Job Description
Job Description
About the Role
We are seeking a driven and detail-oriented Quality Engineer II to join our team. This role plays a key part in ensuring our products and processes meet the highest standards of quality, safety, and compliance . You will be engaged in technical quality activities, continuous improvement projects, and cross-functional collaboration, helping to deliver goods and services that meet our customers’ expectations for quality, quantity, and timeliness .
If you are looking for an opportunity to grow your career, bring your expertise to the next level, and make a direct impact on product quality and patient safety, this position may be a great fit.
Key Responsibilities
- Enforce and support the Quality Management System and applicable SOPs.
- Perform, review, and approve testing and inspection activities, including training quality inspectors and technicians.
- Develop and implement solutions that streamline and improve quality processes .
- Support calibration and preventative maintenance of gauges and equipment.
- Optimize inspection methods, sampling plans, and documentation processes.
- Review and approve manufacturing documentation and engineering changes to ensure compliance and proper justification.
- Support production inspections, evaluate nonconforming parts, and complete nonconformance reports.
- Partner with process owners to resolve nonconformances and drive corrective and preventive action (CAPA) activities.
- Author and execute validation protocols and reports, including process, software, and test method validations.
- Support and participate in internal, external, and supplier audits as well as follow-up actions.
- Review and approve sterilization cycle results and support cycle validations where applicable.
- Leverage ERP systems to drive quality improvements and efficiencies.
- Provide overall quality and production support to meet business objectives.
- Monitor and report on quality trends and performance indicators.
Qualifications & Skills
Education : BS in Engineering or equivalent experience.Experience :Minimum 3 years of experience in Quality Engineering for medical devices or 5+ years in quality roles overall.
Knowledge of ISO-13485 and FDA 21 CFR Part 820 cGMP standards.Quality assessment and audit experience preferred.Technical Skills :Strong knowledge of disposable medical device testing, validation protocols, and report writing.
Experience with statistics, including SPC and design of experiments.Proficiency in Microsoft Office or equivalent software.Other Skills :Excellent communication (written and verbal).
Strong analytical and problem-solving abilities.Six Sigma Green Belt certification desired.Why Join Us?
Be part of a mission-driven team working to ensure safe and effective medical devices reach patients.Enjoy opportunities to lead and participate in continuous improvement projects that directly impact operations.Collaborate with talented colleagues in a supportive, growth-focused environment .Competitive compensation and benefits designed to support both your career and personal goals.Apply Today
If you are passionate about quality, eager to bring new ideas, and ready to make an impact, we invite you to apply and join our team as a Quality Engineer II .