Quality Control Microbiologist

Quality Control Microbiologist


Job ID: 10173696

Vacaville, CA, US

Scientific

Bachelors Degree

Full Time, Temp to Hire

$28 per hour

Entry Level

On-site

Biotechnology/Pharmaceuticals

First Shift (Day)

Vacaville, CA, US

$28 per hour

Entry Level

Full Time, Temp to Hire

Biotechnology/Pharmaceuticals

On-site

Scientific

Bachelors Degree

First Shift (Day)

Job details

Kelly® Science & Clinical is seeking a Quality Control Analyst for a contract-to-hire opportunity with one of our clients, a biopharmaceutical company focused on metabolic diseases in Vacaville, CA. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poised to advance your career, join us as we pioneer progress in the biotechnology and medical device industries.
Workplace: Vacaville, CA.
Position Title: Quality Control Analyst, Microbiology
Position Type: 6-month Contract
Pay rate: $28 hour
Quality Control Analyst I, Microbiology
Summary:
Join our client’s Quality team as a Microbiology QC Analyst, where you will play a vital role in environmental monitoring and analytical testing to ensure compliance with cGMP standards. You’ll perform essential lab assays and support sample testing to maintain product and process integrity. This is an excellent opportunity to launch your career in a collaborative, fast-paced lab environment while developing hands-on expertise in advanced analytical methods.

Key Responsibilities:

  • Perform routine environmental monitoring (EM) in GMP cleanrooms, including air and surface sampling.

  • Collect and test water and steam samples for bioburden, endotoxin, and conductivity per USP requirements.

  • Conduct growth promotion tests on culture media.

  • Analyze test results, document findings, and support investigations into non-conformances (OOS, OOE, OOT).

  • Keep lab space organized, fully stocked, and inspection-ready.

  • Build proficiency in new analytical methods and support general lab operations.

Skills & Attributes:

  • Experience in cGMP quality control or stability labs preferred.

  • Ability to follow procedures with high accuracy and minimal supervision.

  • Strong attention to detail, documentation excellence, and communication skills.

  • Computer proficiency (Word, Excel, Windows); comfort learning lab instruments and software.

  • Ability to work independently and collaboratively with teammates.

  • Previous experience with environmental monitoring, TOC, endotoxin, bioburden, or conductivity testing is a plus.

  • Capable of lifting up to 25 lbs and meeting routine vision requirements.

Qualifications:

  • Bachelor’s degree in Biology, Microbiology, Biochemistry, Chemistry, or a related field.

  • 0–3 years’ relevant laboratory experience preferred

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