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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
* Bachelors 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.
Full Time
$69k-84k (estimate)
06/26/2024
07/09/2024
oakwoodlabs.com
OAKWOOD VILLAGE, OH
50 - 100
Private
EDWARD C SMITH
$10M - $50M
Pharmaceutical