Quality Control Technician

Details of the offer

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

ManpowerGroup is committed to providing equal employment opportunities in a professional, high quality work environment.
It is the policy of ManpowerGroup and all of its subsidiaries to recruit, train, promote, transfer, pay and take all employment actions without regard to an employee's race, color, national origin, ancestry, sex, sexual orientation, gender identity, genetic information, religion, age, disability, protected veteran status, or any other basis protected by applicable law.


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