Health Care

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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. POSTION SUMMARY Under the supervision of the Facility Manager and/or Operations Manager, you will be responsible for assisting with the daily management of operations of the donor center, supervising operations and quality control, and ensuring compliance with all applicable policies and regulations. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.Responsible for all aspects of the donor facility when the Facility Manager is not present.Perform any/all tasks within the plasma center; train production employees and demonstrate how tasks are to be performed to meet company standards, and on occasion, fulfill the role of production employees when the need arises.There will be many occasions when you will be the manager of the donor center, up to 40 hours/week or more. Create appropriate organizational environment and value systems which stimulate the morale and productivity of the work force and its leadership.Provide strategic direction, planning, and customer focus. Develop action plans to improve operations and supervise the implementation of improvements.You will be required to facilitate internal and external audits.Supervise donor selection, plasma collection, and all manufacturing records to maintain the highest production standards in accordance with Federal and State regulations, with FDA approved Standard Operating Procedure manual, OSHA, CLIA, and cGMP, through systems in place and via Quality Supervisor. Responsible for all personnel functions including hiring, development and training, disciplinary actions and termination, and maintenance of all personnel records.Determine adequacy of inventory of all goods and supplies necessary for center operation and oversee ordering goods as needed.Assure that subordinates maintain the facility in a neat and clean condition and all equipment is kept in good working order.Submit timely and accurate reports on a daily/weekly and monthly basis or when requested.Develop and implement active donor recruitment advertising campaign to improve production levels.Control center donor funds and ensure that all financial records are accurate and in order.Keep immediate superior informed of any irregularities within the center and provide action plans to improve and correct center deficiencies.Minimize center liability through constant risk management review.Signed Statement of Responsibility and Curriculum Vitae on file at the center and Authorized Official’s office. REQUIRED EDUCATIONAL QUALICATIONSTo 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, and/or ability required. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. College Degree (unless waived by senior management of Biomat USA, Inc.).Evaluation and/or translation of any foreign education (high school, university, or professional training) must be provided.  REQUIRED EXPERIENCE/SKILLS One (1) year plasma experience, including six months experience as an Operations Supervisor.Must have legible handwriting.Must be able to read, write, and speak English.Must be able to use a computer. PHYSICAL REQUIREMENTS: Ability to travel via automobile and/or airplane.Ability to stand for extended periods of time – up to four (4) hours at a time.Ability to view video display terminal less than 18” away from face – up to four (4) hours a time.Ability to lift, tug, pull up to fifty (50) pounds.Ability to handle mental stress.Submitting 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=217492&company_id=16052&jobboardid=1764 We are an Equal Opportunity Employer