• GMP Manufacturing Technician

    Astrix Technology (Los Angeles, CA)


    GMP Manufacturing Technician

     

    Manufacturing

     

    Los Angeles, CA, US

    Pay Rate Low: 24 | Pay Rate High: 26

    + Added - 28/07/2025

     

    Apply for Job

     

    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

     

    We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.