bioMérieux is hiring a

Template Control Laboratory Technologist I

Salt Lake City, United States
Full-Time
Job Summary:
 
The Template Control Laboratory Technologist (LT) works with a team that formulates DNA and RNA template control components to support the company’s in vitro diagnostic products’ research and development, manufacturing, validations, and quality control efforts. The LT-I will use established methods and techniques to maintain the lab’s DNA and RNA template inventory, perform template manipulations and verification including diluting, aliquoting, mixing, quantitative PCR, quantitative RT-PCR, and FilmArray analysis, perform template and control mix formulations, and dispense template and control mixes to dependent departments in accordance with the company’s quality system.
 
The LT-I will receive general instruction on routine work, perform lab duties under supervision, and receive training and additional instruction for new tasks as needed.
 
Essential Job Duties and Responsibilities:
  • Perform all work in compliance with company policy and within the guidelines of BioMerieux’s Quality System.
  • Ensure production events are completed per the production schedule. 
  •  Perform general lab maintenance duties, conduct studies, collect data, and keep an accurate record of all work.
  • Assist with maintaining inventory of DNA and RNA template, pouch control mixes, and omega QC mixes.
  • Utilize sterile technique to perform manipulations and verifications of DNA and RNA templates including diluting, aliquoting, formulating, qPCR, qRT-PCR, and FilmArray analysis.
  • Utilize sterile technique in working with microorganisms, including liquid and plate cultures, quantification, dilution, and storage.
  • Maintain organization and cleanliness of assigned production area(s).
  • Distribute controls and omega mixes to dependent departments.
  • Participate in continuous improvement efforts as assigned.
  • Maintain records in compliance with regulatory requirements, Good Manufacturing Practices, Standard Operating Procedures, and as required by the Quality System.
  • Performs other duties as assigned.
 
Training and Education:
  • B.S. in chemistry, biology, or a related field, or hold an Associate’s degree and have exceptional lab experience.
 
Experience:
  • Minimum 6 months previous experience in a laboratory setting (either academic or professional) is required.
  • Previous cGMP experience is strongly preferred.
 
Knowledge, Skills, and Abilities:
  • Knowledge of proper pipetting technique
  • Mathematic competency
  • Excellent attention to details
  • Ability to accurately follow both written and verbal instruction
  • Demonstrated proficiency with Microsoft Office Suite
  • Effective communication skills, both written and verbal
  • Highly collaborative and team oriented
 
Physical Requirements:
  • Must be able to perform duties wearing a Powered Air Purifying Respirator (PAPR).
  • Must be able to safely lift 25lbs.

 

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