C

Curia

End-to-end drug development and manufacturing

Microbiologist 2

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeAlbuquerque, NM, USANo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree in a scientific discipline is required; microbiology is preferred.
  • Three years of previous professional experience are required.
  • Strong organizational skills and the ability to prioritize and multitask in a fast-paced environment are required.
  • A minimum of three years of industry experience in a GMP or GLP environment is preferred.
  • Proficiency in validating and qualifying laboratory microbiological techniques is preferred.
  • Proficiency with computers and spreadsheets is required.
  • Previous experience in pharmaceutical cleanroom environments is required.
  • Knowledge of FDA cGMPs (21 CFR 211) is required.
  • The ability to pass a background check and drug screen is required.
  • The employee must be able to perform the stated physical demands, including lifting up to 50 pounds occasionally, and work around the listed laboratory and workplace hazards.

Responsibilities

  • Perform endotoxin and bioburden testing for water, and endotoxin, sterility, and bioburden testing for raw materials, in-process materials, intermediates, and final products.
  • Perform cleanroom environmental monitoring in accordance with USP and EU specifications.
  • Read, trend, and report environmental, personnel, in-process, raw material, finished product, and water testing results.
  • Perform microbial characterization using Gram stain, catalase, oxidase, and coagulase tests, and prepare and send samples for microbiological identification.
  • Maintain historical files on organisms found in classified areas, including microbial identification and trending.
  • Perform line-clear and line-start verifications and inspect media fills.
  • Perform sterility assays, including biological indicator testing, growth-promotion testing of incoming microbiology laboratory media, and microbial limits and enumeration testing.
  • Receive, log in, process, track, and distribute results for QC microbiological samples, and close out sample records.
  • Initiate out-of-specification or environmental-monitoring excursion investigations and support general QC microbiology laboratory activities.
  • Read and change charts; clean and maintain equipment; maintain supplies and inventory; and perform general laboratory housekeeping.
  • Facilitate the revision and release of controlled documents and mandatory SOP reviews and month-end reports.
  • Provide oversight for projects to update and maintain official document templates.
  • Direct and manage the Change Control System.

Desired Qualifications

  • ISO 9001, ISO 13485, and ISO 17025 knowledge is a plus.

About the Company

Curia

End-to-end drug development and manufacturing

Curia is a contract development and manufacturing organization (CDMO) that partners with pharmaceutical and biotech companies to move medical breakthroughs from concept to market. It provides end-to-end services across the drug development lifecycle, including early research, method development and validation, preformulation, material science, solid-state chemistry, and package device testing. Revenue comes from service contracts for specialized capabilities and expertise, with clients ranging from small startups to large pharma. Curia also collaborates with industry leaders to advance continuous flow development and manufacturing programs. The company differentiates itself through flexible and scalable solutions, deep scientific expertise, and state-of-the-art technology that help clients accelerate development timelines while navigating discovery to commercialization. Its goal is to enable efficient, reliable progression of drug candidates from conception through to market approval.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Albany, NY
Founded
1991

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