Manufacturing Associate - Thousand Oaks CA

The Fountain Group is currently seeking a -------
- Manufacturing Associate I for a prominent client of ours. This position is located in --Newbury Park (Thousand Oaks), CA. Details for the position are as follows:

Title: Manufacturing Associate I

Location: Newbury Park (Thousand Oaks), CA

Pay: $29.24–$28.26/hr

Duration: 7 Months

• Execute manufacturing operations in a cGMP-regulated biopharmaceutical environment.

• Set up, operate, sanitize, and tear down manufacturing equipment including process tanks, filtration systems, autoclaves, portable mixers, and CIP/SIP systems.

• Prepare media and buffer solutions for manufacturing processes.

• Perform aseptic sampling and manufacturing activities in cleanroom environments.

• Monitor and document critical process parameters in accordance with GMP/GDP requirements.

• Perform equipment cleaning, routine maintenance, and room sanitization activities.

• Generate and manage manufacturing documentation, work orders, and minor document change controls.

• Support process validation, equipment validation, and manufacturing data analysis.

• Investigate and troubleshoot atypical process conditions.

• Support continuous improvement initiatives within manufacturing operations.

• cGMP and GDP compliance within pharmaceutical or biotechnology manufacturing.

• Operation of pharmaceutical production equipment, including autoclaves, process tanks, filtration systems, and CIP/SIP systems.

• Aseptic processing and sampling techniques.

• Media and buffer preparation.

• Cleanroom manufacturing practices and controlled environment operations.

• Process monitoring and critical parameter documentation.

• Process troubleshooting in regulated manufacturing environments.

• Process/equipment validation support.

• Basic knowledge of microbiology, chemistry, sterility, and lyophilization related to biopharmaceutical manufacturing.

• Experience in biopharmaceutical or pharmaceutical manufacturing environments.

• Knowledge of supplier/customer process flows and manufacturing interdependencies.

• Experience with manufacturing documentation control and work order management.

• Participation in continuous improvement projects.

• Scientific degree or related scientific background.

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