Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. **Hours:** 2nd Shift; 1300 - 2330, Monday-Thursday, 10 hours Clayton The incumbent is responsible for performing complex laboratory analysis of plasma and plasma products in a GMP laboratory. Responsibilities include sample accessioning, sample preparation, reagent preparation, testing, result calculation, as well as qualitycontrol of assays and equipment. The incumbent will also support assay validation, method transfer, reagent and control qualification, and laboratory maintenance activities as assigned. Must be comfortable working with infectious material on a dailybasis. Person must be able to work in a biological safety cabinet and comfortable working with a microscope for several hours at atime. Candidates for the position must be proficient with using micropipettes and serological pipettes while making dilutions andserial dilutions. Must be able to perform tasks by following SOP’s and oral instructions. Must have precise, legible, and organized documentation skills. Candidates must also be willing to perform their share of cleaning duties and housekeeping. This position is responsible for performing bioburden and endotoxin testing of in-process product samples and raw materials tosupport plasma production processes, including process and equipment activities. The Quality Control Sterility & Microbiology department must maintain adequate staffing to support all production operations 24 hours per day, 7 days a week. In addition to in-process product monitoring, this position may also assist with environmental monitoring of production and testing areas. Thisposition is part of the budgeted staff necessary to complete this sampling and testing and to ensure that Clayton site productionprocesses and production areas remain in a state of control. **Assistant Level:** Associates Degree in a life science field, medical technology, or related curriculum and a minimum of six months of applicable laboratory experience or a BS/BA degree in a life science field, medical technology, or related curriculum is required. A background in medical technology/clinical laboratory science is preferred, as is experience in a GLP/GMP laboratory. Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/ orcompetencies may be considered in place of the stated requirements. **Associate Level:** The Associate Biologist position is normally a progression from the Assistant Biologist position in the QualityControl Biology Labs. Therefore, the Associate Biologist position also requires knowledge equivalent to a minimum of two years of college level biology courses (one year of general biology course(s) with associated laboratory work, and one year of microbiology course(s) with associated laboratory work). While the content of the course work specified above is generally applicable to theAssistant Biology position, the associated laboratory experience is more specifically applicable to the position's work assignments. Abackground in medical technology/clinical laboratory science is preferred, as is experience in a GLP/GMP laboratory. Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Work is performed in an office and a laboratory/manufacturing environment. Exposure to biological fluids with potential exposure toinfectious organisms. Exposure to occasional extreme cold below 320C in production areas. Exposure to electrical office andlaboratory equipment. Personal protective equipment required such as protective eyewear, garments and gloves. Work is performedsitting or standing for 2-4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movementsof the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects.Light to moderate lifting and carrying objects with amaximum lift of 35lbs. Occasionally walks, bends and twists neck and waist,may reach above or below shoulder height. Frequent foot movements. Color perception/discrimination and near vision correctable inone eye to 20/30 and to 20/100 in the other eye. Able to communicate complex information and ideas so others will understand;with the ability to listen to and understand information and ideas presented through spoken and written words and sentences.Performs tasks by following a set of written or oral instructions/procedures. ***Employee Referral Bonus Eligible*** Learn more about Grifols \#LI-YR1 Third Party Agency and Recruiter Notice: Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate. **Grifols provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other characteristic or status protected by law.** **We will consider for employment all qualified Applicants, including those with Criminal Histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance.** Learn more about Grifols (https://www.grifols.com/en/what-we-do) **Req ID:** 519877 **Type:** Regular Full-Time **Job Category:** Quality