This job is currently Archived,
Posted on : 13 May 2017
BioMarin is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases. We target diseases that lack effective therapies and affect relatively small numbers of patients, many of whom are children. These conditions are often inherited, difficult to diagnose, progressively debilitating and have few, if any, treatment options. BioMarin will continue to focus on advancing therapies that are the first or best of their kind. The incumbent will provide logistical and documentation support for the QC Product department at BioMarin. Responsibilities include a variety of administrative and documentation support tasks.The incumbent will perform tasks per Standard Operating Procedures (SOP), Good Laboratory Practice (GLP), and current Good Manufacturing Practice (cGMP). Good reading and writing skills are essential. Must have a service oriented attitude, display initiative, and be able to fulfill responsibilities with minimal supervision.- file test records generated by QC analysts- compile paperwork and generate lot release and stability reports- track and file miscellaneous studies generated by QC- archive QC documentation and keep an accurate inventory of records on and off site- ensure that documents will be stored so that they are readily available for authorized inspections- order office supplies and maintain a suitable inventory to perform administrative tasksAn AA in a biological or chemical science is preferred. Some laboratory or GMP experience is desirable but not essential.#LI-DNI 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.
Find a Job Find Candidates