Careers that Change Lives
In this exciting role as a Quality Engineer II, you will have responsibility for day-to-day manufacturing floor support in a medical device manufacturing area that supports products.
A Day in the Life
Responsibilities may include the following and other duties may be assigned.
- Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product.
- Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
- Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
- Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.
- Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
- May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and / or research and development as they apply to product or process quality.
Must Have : Minimum Requirements
Bachelor’s Degree in Engineering, Science or technical field with 2+ years of work experience in Engineering and / or Quality OR Advanced Degree in Engineering, Science or technical field with 0 years of work experience.
Nice to Have
- Audit Readiness (external and internal audit experience).
- CAPA experience (owner of CAPAs).
- Process improvements (creation and implementation of improvements).
- Experience in a manufacturing environment.
- Experience with creation and completion of change controls.
- Medical devices or Pharma experience.
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