Top reasons to work for my client:
- Our client is a global medical technology company that is advancing the world of health by improving medical discovery, diagnostics and the delivery of care.
- They are one of the largest global medical technology companies in the world.
- Its 65,000 employees have a passion and commitment to help improve patient outcomes, improve the safety and efficiency
- Career advancement, well liked management
- Autonomy in the workplace
If this sounds interesting, let's talk!
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What you will be doing:
- Act as a resource to work groups and project teams, within the plant and outside the plant, regarding quality and regulatory issues.
- Lead or participate on Kaizen teams to improve quality and reduce waste.
- Investigate and provide engineering solutions to quality-related manufacturing issues.
- Maintain familiarity with manufacturing processes and products to evaluate the cause and effect of defects and identify trends in process and product quality.
- Provide technical input for projects using FMEAs, risk mitigation, plant validations, DOE experiments, and other experiments and investigations as assigned.
- Lead projects using continuous improvement tools and methodologies such as Six Sigma, Lean, and others.
- Work with all departments to maintain the highest quality standards.
- Formulate, review, and implement policies and procedures related to product quality and process control as appropriate.
- Ensure all activities comply with government regulations (OSHA, EPA, FDA, ISO, etc.) and corresponding company policies/procedures, including activities and programs defined in the Quality Systems Manual for Broken Bow.
- Coordinate machine and process capability studies, analyze the data, and submit recommendations.
- Design and assist Production, Engineering, and the Division in completing new product/process evaluations, including Hazard Analysis.
- Coordinate communication between Division R&D and plant personnel on new products, product improvements, and product issues.
- Participate in Engineering and Production functions as required to achieve the overall objectives of the plant.
- Perform other duties as assigned, such as Internal Audits and PIR/CFI investigations.
- Support plant safety initiatives.
Experience you will need:
- BA/BS degree in Science, Engineering, or a related discipline.
- Medical device manufacturing experience preferred.
- Preferred 1–2 years of relevant experience; however, internships, co-op experience, and relevant engineering projects will also be considered.
- Strong communication and interpersonal skills, with the ability to work effectively across diverse teams.
- Flexible and adaptable, with the ability to support a variety of day-to-day responsibilities.
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