Production Operator

The O'Connor Group

Posted on : 17-04-2025

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1 Vacancy

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Job Location

Thousand Oaks, CA - USA

Monthly Salary

Not Disclosed

Salary Not Disclosed

Vacancy

1 Vacancy

Posted on : 17-04-2025

Job Description

Company Summary:

20bloc Inc. is a nonclinical stage biopharma company creating breakthrough proteinbased to save lives. We are developing a safe and effective hemoglobinbased oxygen carrier for first response organ preservation and oxygen therapy. We value and encourage innovations through robust information exchange hard work and team

interaction. We are collaborative. We are intellectual. We are handson.

Position Overview: Operate equipment and perform established production process including troubleshooting problem solving and process improvements and ensuring production consistency continuity and product quality in our current facility and future GMP facility. This is a fulltime onsite position in Thousand Oaks CA.

Key responsibilities:

Operate monitor and troubleshoot biopharma process and equipment (e.g. bioreactors centrifuges chromatography systems filtration skids) and ensure consistency continuity quality and production schedule.

Produce and maintain accurate and timely batch records equipment logs and other required GMP documentation and ensure verifiability and traceability.

Perform routine equipment cleaning sterilization and calibration according to SOPs and maintenance schedules and ensure robustness.

Conduct environmental monitoring inprocess sampling and basic laboratory testing as required.

Assist in audits inspections and training sessions as required.

Collaborate with QA QC Process Development Engineering and Management to support tech transfer compliance program and GMP requirements and production timelines.

Requirements

Requirements:

High school diploma GED or higher qualifications.

1 3 years of GMP experience in a biotech pharmaceutical or similar regulated manufacturing environment.

Experience with bioreactors filtration and chromatography skids and fluid handling.

Excellent attention to detail documentation accuracy and clarity and communication skills.

Familiarity with cGMP documentation practices batch records and electronic systems (e.g. MES LIMS) a plus.

Physically capable of lifting up to 25 lbs and standing for extended periods.

Benefits

Medical dental and vision plans

120 hours paid time off (PTO)

12 paid holidays annually

401(k) U.S. retirement savings plan

Employee assistance program

High school diploma, GED or higher qualifications. 1 3 years of GMP experience in a biotech, pharmaceutical, or similar regulated manufacturing environment. Experience with bioreactors, filtration and chromatography skids, and fluid handling. Excellent attention to detail, documentation accuracy and clarity, and communication skills. Familiarity with cGMP documentation practices, batch records, and electronic systems (e.g., MES, LIMS) a plus. Physically capable of lifting up to 25 lbs and standing for extended periods.

Employment Type

Full Time

Company Industry

Key Skills

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About Company

The O'Connor Group

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Production Operator

The O'Connor Group

Job Description

Requirements

Benefits

Employment Type

Company Industry

Key Skills

About Company

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