Full-Time

Production Operator

Posted on 12/1/2025

Curia

Curia

1,001-5,000 employees

End-to-end drug development and manufacturing

No salary listed

Albuquerque, NM, USA

In Person

Category
Biology & Biotech (2)
,
Requirements
  • High school diploma or general education degree (GED)
  • Ability to read, write and interpret documents such as safety instructions, standard operating procedures, policies, and manuals. Ability to write clearly and communicate effectively.
  • Mathematical skills to add, subtract, multiply and divide into all units of measure, using whole numbers, common fractions, decimals and percentages. Ability to draw and interpret bar graphs.
  • Reasoning ability to demonstrate understanding and effective application of written and oral instruction.
  • Computer skills in Microsoft Word, Excel, Outlook, and Access; ability to quickly adapt and learn new manufacturing software systems.
  • Must pass a background check
  • Must pass a drug screen
  • May be required to pass Occupational Health Screening
  • Must pass pre-employment assessment
  • Must be able to obtain and maintain gowning certification
  • Must be able to obtain and maintain media qualification
  • Must be able to wear a respirator
  • Physical demands include lifting up to 10 pounds regularly, up to 25 pounds occasionally, up to 50 pounds infrequently; standing, sitting, reaching; visual acuity; dexterity; occasional stooping, kneeling, twisting, crouching, crawling; ability to work in sterile/cleanroom environments with PPE; exposure to cleaning agents
  • Must be able to obtain and maintain personal protective equipment as required
  • Must pass a safety/health training as required
  • Ability to read/interpret SOPs; maintain up to date trainings
Responsibilities
  • Adhere to Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMPs), and proper aseptic techniques to ensure the production of sterile, high-quality products
  • Assemble and operate automated filling and sealing equipment aseptically
  • Accurately document and review production paperwork to ensure clarity and compliance
  • Perform in-process inspections or pre-inspections of vials as required
  • Maintain and stock gowning materials to ensure proper gowning procedures
  • Clean and sanitize work areas to maintain a sterile manufacturing environment
  • Collaborate with peers to provide mutual training and support under the guidance of Production Management
  • Read/interpret SOPs to ensure compliance
  • Maintain up to date trainings
  • Other duties may be assigned
Desired Qualifications
  • Two (2) years related experience in production, manufacturing, and/or cleanroom preferred

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

Debt Financing

Total Funding

$1.1B

Headquarters

Albany, New York

Founded

1991

Simplify Jobs

Simplify's Take

What believers are saying

  • Biologics segment expansion under Steve Lavezoli accelerates high-margin pharmaceutical outsourcing revenue growth.
  • Carterra partnership positions Curia to capture Pacific Northwest biotech demand in antibody discovery services.
  • Gerald Auer's CFO appointment signals M&A activity and potential strategic initiatives enhancing shareholder value.

What critics are saying

  • Pace Life Sciences acquisition of New Jersey lab erodes Curia's analytical testing capacity and revenue.
  • Larger CDMOs like Lonza and Catalent undercut Curia on biologics capacity, stealing biotech contracts.
  • FDA scrutiny on srRNA manufacturing defects from Replicate Bioscience Phase 1 triggers potential client exodus.

What makes Curia unique

  • Pioneer in self-replicating RNA manufacturing, demonstrated through Replicate Bioscience Phase 1 clinical trial support.
  • Integrated enzymatic doggybone DNA technology via Touchlight collaboration expands mRNA manufacturing competitive advantages.
  • End-to-end CDMO services from discovery through cGMP manufacturing differentiate Curia from specialized competitors.

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Benefits

Paid Vacation

401(k) Retirement Plan

401(k) Company Match

Tuition Reimbursement

Professional Development Budget

Growth & Insights and Company News

Headcount

6 month growth

0%

1 year growth

0%

2 year growth

0%
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