
Quality Engineer 3
- Londonderry, NH
- $83,000-129,000 per year
- Permanent
- Full-time
- In-depth knowledge of ISO 13485, FDA regulations, EU MDR/IVDR, and cGMP requirements.
- Expertise in risk management principles, including ISO 14971 and Process Failure Mode and Effects Analyses (PFMEAs).
- Advanced understanding of statistical tools, including Six Sigma, Statistical Process Control (SPC), and Design of Experiments (DOE).
- Strong familiarity with Quality Management Systems (QMS) and compliance activities.
- Knowledge of lean manufacturing principles and operational excellence practices.
- Proven ability to lead root cause investigations, manage Nonconforming Events (NCEs), and implement effective CAPAs.
- Proficiency in analyzing quality system metrics and product quality data to identify trends and initiate corrective actions.
- Expertise in authoring, reviewing, and approving technical reports for Test Method Validations and Process Validations (IQ, OQ, PQ).
- Strong technical writing and communication skills for compliance documentation and stakeholder communication.
- Leadership and mentorship skills to guide and develop junior engineers.
- Effective collaboration and partnership-building skills to work cross-functionally across teams.
- Ability to manage seamless design transfers to production and product transfers between manufacturing sites.
- Lead with ownership, integrity, and accountability, taking responsibility for outcomes and driving results.
- Act with urgency and maintain a bias toward action, ensuring timely communication and updates.
- Foster strong partnerships and teamwork, investing in relationships with stakeholders to achieve shared goals.
- Delight customers by exceeding expectations and delivering innovative solutions.
- Embrace a continuous improvement mindset, actively seeking opportunities to optimize processes and celebrate wins as a team.
- Commit to compliance, safety, and environmental sustainability while supporting a positive and inclusive work environment.
- 7+ years of experience as a Quality Professional in the medical device industry or equivalent combination of education and experience.
- Proven experience with ISO standards, FDA regulations, and Quality Management Systems.
- Demonstrated success in leading CAPA teams, driving investigations, and implementing sustainable corrective actions.
- Experience in managing design transfers, production processes, and product transfers while maintaining compliance.
- Hands-on experience with statistical tools and lean manufacturing principles to improve process capability.
- ASQ Certified Quality Engineer (CQE) certificate and/or Six Sigma Certification preferred.