C

Curia

End-to-end drug development and manufacturing

Environmental Monitoring Analyst 1

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

About the Job

Requirements

  • A high school diploma or general education degree (GED) is required.
  • Two years of experience in an Analyst position is preferred.
  • Two years of related experience in production, manufacturing, and/or a cleanroom is preferred.
  • Skilled in Microsoft Word, Excel, and Outlook, with the ability to quickly adapt to new manufacturing software systems.
  • Must pass a background check and drug screen; may be required to pass Occupational Health Screening.
  • Must be able to obtain and maintain gowning certification and media qualification, and be able to wear a respirator.
  • Must be able to meet the position’s physical demands, including lifting, pushing, and pulling up to 50 pounds, and performing applicable standing, reaching, and other physical activities.
  • Must comply with applicable personal protective equipment and safety requirements in office, manufacturing, or warehouse environments, including aseptic gowning in sterile pharmaceutical manufacturing areas.

Responsibilities

  • Perform viable and non-viable environmental monitoring of cleanrooms under USP and EU specifications.
  • Prepare paperwork, supplies, and equipment daily for environmental monitoring testing in a cleanroom setting.
  • Perform microbial plating of personnel during manufacturing and personnel qualification.
  • Collect data from the particulate monitoring and audit systems to ensure appropriate sensors are activated.
  • Resolve environmental equipment malfunctions or errors.
  • Perform non-routine or infrequent sampling, such as semi-annual static particulate monitoring and quarterly compressed air monitoring.
  • Complete current Good Manufacturing Practice (cGMP) documentation and review sampling worksheets for documentation errors.
  • Maintain current training status on equipment, procedures, and test methods, and keep trainings up to date.
  • Read and interpret Standard Operating Procedures (SOPs) to ensure compliance.
  • Promote a safe and healthy work environment by identifying and addressing potential hazards, following safety protocols, participating in safety training, and fostering team awareness and responsibility.
  • Perform other duties as assigned.

Desired Qualifications

  • Foster a collaborative and positive work environment.
  • Champion change.
  • Demonstrate strong attention to detail.
  • Demonstrate strong writing skills.

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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