Health Care

applicants

Biomat USA, Inc., a part of the global Grifols family of companies, specializes in the collection of plasma for use in life-saving therapies. Biomat USA, Inc. , along with PlasmaCare, Inc., have a network of over 80 plasmapheresis donor centers throughout the United States. These state-of-the-art facilities collect plasma from donors and operate according to the highest standards of quality. For moreinformation, please visit our website at http://biomatusa.grifols.comUnder the supervision of the Director of Quality, ensure donor centers in region operate within established processes to assure the product meets or exceeds all quality standards set forth in regulatory, client and company requirements. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.1. Direct supervision of center Quality Supervisors including hiring, training and development, discipline and termination. 2. Visit centers as needed and routinely interact with the Quality Supervisor to monitor all established quality activities in place. Ensure that they are effective, feasible and continue to produce desired results; recommend corporate wide improvements. 3. Assure compliance with SOPs and that SOP revisions are implemented correctly. 4. Interact with center Quality Supervisor and center management to develop corrective actions for inspectional findings and assure they are implemented and effective. 5. Assure that required proficiency testing is performed and reported accurately. 6. Interact with the Quality Supervisors to assure Error Management activities and reporting are handled appropriately. - Evaluate adequacy of corrective actions and completeness of reports, assist in root cause analysis.- Investigate and propose additional corrective actions as required. - Monitor compliance of corrective actions where indicated through various systems in place.7. Monitor and analyze customer complaints, QA Tracking and QA Trending errors, external audit findings, and internal audit findings; recommend and implement corporate wide corrective actions 8. Supply technical information to external and internal customers. 9. Other assignments as directed by the Director of Quality.1. Undergraduate degree in one of the allied sciences (chemistry, biology, or medical technology) or professional equivalent, such as R.N or Medical Technologist unless waived by senior management in the Biologics Division. . Evaluation and/or translation of any foreign education (high school, university, or professional training) must be provided.Ability to operate a computer keyboard and calculator. Ability to articulate clearly and conduct oral presentations. Must have legible handwriting.Ability to read and write the English Language. PHYSICAL REQUIREMENTS1. Ability to travel via automobile and/or airplane as needed.2. Ability to view video display terminal less than 18' away from face for extended periods of time. 3. Ability to lift, pull, tug up to twenty (20) pounds. 4. Ability to articulate clearly.2. Two (2) years experience in a laboratory, drug manufacturing, medical device or in-vitro diagnostic industry, unless waived by senior management in the Biologics Division. 3. Previous work experience should demonstrate good interpersonal, written and verbal communication skills, self-motivation, and ability to perform tasks with minimal supervision.Closing Date to Apply is by October 27, 2010Submitting 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=218094&company_id=16052&jobboardid=1764 We are an Equal Opportunity Employer