C

Curia

End-to-end drug development and manufacturing

Production Operator 2

Full-Time
$25.24 - $31.97/hr
Junior
Associate's, Certification
Camarillo, CA, USA
In Person
Biology & BiotechBioprocess & Biomanufacturing

About the job

Requirements
  • High school education or equivalent.
  • One year of experience in pharmaceutical manufacturing.
  • Ability to read and interpret safety rules, operating and maintenance instructions, and procedure manuals; write routine reports and correspondence; and speak effectively before groups of customers or employees.
  • Ability to perform basic arithmetic and compute rates, ratios, and percentages, and to draw and interpret bar graphs.
  • Ability to use internet, manufacturing, spreadsheet, and word-processing software.
  • Ability to comprehend and follow standard operating procedures, current Good Manufacturing Practices, and detailed instructions to produce sterile quality products.
  • Ability to document information, events, and current Good Manufacturing Practice manufacturing processes clearly, accurately, and completely.
  • Ability to perform duties in an organized, detail-oriented manner and apply basic computer skills.
  • Must pass a background check and drug screen; may be required to pass occupational health screening.
  • May be required to obtain and maintain gowning certification and media qualification.
  • Must be able to meet the stated physical demands, including lifting up to 50 pounds and the listed vision requirements.
Responsibilities
  • Execute and support complex formulations and compounding operations according to batch records and standard operating procedures.
  • Operate and monitor formulation equipment, including mixers, tanks, filtration systems, and transfer systems.
  • Ensure adherence to Good Manufacturing Practices, safety, and data integrity requirements.
  • Support process scale-up, engineering runs, and Good Manufacturing Practice batches.
  • Assist in drafting and revising standard operating procedures, batch records, and protocols.
  • Review batch record documentation for accuracy and completeness.
  • Support technical transfer and process documentation updates.
  • Prepare and sanitize equipment for clean rooms, product compounding, and filling according to the preparation list, including disassembly and assembly.
  • Load and unload steam sterilizers and washers according to diagrams and instructions.
  • Record procedures in logbooks after completion and complete or correct batch records.
  • Sanitize aseptic and controlled production areas to reduce microbial contamination on inanimate surfaces to a safe level.
  • Perform bubble point tests on filters and read and interpret standard operating procedures to ensure compliance.
Desired Qualifications
  • An associate's degree or biotechnology certificate; a biotechnology certificate may be substituted for the equivalent combination of industry experience.
  • Previous cleanroom or current Good Manufacturing Practice experience.

About the company

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

$132M

Headquarters

Albany, New York

Founded

1991

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Simplify's Take

What believers are saying

  • Curia expanded Glasgow sterile drug product capacity in March 2026.
  • Curia completed a $4 million sterile API upgrade in Valladolid in October 2025.
  • Curia won a 2025 CDMO Leadership Award in Global Biologics.

What critics are saying

  • Curia is closing Burlington in 2026 and cutting 81 jobs.
  • Curia is working on an out-of-court restructuring with private credit lenders.
  • Asset sales like Pace’s New Jersey lab purchase signal continued portfolio shrinkage.

What makes Curia unique

  • Curia spans discovery through commercial manufacturing across small molecules and biologics.
  • Curia manufactures mRNA and self-replicating RNA, including Replicate Bioscience’s RBI-4000.
  • Curia runs 20+ global sites with sterile fill-finish and cell-line development.

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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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ALBANY, N.Y., Feb. 23, 2024 (GLOBE NEWSWIRE) - Curia, a leading contract research, development and manufacturing organization, today announced it has appointed Steve Lavezoli as vice president of biologics effective Feb. 26.

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Curia Receives 2024 CDMO Leadership Award

Curia was awarded based on the feedback of respondents in the Small Pharma category.