Job Title: Quality Control Technician
Location: Saint Paul, MN 55117 (100% onsite role)
Client: Abbott
Max Payrate: $26/hour on W2.
Duration: 12 months with possibility of extension or conversion.
Overview:
As Quality Assurance Technician, you will support manufacturing in the Structure Heart Division of Abbott, reporting to the Manager of Quality.
• Support document control, such as taking ownership of change order/change activity for coworker
• Maintain Device History Record (DHR)/Lot History Record (LHR) log - creation of new lot numbers upon request and subsequent updates as appropriate
• Assist in and/or perform final review of manufacturing DHR/LHR at close of or during manufacturing process and product release
• Compile and archive completed and approved DHR/LHR
• Compile and archive completed and approved incoming inspection records
• Support incoming inspection as needed - understand and utilize the capability of measuring tools/fixtures; understand material specifications/inspection requirement of the components and parts; properly document inspection outcome
• Support equipment controls and calibration/PM activities such as coordination with calibration/PM subject matter expert, handling the physical logistics and update of equipment log
• Compile and archive various quality records in accordance with internal procedures and external standards/regulations
• Communicate with coworkers and management if a nonconformance incident occurs
• Support cross-functional areas as needed.
EDUCATION AND EXPERIENCE
• High school diploma or equivalent qualification.
• 1+ years' experience working in manufacturing, or related field.
• Excellent knowledge of MS Office and Excel.
• Good math and technical skills.
• Working knowledge of quality control standards, and when necessary, testing techniques as well.
• Positive and cooperative communication, both verbal and written, and effective collaboration with all levels of employees, customers, contractors, and vendors.
• Working knowledge of Quality Systems, FDA regulations, ISO 13485 and applicable worldwide regulator requirements.
• Multitasks, prioritizes and meets deadlines in a timely manner.
• Strong organizational and follow-up skills, as well as high level of attention to detail and accuracy.
• Ability to maintain regular and predictable attendance.
• Must be an effective team player with the ability to train other technicians.
Preferred
• 1+ years prior medical device experience preferred