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Salary
≈ $40k – $72k per year (Estimated)
Location
In office (Camarillo)
Seniority
Middle · 2+ years exp

Confirmed on the employer's own hiring board on Oct 19, 2026. First seen by Alion on Sep 16, 2026. Curia scores A on the Alion truth index.

Overview
Company
Impact
Profile match
Curia is a contract research, development and manufacturing organization serving pharmaceutical and biotech companies, headquartered in Albany, New York, and known until 2021 as AMRI. With more than 30 years of history, it offers drug discovery, small molecule and API process development and manufacturing, biologics, formulation and sterile fill-finish, and has grown through acquisitions such as Euticals in Italy and Integrity Bio in Camarillo, California. It hires chemical operators and production technicians, quality control analysts, research scientists, process safety chemists, automation and utilities engineers and supply chain staff.

Production Operator III in Camarillo, CA

Build your future at Curia, where our work has the power to save lives.

Support timely manufacturing of parenteral cGMP products in an aseptic environment including executing and supporting formulation operations in a GMP-regulated environment. This role performs complex processing activities, supports troubleshooting and process improvements, and contributes to documentation development and technical writing efforts to ensure compliant and efficient manufacturing operations.

Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers’ therapies from curiosity to cure and ultimately to improve patients’ lives.

We proudly offer

  • Generous benefit options (eligible first day of employment)
  • Paid training, vacation and holidays (vacation accrual begins on first day of employment)
  • Career advancement opportunities
  • Education reimbursement
  • 401K program with matching contributions
  • Learning platform
  • And more!

Responsibilities

  • Execute and support complex formulations and compounding operations according to batch records and SOPs
  • Operate and monitor formulation equipment including mixers, tanks, filtration systems, and transfer systems
  • Ensure adherence to GMP, safety, and data integrity requirements
  • Support process scale-up, engineering runs, and GMP batches
  • Assist in drafting and revising SOPs, 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 preparation list, including disassembly/assembly
  • Load and unload steam sterilizers and washers according to diagrams and instructions
  • Record all procedures in logbooks following completion and complete/correct batch records
  • Sanitize aseptic/controlled production areas to ensure microbial contamination is reduced to safe level on inanimate surfaces
  • Bubble point test filters and read/interpret SOPs to ensure compliance
  • Other duties as assigned

Required

  • High school education or equivalent
  • Two years’ of experience in pharmaceutical manufacturing

Preferred

  • Associate’s degree or biotechnology certificate; biotechnology certificate may be substituted for the equivalent combination of experience in the industry
  • Previous cleanroom or cGMP experience

Language Skills

Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of organization.

Mathematical Skills

Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, and percent and to draw and interpret bar graphs.

Reasoning Ability

Ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form. Ability to deal with problems involving several concrete variables in standardized situations.

Computer Skills

Knowledge of Internet software; Manufacturing software; Spreadsheet software and Word Processing software,.

Other Skills and Abilities

  • Comprehend and follow SOPs, cGMPs, and detailed instructions to successfully produce sterile quality products
  • Document information, events, and cGMP manufacturing processes clearly, accurately and completely
  • Perform duties in an organized, detail-oriented manner
  • Apply basic math: measures, weights, fractions, decimals
  • Apply basic computer skills
  • Work and communicate well with others in a team environment

Other Qualifications

  • Must pass background check
  • Must pass drug screen
  • May be required to pass Occupational Health Screening
  • May be required to obtain and maintain gowning certification
  • May be required to obtain and maintain media qualification

Physical Demands

While performing the duties of this job, the employee is regularly required to talk or hear. The employee is frequently required to sit and use hands to finger, handle, or feel. The employee is occasionally required to stand; walk; reach with hands and arms; climb or balance and stoop, kneel, crouch, or crawl. The employee must regularly lift and /or move up to 10 pounds, frequently lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision and depth perception.

Work Environment

While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts; high, precarious places; fumes or airborne particles; toxic or caustic chemicals; risk of electrical shock; explosives; risk of radiation and vibration. The noise level in the work environment is usually moderate.

Pay Range: $28.61-$37.26/hour

Education, experience, location and tenure may be considered along with internal equity when job offers are extended.

We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.

All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.

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