C

Curia

End-to-end drug development and manufacturing

Aseptic Core Monitor 1

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

About the Job

Requirements

  • An associate’s degree in Microbiology or a related field of study and at least three years of previous professional experience, or a bachelor’s degree in Microbiology or a related field of study and at least two years of previous professional experience; the bachelor’s-degree pathway is preferred.
  • Industrial Good Manufacturing Practice experience in an FDA-regulated pharmaceutical environment.
  • Aseptic processing experience, including proficiency in aseptic gowning qualifications.
  • Ability to read and interpret safety instructions, standard operating procedures, technical procedures, and governmental regulations.
  • Ability to execute arithmetic operations across units of measurement using whole numbers, fractions, decimals, and percentages, and a strong grasp of algebraic and geometric principles.
  • Ability to define problems, collect data, establish facts, draw valid conclusions, interpret technical instructions in mathematical or diagram form, and deal with abstract and concrete variables.
  • Capability in manufacturing and internet software and proficiency with Microsoft PowerPoint, Excel, Word, and Outlook.
  • Ability to obtain and maintain gowning certification and media qualification.
  • Must pass a background check and drug screen; may be required to pass Occupational Health Screening and wear a respirator.

Responsibilities

  • Perform daily visual audits.
  • Communicate effectively with production partners and escalate urgent matters to facilitate path-forward decisions.
  • Make decisions and assess risks in support of aseptic processes and tier-one decision-making activities.
  • Deliver coaching and training, and break down complex concepts to teach others.
  • Record and track data.
  • Review documentation and read and interpret standard operating procedures to ensure compliance.
  • Collaborate within and between departments with management, manufacturing and support technicians, and senior MQA On the Floor team members.
  • Maintain up-to-date training.
  • Identify and address potential hazards, follow established safety protocols, participate in safety training, and promote a safe and healthy work environment.

Desired Qualifications

  • A bachelor’s degree in Microbiology or a related field of study and at least two years of previous professional experience.
  • Basic quality-tool experience, such as Pareto charts, histograms, cause-and-effect analysis, and root cause analysis.

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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