CURIA
Production Operator III
- Compensation
- Not disclosed
- Location
- Camarillo, CA, United States
- Work setup
- Not specified
- Seniority
- Not specified
- Employment
- Contract
- Experience
- Not specified
- Category
- Manufacturing
- Posted
Skills
Nice to have
- • 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. Abilit
- 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
- 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
- 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 proces
- 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 b
- 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 e
- 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 chemic
- 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 w
- 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
Full description
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