QC Technical Coordinator

  • Location: Kennesaw
  • Type: Contract To Hire
  • Job #38816

New Opportunity- Local to Kennesaw, GA with a rapidly growing global human and animal nutrition company.
As a QC Technical Coordinator, you will be responsible for providing direct support to the continuous improvement of the laboratory initiatives of the QMS. With the guidance from the Lab Manager, you will ensure the quality of various systems throughout the department and assist with assessing and developing method and equipment validations associated with testing within the QC Labs. This is a great opportunity for a quality professional with experience within an FDA regulated facility, 2+ years of lab experience in an ISO 17025 certified facility and a Bachelors degree withing a scientific field of study.
Salary: $50k-80k/yr. depending on experience
Terms: Contract to Hire


  • Investigate, create, develop and work towards the validation of new methods, method improvements and technologies for quality control laboratory following AOAC, USP, ISO GLP or other accredited process. Conduct periodic review of Standard Operating Procedures (SOPs), Lab Methods and Forms for compliance with applicable regulations and Standards and adherence to current procedures and practices.  Submit change controls for necessary revisions.
  • Ensure all laboratory methods are validated or verified, as appropriate, and maintained in a validated state.
  • Assess, develop, and execute validations and qualifications of methods, processes, and equipment used in the labs.
  • Establish and maintain calibration protocols and maintenance records in accordance with cGMP, cGLP, ISO,and/or regulatory requirements.
  • Schedule or otherwise arrange for equipment calibration prior to calibration expiry.
  • Assist in non-conformance, CAPA’s, and process/equipment deviation investigations relating to the laboratory ensuring proper identification of failure mode, root cause, and corrective/preventive actions as well as provide clearly written summaries of findings.
  • Assist Lab Management in gathering data and trending of QC Objectives and Laboratory KPI’s.
  • Generate and present reports on departmental activities and efficiencies.


  • Minimum – 4-year university degree in science, biotechnology, or other related fields
  • Minimum – 2+ years laboratory experience in an ISO 17025 certified or equivalent laboratory or a Masters in Science, Biotechnology, or other related fields.
  • Preferred – Experience in and FDA regulated facility

**This job description is a complete list of all desired skills but not all are required.  We strongly encourage candidates who have some of the skills to apply.  We look forward to a conversation to learn more about you**

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Equal Employment Opportunity (EEO) Information

While the position you're applying for may not be for a government role, Astrix is a governmental contractor and, as such, is required to collect certain information in its applicants. Astrix is an Equal Opportunity Employer and does not discriminate against any applicant for employment, or any employee because of age, color, sex, disability, national origin, race, religion, or veteran status. Completion of these fields will not affect your opportunity for employment or the terms or conditions of your employment.

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