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  • Quality Assurance Specialist I (MQA)

    Genentech (Hillsboro, OR)



    Apply Now

    The Position

    Hillsboro Technical Operations (HTO) is a drug product & finished goods manufacturing organization responsible for the reliable delivery of Roche’s commercial portfolio & pipeline products. The Quality organization at HTO comprises Quality Assurance, Quality Systems & Compliance, Quality Control, and Quality Engineering & Validation. Together, we produce millions of units of life-saving medicine every year to patients around the world.

     

    The Opportunity

     

    In this exciting role, you will be part of the Frontline Team in the Manufacturing Quality Assurance. You will contribute to core Quality tasks by providing essential support for manufacturing activities, documentation review, and initial discrepancy support. You will learn to partner effectively with cross-functional stakeholders at the site.

     

    + You will provide basic Quality Assurance support for routine GMP activities in manufacturing at HTO.

    + You will partner with experienced team members to provide floor support, initial batch record review steps, and discrepancy management (Quality Incidents and Minor Deviations).

    + You will resolve routine Quality Assurance issues limited in scope and complexity following cGMP regulations.

    + You will execute daily tasks and complete documentation review with low to moderate supervision.

    + You will collaborate cross functionally to ensure that all review activities are executed efficiently and effectively.

    + You will support Quality process improvement initiatives by contributing data collection or assisting with minor tasks as directed.

    Who you are:

    + You hold a B.A./B.S. degree (preferably in Life Science) with 1-3 years of relevant experience in a regulated environment, or an equivalent combination of education and experience.

    + You are able to perform physical activity including, but not limited to lifting, standing for periods of time, and gowning.

    + You have basic knowledge or familiarity with cGMPs or equivalent regulations.

    + You have experience or a strong aptitude for reviewing documentation with high attention to detail.

    + You are able to learn to interpret and relate Quality standards for implementation and review.

    + You are able to evaluate situations and propose potential solutions.

    + You are able to communicate clearly and professionally both in writing and verbally.

    + You have a flexible and adaptable approach to problem solving, learning new tasks and meeting business objectives.

     

    The expected salary range for this position based on the primary location for this position of Hillsboro, OR is $55,000 - $102,000. Actual pay will be determined based on experience, level, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.

     

    Please note this role is eligible for relocation benefits.

     

    Link to Roche/Genentech Benefits (http://yourlifeyourrewards.com/)

     

    Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

     

    If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants (https://docs.google.com/forms/d/e/1FAIpQLSdZWlsbfQOvFVIQgHE\_iDzWUTlhZvj6FytIzjS7xq6IGh1H5g/viewform) .

     


    Apply Now



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    Genentech (Hillsboro, OR)
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