What are the responsibilities and job description for the Quality Engineer position at Trillium Professional?
Trillium Professional is now seeking a Quality Engineer in Holdrege, NE! This is a long term project that could be converted to a full time opportunity.
The Quality Engineer is responsible for supporting sustaining activities through the application of Quality Engineering skills for medical devices. This person will understand, improve, and control operational processes to realize predictable product flow while satisfying established embecta standards of quality. Additional responsibilities include cross functional support for the Quality Engineering and Quality Systems group. This position is responsible to build sound technical and organizational competence within area of responsibility. Ensure the systems comply with applicable government regulations and standards. Comply with all embecta quality policies, procedures, and practices through consistent application of sound quality engineering/assurance principles.
Essential functions include but are not limited to:
-Support the plant on assigned product initiatives with technical expertise and determine associated resource needs to accomplish project goals.
-Provide critical quality engineering direction to Branding project with respect to generally accepted quality engineering tools/principles, such as root cause analysis, FMEAs, risk mitigation, validation, DOE/other process improvement tools, measurement and measurement systems analysis, sampling, and control plans.
-Applies moderate level application of technical principles, theories, concepts, techniques, and quality sciences / tools.
-Develops solutions to routine problems of moderate scope.
-Maintain alignment to company quality policies, procedures, and practices through consistent application of sound quality assurance principles. Make basic procedural updates.
-Demonstrates working knowledge of applicable regulatory, Corporate and/or Unit requirements.
-Is an extended team member representing Site Quality on new product development projects and a team member for sustaining engineering projects.
-Establishes a strong working relationship with all levels of operations to appropriately monitor and analyze in-process inspection, process control activity, waste and reject rates, PM compliance, environmental control, and customer complaint levels in order to take a lead role in identifying and documenting continuous improvement projects.
-Approve protocols and reports for all validation and change control activities to ensure compliance to established procedures.
-Utilize Lean and Six Sigma problem solving methods, data analysis tools and techniques to support department validation efforts around continuous improvement.
Pay rate is $42 per hour. Apply now!
Requirements:
-B.S. degree Required.
-B.S. degree in Engineering (Industrial, Mechanic) Desired
-3 Years Quality experience including Validation and Quality Engineering responsibilities.
-Demonstrate success with statistical and problem-solving methodologies.
-Excellent knowledge of the principles for Quality Engineering and Quality management as related to validation process on medical devices.
-Strong understanding of failure analysis, test methods and engineering tolerances.
-Strong verbal, written and interpersonal skills.
-Proficient with Minitab or other statistical software, MS Word, Excel, and MS project.
Six Sigma Certification Desired:
-ASQ CQE
-Working knowledge of 21CFR820, ISO 13485.
Salary : $42
