Quality Engineer I

Resonetics; New Chicago (OH); On-site; USD 54,000 - 84,000; Full time

Job summary

Resonetics is seeking a Quality Engineer I in New Chicago, Ohio to apply Quality Engineering techniques in the medical device industry. The role involved planning projects and ensuring adherence to regulations and industry standards.

Ideal candidates will have experience in a manufacturing environment and a relevant degree. This position offers a competitive salary range of $54,000–$84,000 based on experience and qualifications, fostering a culture of innovation and collaboration.

Qualifications

• 1-2+ years' experience in Quality Engineering in a Manufacturing environment.
• Ability to create job-related documentation for quality purposes.
• Knowledge of Statistical software and Minitab.

Responsibilities

• Apply Quality Engineering methods to daily tasks.
• Conduct root cause investigations and assess corrective actions.
• Develop and maintain Quality control plans according to product risk.

Skills

Quality Engineering

Problem-solving techniques

Statistical software

Technical writing

Communication skills

Education

Bachelor's degree or equivalent experience

Tools

Minitab

ISO 13485 standards

Job description

Overview

Resonetics is a global leader in advanced engineering, prototyping, product development, and micro manufacturing, driving innovation in the medical device industry. With rapid expansion across all our locations, we continue to push the boundaries of technology while fostering a dynamic, employee-centered culture. Our commitment to excellence and continuous improvement makes Resonetics an exciting place for professionals passionate about shaping the future of micro-manufacturing and being part of something bigger.

We are looking for a Quality Engineer I to join our growing team in Kettering, OH. This role applies Quality Engineering and scientific method techniques and principles to daily tasks and activities; applies relevant regulations, standards, and industry best practices to assignments; plans and conducts projects and assignments with moderate to high technical responsibility, complexity or strategic input; receives summarized instructions from technical Quality leaders at various levels in addition to other functional stakeholders.

Join Resonetics and be part of a team that’s redefining medical device manufacturing. If you’re passionate about innovation and thrive in a fast-paced environment, we’d love to hear from you.

Responsibilities

• Demonstrates proficiency in applying various tools and methods to identify and realize new product or process introductions (ex. QMS, product related), and business improvements.
• Contributes to the application of various risk management and risk mitigation tools and practices.
• Leads and/or contributes to root cause investigations using various problem-solving techniques and tools and assesses effectiveness of corrective actions.
• Conducts and supports the development of test methods in equipment, process, and product qualifications/validations.
• Develops, implements, and/or maintains process Quality control plans are in accordance with product risk level and are followed.
• Develops, implements and/or maintains process controls using appropriate techniques and tools (ex. Statistical process controls, statistical inspection sampling).
• Supports all levels of Design Controls per ISO 13485.
• Participates in design/technical reviews as appropriate.
• Lead QE on product development projects.
• Interprets standard and non-standard sampling plans.
• May act as a subject matter expert (SME) in at least one routine Quality area.
• Liaising with customer quality personnel to resolve issues and Customer Complaints.
• Generating process deviations, Customer Change Notices, validation protocols & reports.
• Assisting with troubleshooting of production and product development processes.
• Developing and maintaining quality/control plans.
• Ensuring Quality Management Systems procedures and appropriate regulations and industry standards are being utilized throughout the product development and process development processes.
• Developing Risk documentation in compliance with the QMS and regulatory standards, such as PFMECAs.
• Conducting Gage R&R studies.
• Resolving Corrective and Preventive Actions.
• Developing Quality Procedures and conducting training to all personnel as appropriate.
• Approving Nonconformance disposition.
• Analyzing production and validation data.
• Working on continual improvement and process assessment projects as assigned.
• Author protocols or provides support in performing qualification validation protocols in support of design control deliverables.
• Support Equipment Calibration and Maintenance per the applicable procedures.

Required Qualifications

• 1-2+ years’ experience in a Quality Engineering role in Manufacturing environment with preference in experience with Medical Device or regulated environment.
• Ability to create job-related documentation for quality purposes.
• Familiarity with ISO 13485 standards or working in regulated environment.
• Demonstrated technical writing and communication skills.
• Working knowledge of Statistical software and/or Minitab.
• Bachelor’s degree or equivalent experience.

Preferred Qualifications

• Experience with automated or manual inspection equipment
• Familiarity with ISO Quality Systems particularly in medical device manufacturing.
• Use of optical inspection equipment. This may be defined as a magnifier, microscope, and/or equipment used for measuring capacity.

Physical Demands

• Light office work only; position may include up to 10% domestic and international travel.
• Standing and walking for short periods of time.
• Ability to use a microscope, including manipulating small objects under a microscope.

Compensation

The compensation for this role is competitive and will be based on experience and qualifications. The anticipated range is $54,000–$84,000.

For temp, temp-to-hire, and regular full-time positions, our company policy is that we are unable to provide visa sponsorship. Candidates must already be legally authorized to work in the United States without the need for sponsorship now or in the future.