Overview
Quality Engineer Jobs in Dover, NH at Lumicity
Title: Quality Engineer
Company: Lumicity
Location: Dover, NH
Position Responsibilities:
Quality Control: Develop manufacturing processes and process controls for in-house and supplier processes. Lead processes related to the receiving and inspection of components, management of inventory, and device assembly builds. Support inspections of incoming materials, in-process components, and finished products to ensure compliance with design requirements.
Design Assurance: Lead quality engineering activities related to product development of the ReValve devices. This will include working with a cross-functional team on defining design inputs/outputs, developing design verification test protocols/reports, performing risk management, supplier development, test methods, and defining inspection criteria.
Risk Management: Participate in risk management activities for early product development to proactively identify potential issues, define requirements, and monitor quality related issues.
Quality Management System: Drive adherence of processes to defined quality management system procedures. Ensure internal quality systems meet required quality standards with a focus on continuous improvement.
Regulatory Compliance: Maintain compliance with regulatory requirements (e.g., FDA, ISO 13485) and company quality standards, ensuring adherence to Good Manufacturing Practices (GMP).
Equipment Calibration & Maintenance: Support the calibration, maintenance, and qualification of testing and production equipment for compliance with relevant standards.
Documentation: Prepare and maintain detailed and well-organized design history file, device master record, and device history record documentation. Lead the completion of technical summaries, inspection reports, non-conformance reports (NCRs), device investigations, and quality records. Ensure proper documentation of test results, test protocols, reports, and associated documentation for both design history and device history files.
Qualifications:
· Bachelor’s degree in engineering, science, or technical discipline required with 2+ years of quality systems experience.
· Experience in quality control, design assurance, or related functions, preferably within the medical device industry.
· Strict attention to detail, with strong problem-solving abilities.
· Strong analytical skills with the ability to identify issues and interpret complex data.
· Ability to manage competing priorities in a fast-paced environment
· Demonstrated ability to work effectively in cross-functional teams and collaborate with manufacturing, engineering, and regulatory departments.
· Hands-on approach with a learning mindset
· In-depth knowledge of FDA regulations, ISO 13485, GMP, and other relevant standards.
