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Curia

End-to-end drug development and manufacturing

Quality Control Microbiologist 2

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeHopkinton, MA, USA$74k - $85k /yrIn-person

About the Job

Requirements

  • A Bachelor's degree in a relevant field and at least 3 years of industry experience in a GMP, GLP, or pharmaceutical cleanroom environment, or a Master's degree in a relevant field and 1 year of related work experience.
  • Must pass a background check and drug screen; may be required to pass Occupational Health Screening.

Responsibilities

  • Initiate out-of-specification/other testing investigations or environmental monitoring excursion investigations.
  • Initiate quality events, including deviations, invalid assay investigations, corrective and preventive actions, and change controls.
  • Perform microbiological testing for endotoxin, bioburden, and total organic carbon in water.
  • Perform microbiological testing for endotoxin, sterility, and bioburden in raw materials, in-process materials, intermediates, and final products.
  • Perform environmental monitoring of clean rooms under ISO and EU specifications.
  • Read, trend, and report environmental, personnel, in-process, raw material, finished product, and water bioburden testing results.
  • 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.
  • Perform bacteriostasis and fungistasis assays, growth-promotion testing of incoming microbiology laboratory media, and other tests as trained and assigned.
  • Receive QC microbiological samples for internal testing; log, process, track, distribute test results, and close out samples.
  • Assist QC management with authoring, reviewing, and approving documentation.
  • Assist QC management with suite and purified water system requalification.
  • Perform compendial testing such as pH, conductivity, and osmolality.
  • Support raw material handling and testing.
  • Support general QC microbiology laboratory activities, including chart reading and changing, equipment cleaning and maintenance, supply and inventory maintenance, and laboratory housekeeping.

Desired Qualifications

  • Proficiency in validation and qualification of laboratory microbiological techniques.
  • Knowledge of FDA current Good Manufacturing Practices (21 CFR 211) and ISO 9001, ISO 13485, and ISO 17025.

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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