Engineer II

Job Title: Engineer - II Duration: 06 Months Location: Draper, UT 84020 Summary: The main function of a Quality engineer II is to support movement of production lines from one building to another. The Quality Engineer will support tasks assigned by the project engineer lead for the production line movement activities. The Quality engineer will help create, execute, and review validations and qualifications associated with the production lines being moved. Job Responsibilities: • Support validation and qualification activities associated with moving production manufacturing lines between buildings. • Create, execute and review protocols and reports associated with requalification and validation activities. • Support process confirmation activities for manufacturing line moves. • Support calibration and confirmation activities associated with inspection and testing equipment • Support physical movement of portable equipment between buildings as necessary. Skills: • Creativity, verbal and written communication skills, analytical and problem-solving ability. • Team player and detail oriented. • Experience as a quality engineer working in medical device industry. • Ability to create and execute protocols and reports related to qualification and validation activities. • Background in validation of manufacturing lines, inspections, test methods, etc. What Makes Someone Successful Here: 1. Able to Integrate Quickly • Builds relationships across an existing team fast • Knows how to navigate who to go to for what • Comfortable stepping into an established environment without friction 2. Operates Independently • Can take a task (like writing a validation protocol) and run with it • Doesn't wait for step-by-step instruction • Checks alignment when needed, but doesn't stall progress 3. Comfortable in Ambiguity • Project details may evolve • Needs to stay productive without everything being perfectly defined Required Experience & Background: • Bachelor's degree in engineering (required) • 2 to 4 years of experience as a Quality Engineer • Experience in medical device or regulated manufacturing environment strongly preferred • Hands-on experience with: o Validation and qualification activities o Manufacturing line processes o Inspection and testing methods Core Skills • Strong written and verbal communication • Analytical thinking and problem-solving • Detail-oriented with strong documentation discipline • Team-oriented but capable of independent execution Education/Experience • Bachelor's degree in engineering required. • 2-4 years experience as a Quality Engineer required • Experience in medical device or regulated manufacturing environment strongly preferred Hands-on experience with o Validation and qualification activities o Manufacturing line processes o Inspection and testing methods