and tools (ex. statistical process controls, statistical inspection sampling).
• Support and ensure all levels of regulatory requirements per ISO 13485:2016 and FDA 21 CFR 820 are being utilized, in addition to other product regulatory requirements.
• Leads or participates in design/technical reviews as appropriate.
• Lead QE on product development, sustaining and continuous improvement projects.
• Interprets and implements standard and non-standard sampling plans.
• Act as a subject matter expert (SME) in at least 2 routine Quality areas.
• Partners with senior technical leaders (internal and external to the organization) to develop innovative approaches for identifying technical opportunities and quality improvements.
• Mentors and teaches others in various technical capabilities.
• Liaising with customer quality personnel to resolve issues and Customer Complaints.
• Assisting with troubleshooting of production processes
• Assisting with production and product development processes.
• Leading development of metrology equipment.
• Developing and maintaining quality/control plans.
• Ensuring Quality Management Systems procedures and appropriate regulations and industry standards are being utilized throughout the product development and process development processes.
• Developing Risk documentation in compliance with the QMS and regulatory standards, such as PFMEAs.
• Resolving Corrective and Preventive Actions
• Developing Quality Procedures and conducting training to all personnel as appropriate
• Approving Nonconformance disposition
• Analyzing production and validation data
• Working on continual improvement and process assessment projects as assigned
• Provides support or authors validation protocols for manufacturing and quality deliverables. Serves as the quality representative for Lightspeed projects, ensuring alignment with quality standards, risk mitigation, and process capability objectives.
• Support Equipment Calibration and Maintenance per applicable procedures.

Required Qualifications

• Ability to create job-related documentation for quality purposes.
• Familiarity with ISO 13485 standards and FDA 21 CFR 820 regulations.
• Minimum 2 years’ experience in a Quality Engineering role for a medical device manufacturer and/or start-up company, or equivalent engineering experience.
• Demonstrated technical writing and communication skills.
• Working knowledge of Statistical software and/or Minitab.
• Bachelor’s degree or equivalent experience.
• Interact with customer and supplier companies in a professional manner; proactively communicate with them to ensure an ongoing two-way exchange of information. Auditing and qualification of new suppliers may be required.

Preferred Qualifications

• CQE and/or Six Sigma Green or Black belt
• Strong attention to detail and satisfactory organizational skills
• Able to self-manage project tasks

Physical Demands

Standing and walking for short periods of time

Ability to use a microscope, including manipulating small objects under a microscope