Quality Assurance Technician

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  • As an Equal Employment Opportunity Employer, DAVIS has reporting requirements which require us to invite employees to voluntarily self-identify their race/ethnicity. Submission of this information is voluntary and refusal to provided it will not subject you to any adverse treatment. The information obtained will be kept confidential.
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Quality Assurance Technician

  • Specialty:

    Manufacturing
  • Title:

    Quality Assurance Technician
    • City:

      Hoschton
    • State:

      GA
    • Zip Code:

      30548
  • Start date:

    05-29-2018
  • Status:

    Closed
  • Assignment Type:

    Contract To Hire
  • Job Id:

    45507

Description

Quality Assurance Technician:

Our Client in the Jackson County area is looking for a Quality Assurance Technician with 2+ years of experience in the pharmaceutical manufacturing industry. 

This is a first shift opportunity 8:00 am - 5:00 pm. Pay is based on experience and starts at $20 an hour. 

Responsibilities:

  • Assist in the development of lab test methods on raw materials, initial, in-process and final products, and samples collected from environmental monitoring programs at manufacturing facilities. 
  • Assist with the installation and validation of sophisticated laboratory instrumentation and computer systems to collect and record data.
  • Complete all testing, including special project / protocol testing in a timely and appropriate manner.
  • Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and cGMP regulations.
  • Participate in functions involving teams, which impact production, increase efficiency, solve problems, generate cost savings and improve quality.
  • Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors.
  • Exercises judgment within defined procedures and practices to determine appropriate action.
  • Normally receives general instructions on routine work, detailed instructions on new assignments.
  • Perform laboratory and manufacturing audits as required. Audit and update, as required, plant SOPs.
  • Perform equipment maintenance and calibrations as required.

Qualifications: 

  • Ability to multi-task and set priorities for multiple projects. Ability to deliver high quality results within set timelines.
  • Must communicate effectively (verbal and written) with supervisors and peers and be able to work cross-functionally with other groups.
  • Must be able to read and follow detailed written instructions and have good verbal/written communication skills.
  • Knowledge of chemical and biological safety procedures.
  • Strong computer skills, knowledge of Microsoft Word, Excel and PowerPoint.
  • Bachelors Degree in Chemistry, or Biological Science with Analytical Chemistry or Microbiology Laboratory coursework and/or 2+ years pharmaceutical manufacturing experience

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