Quality Engineer

Innovative Health LLC; Scottsdale (AZ); On-site; USD 75,000 - 98,000; Full time

Job summary

Innovative Health LLC seeks a Quality Engineer to ensure FDA/ISO compliance during process development and manufacturing of medical device components. The role improves quality, regulatory compliance, and business efficiency within the Quality Organization.

Responsibilities include CAPA monitoring, calibration maintenance, and supporting new product development with rigorous testing and documentation. Strong data analysis and cross-functional collaboration are essential.

Qualifications

• Bachelor's degree in a technical field and at least 3 years of experience in quality for medical devices.
• Knowledge of QMS requirements and regulatory standards including FDA and ISO.
• Ability to work in a fast-paced, collaborative team environment.
• Ability to coordinate cross-functional teams and communicate effectively with management and vendors.

Responsibilities

• Supports CAPA program by monitoring investigations and implementing actions.
• Maintains Calibration and Preventative Maintenance systems.
• Represents quality support for new product development initiatives.
• Verifies and validates design/process using IQ/OQ/PQ methods.
• Develops and writes test methods and documentation.
• Prepares formal test protocols and reports for manufacturing and QC.

Skills

QA/QMS knowledge

Effective communication

Training

Problem solving

Self-motivated

Education

Bachelor's degree in technical field (Bioengineering, Electrical, Mechanical)

Tools

Minitab

Microsoft Office (Word, Excel, PowerPoint, Project)

Job description

The Quality Engineer will ensure compliance to required standards including FDA and ISO during process development and the manufacturing of medical device components. In addition, this person will have responsibility for identifying and driving improvements related to quality, compliance to regulatory requirements and business efficiencies within the Quality Organization.

• Supports the Corrective and Preventive Actions Program by monitoring the system and completing investigations and implementing actions as applicable.
• Supports Calibration and Preventative Maintenance systems
• Represents and provides quality support for new product development initiatives.
• Verifies and validates design and processes utilizing IQ, OQ, and PQ process.
• Develops and writes test methods.
• Creates documentation for manufacturing, quality control, and final release processes.
• Generates formal test protocols and reports.
• Supports continuous process improvements through detailed data analysis.
• Provides documentation and support for the submission of FDA 510Ks.
• Participates in risk management activities for product and process design projects including PFMEA risk assessments.
• Reviews and approves complaint investigations.
• Conduct data analysis using Minitab or equivalent statistical software.
• Train manufacturing/QC personnel as needed on test methods or manufacturing processes.
• Document test results per GDP, ISO and FDA requirements.
• Participates in process improvement projects to reduce costs.
• Assists with environmental monitoring of production facilities and equipment.
• All other duties, as assigned.

Education and Qualifications:

• Minimum of Bachelor\'s degree in technical field (i.e. Bioengineering, Electrical Engineering, Mechanical Engineering or other technical field) and minimum of three (3) years experience.
• Ability to work in a fast paced, collaborative team environment
• Ability to handle multiple projects and coordinate cross functional teams
• Ability to communicate effectively with management, peers and external vendors
• Knowledge of Medical Device QMS requirements and regulatory requirements including but not limited to FDA CFR 21 820 and ISO 13485.
• Knowledge of risk management and risk analysis methods
• Ability to write technical documents (procedures, test methods, protocols and reports)
• Ability to conduct data analysis using Minitab
• Ability to recommend technical solutions
• Ability to specify requirements for products and equipment
• Ability to train other engineers/manufacturing/QC/technicians
• Ability to work with little supervision
• Ability to use personal computers including software such as: Word, PowerPoint, Excel, Project and Minitab
• Self-starter and highly motivated