Senior Production Operator III – Aseptic GMP

Curia Global, Inc.

Camarillo (CA)

Hybrid

USD 39,000 - 51,000

Full time

14 days+

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Benefits offered by this job

Generous benefit options (eligible on
Paid training, vacation and holidays (
Career advancement opportunities
Education reimbursement
401K program with matching
Learning platform
And more!

Job summary

Curia Global, Inc. is seeking a Production Operator III in Camarillo, CA to support timely manufacturing of parenteral cGMP products in an aseptic environment.

The role involves executing formulations, operating equipment, assuring GMP compliance, and assisting in SOPs and batch records. The ideal candidate has a high school diploma and at least two years in pharmaceutical manufacturing, with preferred biotech credentials.

Qualifications

  • High school diploma or equivalent.
  • Two years of experience in pharmaceutical manufacturing.

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

Skills

Reading & interpreting documents
Writing routine reports
Speaking effectively in groups
Attention to detail
Teamwork

Education

High school diploma or equivalent
Associate’s degree or biotechnology certificate (preferred)

Tools

Spreadsheet software
Word processing software
Manufacturing software

Job description

Curia Global, Inc. is seeking a Production Operator III in Camarillo, CA to support timely manufacturing of parenteral cGMP products in an aseptic environment.

The role involves executing formulations, operating equipment, assuring GMP compliance, and assisting in SOPs and batch records. The ideal candidate has a high school diploma and at least two years in pharmaceutical manufacturing, with preferred biotech credentials.

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