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Our client, a renowned leader in the field of biotechnology, is revolutionizing the use of living cells to create groundbreaking biologic medicines. As a guiding force in the biotech industry, they set the bar for innovation and advancement. Job Title: GMP Manufacturing Process Technician (Contract-to-Hire) Schedule: Onsite | Monday-Friday, 8:00 AM - 5:00 PM Pay Rate: $24 - $26 per hour Overview A leading biotechnology organization is seeking a GMP Manufacturing Process Technician to join their Synthetic Manufacturing and Clinical Supply team. This role will be based onsite at their pilot-scale drug product manufacturing facility and formulation development lab in Thousand Oaks, CA. The technician will support both non-GMP and GMP manufacturing activities for early-phase clinical pipeline synthetic drug products, primarily solid dosage forms. Key Responsibilities Execute manufacturing unit operations such as blending, granulation, roller compaction, drying, milling, compression, encapsulation, and film coating. Support manufacturing process readiness activities and assist in preparing batch records for GMP campaigns. Perform visual inspection of drug products and ensure adherence to quality standards. Handle dispensing and management of hazardous raw materials while following safety protocols. Conduct hands-on equipment cleaning, sanitization, and setup for manufacturing processes. Maintain equipment and facility documentation, including logbooks and inventory of raw materials and consumables. Collaborate closely with cross-functional teams including process development chemists, engineers, and analysts. Recommend and implement process improvements to enhance efficiency and compliance. Qualifications Basic Requirements: High school diploma/GED with 1+ year of relevant work or military experience, OR Associate degree. Preferred Skills/Experience: Familiarity with GMP compliance, documentation practices, and manufacturing unit operations for synthetic drug products. Experience with solid dosage drug product processes (granulation, blending, tablet compression, etc.). Strong teamwork skills and ability to collaborate in a cross-functional environment. Comfort working with complex machinery and hazardous materials while adhering to safety requirements. Why Join? Opportunity to work with a dynamic team supporting innovative clinical drug development. Hands-on experience in a pilot-scale drug manufacturing facility. Potential for contract extension and growth within the organization. INDBH