Overview
Quality Engineer Jobs in Homestead, Florida, USA at ZipRecruiter
Job Description:
Coordinates design review meetings to review all quality aspects of new products. Interfaces with Product Development Engineers to ensure quality considerations during the concept stage.
Supports Design Control activities by ensuring compliance with FDA and international regulations.
Leads and participates in Design Failure Modes and Effects Analysis (DFMEA) and risk assessments.
Reviews protocols and participates in V&V planning to ensure alignment with product requirements.
Participates in protocol review and supports testing strategy, ensuring robust verification and validation processes.
Develops various inspection techniques and procedures to ensure product integrity to design specifications. Responsible for the writing, approval, and implementation of Incoming, In-Process, and Final Inspection procedures and operator self-inspection procedures.
Works with other Quality Engineers and the Metrology Lab personnel on the development of all product gaging.
Supports the development and review of process and equipment validation/qualification (IQ/OQ/PQ) and MSA of internal processes.
Works with suppliers, management, Engineers, and Manufacturing associates in the resolution of quality problems. Also, assists each of these groups with capability studies and the application of statistical quality control.
Interfaces with Manufacturing Engineers to review processes for new products and coordinate process validations and capability studies. Recommends process monitoring devices where applicable.
Assists with complaint investigation and documentation interfaces with Regulatory Affairs to support UL, IEC, and FDA submissions. Participates in internal audits conducted by internal employees and regulatory agencies.
Develops and executes supplier qualification processes, including supplier contracts and PPAPs.
Manages and drives timely resolution of nonconformances (NCs) and corrective & preventive actions (CAPAs).
Requirements:
Bachelor’s degree in Engineering, Quality, or a related field (Master’s preferred).
5+ years of experience in medical device quality engineering or a related field.
Strong knowledge of ISO 13485, FDA QSR (21 CFR Part 820), EU MDR, and risk management (ISO 14971).
Experience with Design Control, Process Validation, CAPA, and Supplier Quality.
Proficiency in statistical analysis tools (Minitab, JMP, Excel) and problem-solving methodologies (8D, DMAIC).
Certified Quality Engineer (CQE) or Six Sigma certification is a plus.
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Title: Quality Engineer
Company: ZipRecruiter
Location: Homestead, Florida, USA
Category: Engineering (Quality Engineering, Biomedical Engineer, Process Engineer), Quality Assurance – QA/QC (Quality Engineering)
