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Curia

End-to-end drug development and manufacturing

Quality Control Analyst 2

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeHopkinton, MA, USA$80k - $85k /yrIn-person

About the Job

Requirements

  • A Bachelor's degree in Chemistry or a relevant field and 3 years of related work experience, or a Master's degree in Chemistry or a relevant field and 1 year of related work experience.
  • Must pass a background check.
  • Must pass a drug screen.
  • May be required to pass Occupational Health Screening.

Responsibilities

  • Perform analytical testing for incoming, in-process, and final products, and stability samples using equipment such as balances, pipettes, a pH meter, a UV/Visible spectrophotometer, and a Total Organic Carbon analyzer.
  • Perform chromatography (HPLC/GC, UPLC) with minimal qualification and training, wet chemistry assays, analytical chemistry assays, HPLC, GC, IR, UV, and raw material testing and/or sampling.
  • Back up analytical instrument maintenance and calibration for Quality Control.
  • Perform general laboratory equipment maintenance and laboratory housekeeping, and prepare the laboratory for audits.
  • Perform or assist with Quality Control method qualifications, transfers, and validations.
  • Perform Quality Control method development.
  • Perform cleaning validation studies.
  • Assist with evaluation of new equipment and processes.
  • Assist in reviewing Quality Control data and provide summaries to management as needed.
  • Assist Quality Control Management, as needed, in completing out-of-specification (OOS), deviation, and corrective and preventive action (CAPA) investigations for Quality Control.
  • Back up Quality Control analytical sample receipt for internal and outside laboratory testing, including login, processing, shipment, tracking, distribution of test results, and closure.

Desired Qualifications

  • Experience with chromatography, including SEC-HPLC, UPLC, and related methods for purity and impurity analysis.
  • Experience with electrophoretic techniques, including CE-SDS and cIEF (e.g., Maurice/PA800 platforms), for protein characterization and charge/size variants.
  • Experience with ligand-binding assays, including ELISA (e.g., potency, HCP, residual Protein A) and/or Octet/BLI, for binding and functional characterization.
  • Experience with molecular methods, including qPCR-based assays (e.g., residual DNA, mycoplasma).
  • Experience with biochemical assays, including UV/Vis, mBCA, pH, conductivity, osmolality, and general wet chemistry techniques.
  • Experience with product quality assessments, including visual appearance, subvisible particles, and integrity testing.

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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