applicant
Plasma Clearing Inspector (217078-052) - City of Industry, CA 91746
at Grifols, Inc. in City of Industry, CA
Grifols has been a leader in the healthcare industry since 1940 by creating innovative products and services based on the values of ethics, quality and responsibility. Grifols' activities focus on fulfilling the needs of its patients as well as healthcare professionals working in therapeutics, pharmacy, diagnostics and blood banking. For more than 60 years, Grifols has developed, manufactured and marketed products designed to improve human health. At its Los Angeles facility, Grifols manufactures plasma derived biopharmaceutical products of proven efficacy, quality and safety. Since 2001 , Grifols has acquired 80 plasmapheresis donor centers within the USA. The donor centers derived from the following companies: Biomat USA, Inc. with 60 donor centers, Plasma Collection Centers, Inc ., (PCCI) with 4 donor centers and Plasmacare, Inc. with 16 donor centers. These state of the art facilities collect human plasma from paid donors to create life-saving pharmaceutical products such as clotting factors, immunoglobulin and albumin for patients who suffer from bleeding disorders, immune system deficiencies, burns and shock. For more information, please visit our website: http://biomatusa.grifols.com. Biomat USA Plasma Clearing Inspector Grifols has been a leader in the healthcare industry since 1940 by creating innovative products and services based on the values of ethics, quality and responsibility. Grifols' activities focus on fulfilling the needs of its patients as well as healthcare professionals working in therapeutics, pharmacy, diagnostics and blood banking. For more than 60 years, Grifols has developed, manufactured and marketed products designed to improve human health. At its Los Angeles facility, Grifols manufactures plasma derived biopharmaceutical products of proven efficacy, quality and safety. Since 2001, Grifols has acquired 80 plasmapheresis donor centers within the USA. The donor centers derived from the following companies: Biomat USA, Inc. with 60 donor centers, Plasma Collection Centers, Inc., (PCCI) with 4 donor centers and Plasmacare, Inc. with 16 donor centers. These state of the art facilities collect human plasma from paid donors to create life-saving pharmaceutical products such as clotting factors, immunoglobulin and albumin for patients who suffer from bleeding disorders, immune system deficiencies, burns and shock. For more information, please visit our website: http://biomatusa.grifols.comPosition Summary:Position requires scanning and removal of unsuitable plasma units utilizing the Plasma Management System (SGP). A visual inspection of plasma units is also performed, removing any units which are unacceptable (e.g. damaged, broken port/tube, red blood cells off, or backup sample rejections).Job Responsibilities: (include the following. Other duties may be assigned)Responsible for scanning bottles of frozen plasma units assigned to a Production Unit (PU) utilizing a barcode readerResponsible for transferring unit to a sub-shipment during the PU processResponsible for entering “statistics” during the PU processResponsible for transferring units between PU’sResponsible for “blocking” of units which do not meet customer requirementsResponsible for various rejections found during visual inspectionResponsible for removal of unsuitable plasma units per “Removal Requests” during any step of the plasma process.Cross train in operating Automatic Conveyor System (e.g. startup, end of shift, alarms, robot)Maintain record accountabilityResponsible for monitoring plasma time out of freezerResponsible for department housekeeping and safety practicesSkills/Qualifications/Education: (To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions).High school diploma or equivalent is requiredOne year of experience in a manufacturing, pharmaceutical, or other FDA regulated industry is desirableKnowledge of cGMPs and Industry StandardsAbility to follow written procedures – “Standard Operating Procedures”Possess good verbal and written communication skillsPossess basic math skills (addition, subtraction, division, multiplication)Basic computer skills requiredAbility to perform job duties with minimum supervisionAbility to lift 25 lbs. repeatedlyAbility to perform repetitive functions with high level of concentrationAbility to stand for prolonged periods of timeSubmitting a resume online at a job site could cause valuable screening information to be missed.Please apply directly at: http://hostedjobs.openhire.com/epostings/submit.cfm?fuseaction=app.dspjob&jobid=217078&company_id=16052&jobboardid=1764 We are an Equal Opportunity Employer
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