C

Curia

End-to-end drug development and manufacturing

Lyophilization Technician 1

Machine & Process OperationConfirmed 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.
  • Experience working in a current good manufacturing practice (cGMP)-regulated environment is required.
  • A basic understanding of lyophilization processes or similar automated manufacturing systems is required.
  • The candidate must be able to follow detailed procedures and maintain accurate documentation.
  • The candidate must be able to work independently and manage responsibilities during off-shift operations.
  • The candidate must be able to read and interpret safety instructions, standard operating procedures, policies, batch records, and manuals, and write clearly and communicate effectively.
  • The candidate must be able to perform basic arithmetic using whole numbers, common fractions, decimals, and percentages, and draw and interpret bar graphs.
  • The candidate must be able to demonstrate understanding and effective application of written and oral instructions.
  • The candidate must be proficient in manufacturing software and Microsoft Office applications, including Word, Excel, Outlook, and PowerPoint.
  • The candidate must be able to work at elevated heights.
  • The candidate must be able to pass a background check and drug screen, and may be required to pass occupational health screening.
  • The candidate must be able to obtain and maintain gowning certification and wear a respirator.
  • The candidate must be able to perform frequent bending, reaching, stooping, kneeling, climbing, and standing for extended periods.
  • The candidate must be able to lift, maneuver, and install lyophilizer spacer bars and associated equipment components; lift and carry materials and equipment up to 50 pounds; and perform physical inspections of lyophilizers and associated manufacturing equipment.
  • The candidate must be able to climb vertical ladders and work safely at elevated heights, in confined manufacturing and cleanroom environments, and around steam, pressure systems, vacuum systems, and industrial manufacturing equipment.
  • The candidate must be able to work around piping temperatures up to 127°C and as low as -80°C.
  • The candidate must be able to wear required personal protective equipment, including full cleanroom gowning and respiratory protection, for extended periods.
  • The candidate must be able to perform repetitive motions associated with manufacturing operations and equipment setup, and work extended shifts in cleanroom and control room environments.
  • The candidate must have visual acuity sufficient to monitor equipment status, alarms, batch records, gauges, and process data, and be physically capable of responding to manufacturing issues and operational needs throughout the facility.

Responsibilities

  • Execute lyophilization operations using SERAIL and IMA equipment in accordance with batch records, standard operating procedures, and current good manufacturing practice requirements.
  • Ensure lyophilizers are cleaned, sterilized, and tested for leaks before manufacturing.
  • Operate lyophilizers according to product specifications, including temperature, pressure, time, and validated cycle parameters.
  • Monitor lyophilization cycles and review process data to ensure adherence to validated cycles and product standard operating procedure requirements.
  • Spend extended periods in the control room overseeing lyophilization cycles, data trends, and system alarms.
  • Perform routine in-process checks and ensure accurate, contemporaneous documentation in paper-based and electronic systems.
  • Support loading and unloading of lyophilizers within classified cleanroom environments, including Grade A (ISO 5) areas.
  • Identify process deviations, perform initial troubleshooting, and escalate issues through established 24/7 management channels.
  • Communicate with production and engineering staff regarding the status of lyophilization operations and assist other shifts as needed.
  • Assist with equipment setup, cleaning, and basic maintenance activities.
  • Follow standard operating procedures, current good manufacturing practices, safety practices, and good aseptic techniques to produce sterile quality products.
  • Perform aseptic gowning for various classifications of cleanroom areas.
  • Document and review associated paperwork for accuracy and clarity.
  • Work with peers to support training activities as directed by management.
  • Maintain up-to-date training requirements and comply with safety, quality, and regulatory standards.
  • Perform other duties as assigned.
  • Work the overnight shift from 6:00 PM to 6:30 AM; move between shifts based on staffing needs, including vacation and sick time coverage, and work different shifts or extended hours during maintenance shutdown periods.

Desired Qualifications

  • Two years of related experience in production, manufacturing, and/or cleanroom work is preferred.
  • A technical or associate degree is preferred.
  • Hands-on experience with SERAIL and/or IMA lyophilizers is preferred.
  • Experience in aseptic or sterile manufacturing environments, including Grade A (ISO 5) cleanrooms, is preferred.
  • Familiarity with automated control systems such as SCADA is preferred.
  • EPA certification is preferred but not required.

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

Recently Posted Jobs

Explore more opportunities at Curia

See more jobs