Microbiologist Job at Kelly Science, Engineering, Technology & Telecom, Vista, CA

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  • Kelly Science, Engineering, Technology & Telecom
  • Vista, CA

Job Description

Microbiologist

Our client is seeking a Microbiologist for a direct-hire position at a cutting-edge facility in Vista, CA. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.

Pay: $33/hour

Schedule: Day shift. Onsite

Overview

Our client is an industry-leading company at the forefront of scientific innovation, dedicated to quality control and product safety. As part of our Laboratory team, you will play a pivotal role in ensuring the integrity of raw materials, in-process goods, finished products, and environmental samples.

What you will be doing:

  • Performing microbiological testing on raw materials, in-process products, finished goods, and environmental samples using compendial methods (USP, AOAC, FDA-BAM) as well as validated in-house protocols
  • Executing testing for microorganisms such as E. coli, Salmonella, Staphylococcus, Yeast, and Mold
  • Reviewing and understanding Standard Operating Procedures (SOPs) and utilizing documentation tools to maintain QC data, reports, and corrective action summaries
  • Collaborating effectively with team members and management, communicating progress and status as needed
  • Ensuring compliance with GLP (preferred), with consideration given to GMP experience
  • Supporting water quality and environmental monitoring programs, including bioburden testing, TOC, and conductivity
  • Working in a climate-controlled lab and production environments with appropriate safety equipment

Qualifications:

  • Bachelor’s degree in microbiology (strongly preferred), chemistry, biology, biochemistry, or related field
  • Solid background in laboratory testing, including aseptic technique, serial dilutions, and microorganism enumeration
  • 3-5 years’ experience in a microbiological laboratory, preferably in a regulated GLP/GMP setting, or an MSc with at least 1 year’s related experience
  • Experience with compendial methods (USP, AOAC, FDA-BAM) and in-house validation
  • Demonstrable proficiency in SOPs, documentation tools, and QC reporting
  • Effective oral and written communication skills, ability to multi-task, and work in a fast-paced environment
  • Good computer skills in Microsoft Word, Access, Excel, and preferred LIMS experience

What happens next:

Once you apply, you’ll proceed to next steps if your skills and experience are a good fit. Even if this position isn’t the perfect match, you’re still in our network and our expert Science & Clinical recruiters will connect you with additional opportunities.

Job Tags

Day shift,

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