• Sr. Biopharmaceutical Manufacturing Associate

    Astrix Technology (Agoura Hills, CA)


    Sr. Biopharmaceutical Manufacturing Associate

     

    Manufacturing

     

    Agoura Hills, CA, US

    Pay Rate Low: 30 | Pay Rate High: 34

    + Added - 16/10/2025

     

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    Position Overview

    We are seeking an experienced quality and operations professional to drive excellence in our biopharmaceutical manufacturing environment. This role focuses on quality system management, process optimization, and cross-functional collaboration to ensure operational compliance and continuous improvement. The position requires initial full-time onsite presence with flexibility for remote work after the training period.

     

    **Location:** Agoura Hills, CA (Hybrid - Initial onsite period required)

    **Pay** : $30-$34/hour

    **Type** : Contract

    **Hours** : M-F 8-5

    Key Responsibilities

    + Oversee quality investigation processes and improvement action plans from initiation through closure, ensuring adherence to established timelines and documentation standards.

    + Apply structured project coordination approaches to track, prioritize, and communicate status of quality initiatives and improvement activities.

    + Partner with cross-functional teams including technical operations, quality assurance, process development, regulatory affairs, and external vendors.

    + Maintain compliance with industry regulations and internal operating procedures governing pharmaceutical manufacturing.

    Required Qualifications

    **Education & Experience** (one of the following combinations):

    + Graduate degree with 2+ years in pharmaceutical/biotech manufacturing or operations

    + Bachelor's degree with 3+ years in pharmaceutical/biotech manufacturing or operations

    + Associate degree with 5+ years in pharmaceutical/biotech manufacturing or operations

    + High school diploma/equivalent with 10+ years in pharmaceutical/biotech manufacturing or operations

    **Technical background** in life sciences, engineering, or related discipline

    Preferred Qualifications

    + Familiarity with quality management system platforms for pharmaceutical operations.

    + Demonstrated analytical capabilities with strong root cause analysis and resolution skills.

    + Understanding of current Good Manufacturing Practice (cGMP) requirements.

     

    _This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!_

    _\#INDBH_

    _\#LI-DNP_

    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.