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Solon

    Quality Assurance Documentation Specialist - Solon, United States - Oakwood Labs

    Oakwood Labs
    Oakwood Labs Solon, United States

    2 weeks ago

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    Description

    Job Description

    Job Description

    This position is an excellent opportunity for a quality minded individual interested in working in a technology- based pharmaceutical company.

    Essential job functions include:

    • Generate, issue, reconcile, and archive batch records, protocols logbooks, and other controlled documents,
    • Perform batch record review and work with various department to resolve and correct errors and ensure Good Documentation Practices are followed,
    • Administer the electronic document, quality, and training management systems,
    • Assist during all phases of the change management process,
    • Processes and provides oversight of submitted change requests,
    • Provides oversight of all routine reviews of documentation,
    • Provides routine communications to the various departments and customers on outstanding tasks associated with the with the document control and change management process.

    Attributes for the position:

    • Prior experience in quality systems preferred
    • Prior experience in pharmaceutical, GMP, or ISO manufacturing environment preferred
    • Bachelor's Degree in a science related field or equivalent experience

    Oakwood Labs is a privately owned specialty pharmaceutical company focused on the design, development, and commercial manufacture of sterile injectable sustained- release microsphere products. This unique class of medications delivers therapeutic levels of drug to patients over days, weeks, months, or a year with a single intramuscular or subcutaneous injection. Products of this class have extremely high commercial potential.


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