Tech 1, Quality Assurance

Job Title - Quality Assurance Technicain/Inspector - Req Exp in Incoming Inspection

Number of Positions - 1

Job Location - 1022 Corporate Park Way, Mebane, North Carolina, United States of America, 27302

Duration: 3 Months

Job Description

• Pay Rate: $20 - $21.50/hr (Pay rate will be detemined at time of offer )
  1st Shift; Mon-Thurs; 7am-530pm
• QA 1 will be mostly incoming inspection.
• Independently perform incoming inspection of a wide variety of materials, analyze inspection results versus specifications, ensure correct sampling plans are used
• Detect nonconforming conditions during inspection and accurately document each condition.
  
  This position is primarily responsible for execution of incoming inspection. Inspections include visual, dimensional, and functional inspections on a wide variety of products. This position monitors compliance with GMP and GDP, and reports infractions appropriately. Additional responsibilities include analysis of results, product sampling, label verification, determining product disposition, detecting nonconforming conditions, investigating root causes of nonconforming conditions, and accurately recording and reporting quality data. This role is responsible for working within an established framework of compliance and implementing improvements to product quality and the quality system.
  Independently perform incoming inspection of a wide variety of materials, analyze inspection results versus specifications, ensure correct sampling plans are used.
  Independently perform inspection of labels used in the production of products to ensure alignment with specifications.
  Detect nonconforming conditions during inspection and accurately document each condition. Demonstrate a bias for action to determine scope of nonconforming conditions, and segregate nonconforming products to prevent further use.
  Perform basic lab support functions, including preparation of basic standards and reagents, Obtaining samples from production, PM, 5S, and cleaning and handling of hazardous waste as appropriate.
  Responsible for maintenance of retention samples, and electronic and physical storage of device history records.
  Must perform work in a safe manner adhering to gowning and PPE procedures.
  Participation in continuous improvement activities is required (e.g. kaizen).
  Additional responsibilities as assigned by management.
  
  Education and Experience:
  High School Diploma/GED with a minimum of 2 years related QC or manufacturing experience.
  Basic knowledge of SAP is preferred.
  Experience working in an FDA regulated environment is highly desirable.
  
  Knowledge and Skills:
  General Proficiency in Microsoft Office
  Demonstrated understanding of sampling techniques and inspection standards.
  Basic math skills and the ability to utilize Excel for basic calculations and graphing.
  Must be able to speak, read, and write English fluently as well as write technically and summarize information into data reports using Microsoft Word.
  Excellent attention to detail with a high degree of accuracy and the ability to work independently and in team situations.
  Excellent observation skills with a bias for "corrective action" and improve work environment processes and procedures.
  Demonstrated ability to make critical decisions regarding product quality or quality system compliance.
  Ability to assess and articulate risk when evaluating a situation.
  Knowledge of basic validation, equipment calibration, and changing requirements.
  Demonstrated understanding of the use of calibrated equipment.
  Proven capability to prioritize responsibilities and complete tasks on schedule.
  Must be able to work independently in a fast-paced manufacturing environment.
  
  Physical Demands: Ability to stand for long periods of time. Ability to lift 25 lbs. Ability to do repetitive motion.