C

Curia

End-to-end drug development and manufacturing

Production Support Operator

Machine & Process OperationConfirmed live in the last 24 hours
Full-timeAlbuquerque, NM, USANo salary listedIn-person

About the Job

Requirements

  • A high school diploma or general education degree (GED) is required.
  • Two years of related experience in production, manufacturing, and/or cleanroom work is preferred.
  • Ability to read, write, and interpret safety instructions, standard operating procedures, policies, and manuals, and to write clearly and communicate effectively.
  • Ability to perform addition, subtraction, multiplication, and division using whole numbers, fractions, decimals, and percentages, and to draw and interpret bar graphs.
  • Ability to understand and effectively apply written and oral instructions.
  • Proficiency with Microsoft Word, Excel, Outlook, and Access, and ability to learn new manufacturing software systems.
  • Must pass a background check, drug screen, and pre-employment assessment; may be required to pass Occupational Health Screening.
  • Must obtain and maintain gowning certification and media qualification, and be able to wear a respirator.
  • Must follow safety protocols, identify and address potential hazards, and participate in safety training.
  • Must meet the position's physical demands, which can include lifting, pushing, pulling, sitting, standing, reaching, visual tasks, hand and finger dexterity, and occasional stooping, kneeling, twisting, crouching, crawling, balancing, or climbing.
  • Aseptic gowning and task-dependent personal protective equipment are required in sterile pharmaceutical manufacturing environments.

Responsibilities

  • Ensure compliance with current Good Manufacturing Practices, maintain accurate documentation, and contribute to training and process improvement to support efficient production and product quality.
  • Support timely manufacturing of parenteral products through vial preparation, fill-line operation, lyophilizer loading and unloading, and vial sealing in an aseptic environment.
  • Set up, operate, sanitize, and sterilize equipment and manufacturing areas in cleanrooms.
  • Prepare, wash, and sterilize vials; perform batch calculations and formulations; and follow applicable regulations and procedures.
  • Maintain current good documentation practices for work activities and participate in training and continuous-improvement initiatives.
  • Sanitize aseptic and controlled areas using specified solutions and equipment, following sterile-processing protocols and standard operating procedures.
  • Prepare, sterilize, clean, and decontaminate dedicated and non-dedicated manufacturing equipment in a cleanroom.
  • Compound or formulate drug solutions using raw materials and hazardous chemicals while following safety protocols and wearing appropriate personal protective equipment.
  • Follow standard operating procedures, current Good Manufacturing Practices, and aseptic techniques to produce sterile, high-quality products.
  • Assemble and aseptically operate automated filling and sealing equipment.
  • Accurately complete and review production paperwork for clarity and compliance.
  • Perform in-process or pre-inspections of vials as required.
  • Maintain and stock gowning materials for proper gowning procedures.
  • Clean and sanitize work areas to maintain a sterile manufacturing environment.
  • Collaborate with peers to provide mutual training and support under Production Management guidance.
  • Read and interpret standard operating procedures and maintain up-to-date training.
  • Perform other duties as assigned.

Desired Qualifications

  • Two years of related experience in production, manufacturing, and/or cleanroom work.

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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