Manufacturing Associate

The Fountain Group is currently seeking a Manufacturing Associate for a prominent client of ours. This position is in Newbury Park, CA 91320. Details of the position are as follows: 

Job Description:

• Pay: $28.26/hr - $29.23/hr based on experience.
• 6-month assignment with the possibility for extension or conversion based on performance and budget.

• Swing Shift: Sunday – Wednesday, 12:00 PM – 10:30 PM.
• Execute manufacturing processes while strictly adhering to cGMP, GDP, environmental health and safety guidelines, and all applicable regulations.
• Clean, set up, operate, and tear down manufacturing equipment including tanks, filtration systems, and production equipment.
• Perform room sanitization and maintain equipment in GMP-compliant condition.
• Complete manufacturing documentation and batch records following GDP/GMP guidelines.
• Prepare media and buffer solutions and perform sampling using aseptic techniques.
• Operate production equipment such as pH meters, conductivity meters, autoclaves, and portable mixers.
• Monitor, record, and document critical process parameters.
• Receive and distribute production supplies and materials as needed.
• Support document control activities, work order generation, and process/equipment validation efforts.
• Troubleshoot manufacturing issues and identify appropriate corrective actions.
• Participate in continuous improvement initiatives and cross-functional projects.
• Perform routine maintenance and cleaning of production equipment.
• Work in controlled cleanroom environments requiring strict gowning procedures and PPE.
• Collaborate with manufacturing and support teams to ensure adherence to production schedules.
• Work overtime, weekends, holidays, or alternate shifts as business needs require.

Qualifications:

• High School Diploma/GED with 4+ years of related experience OR an AA Degree with 2+ years of related experience OR a Bachelor's Degree is required.
• Prior experience in a GMP-regulated pharmaceutical, biotechnology, or manufacturing environment is required.
• Must have knowledge of cGMP and Good Documentation Practices (GDP).
• Must be willing and able to wear required PPE and follow gowning requirements, including protective clothing covering the head, face, hands, feet, and body.

Preferred Qualifications:

• Experience working in a cleanroom environment.
• Experience with aseptic techniques and pharmaceutical manufacturing processes.
• Knowledge of microbiology, chemistry, sterility, or lyophilization.
• Experience operating laboratory or pharmaceutical production equipment such as autoclaves, process tanks, incubators, pH meters, and conductivity meters.
• Experience with batch record documentation, validation activities, and process troubleshooting.
• Strong teamwork, communication, problem-solving, and continuous improvement experience.

Working Environment:

• Controlled cleanroom environment requiring special gowning and PPE.
• No makeup, jewelry, contact lenses, nail polish, or artificial fingernails permitted in manufacturing areas.
• Frequent interaction with team members in a highly regulated pharmaceutical manufacturing setting.
• Pace may be fast and job completion demands may be high.

If you are interested in hearing more about the position, please respond to this post with your resume attached or contact me at (813) 600-3536

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