Aseptic GMP Operator II – Pharma Manufacturing

Curia Aalborg ApS; Camarillo (CA); On-site; USD 52,000 - 66,000; Full time

Benefits offered by this job

Generous benefit options

Paid training

Vacation and holidays

Career advancement

Education reimbursement

401K with matching

Job summary

Curia is hiring a Production Operator II in Camarillo, CA to support aseptic manufacturing of parenteral products. You will perform complex formulations, operate mixers and transfer systems, and ensure GMP compliance while assisting in documentation and SOP updates.

Ideal candidates have a high school diploma and at least 1 year in pharma manufacturing, with preferred biotech training or an associate degree. Strong teamwork and meticulous record-keeping are essential.

Qualifications

• High school education or equivalent.
• At least 1 year of experience in pharmaceutical manufacturing.
• Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.
• Familiarity with GMP/cGMP and sterile manufacturing environment.
• Ability to pass background check and drug screen.

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.
• Draft and revise SOPs, batch records, and protocols.
• Review batch record documentation for accuracy and completeness.

Skills

Teamwork

Documentation

Attention to detail

Basic math

Computer literacy

Education

High school diploma or equivalent

Associate’s degree or biotechnology certificate

Tools

Internet software

Manufacturing software

Spreadsheet software

Word processing software

Job description

Curia is hiring a Production Operator II in Camarillo, CA to support aseptic manufacturing of parenteral products. You will perform complex formulations, operate mixers and transfer systems, and ensure GMP compliance while assisting in documentation and SOP updates.

Ideal candidates have a high school diploma and at least 1 year in pharma manufacturing, with preferred biotech training or an associate degree. Strong teamwork and meticulous record-keeping are essential.