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Immunopathology Analyst I (Reno, NV, US, 89511)

Charles · Reno, NV, US, 89511
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posted
1d ago
location
Reno, NV, US, 89511
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<p><span style="font-size:10.0pt"><span style="font-family:Arial, Helvetica, sans-serif">For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.</span></span></p><div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:16.0px;word-wrap:break-word"><H2 style="font-size:1.0em;margin:0.0px"><b>Job Overview</b></H2> </div><div><p><span style="font-size:10.0pt">We are seeking an <strong>Immunopathology Analyst I </strong>for our <strong>Safety Assessment</strong> site located in <strong>Reno, NV</strong>. </span></p> <p> </p> <p><span style="font-size:10.0pt">Generate and record data with minimal supervision in the performance of studies. Responsible for handling and processing samples and performing accurate data collection and reporting. Perform laboratory tasks by various basic methods.</span></p> <p> </p> <p><strong><span style="font-size:10.0pt">ESSENTIAL DUTIES AND RESPONSIBILITIES: </span></strong><br><span style="font-size:10.0pt">•    Performs immunohistochemistry and tissue cross reactivity in support of the immunopathology laboratory procedures and collect and record/document research data in compliance with Good Laboratory Practices (GLPs), Standard Operation Procedures (SOPs), study protocols and company policies/practices. </span><br><span style="font-size:10.0pt">•    May act as lead/primary technician on basic studies while under supervision.  </span><br><span style="font-size:10.0pt">•    Inputs, prints, and edits laboratory data entries. </span><br><span style="font-size:10.0pt">•    Prepares materials and data for shipment and archiving. </span><br><span style="font-size:10.0pt">•    Receives samples and complete tracking documentation. </span><br><span style="font-size:10.0pt">•    Reviews documentation of functions performed as part of quality control requirements.</span><br><span style="font-size:10.0pt">•    Performs study preparation activities including label printing, sample labeling, reagent labeling, bulk reagent preparation, equipment verifications, sample labeling and equipment verifications. </span><br><span style="font-size:10.0pt">•    Maintains clean work areas.</span><br><span style="font-size:10.0pt">•    Performs all other related duties as assigned.</span></p></div></div><div style="padding:10.0px 0.0px;border:1.0px solid transparent"><div style="font-size:16.0px;word-wrap:break-word"><H2 style="font-size:1.0em;margin:0.0px"><b>Job Description</b></H2> </div><div><p> </p> <p><span style="font-size:10.0pt">•    <span><strong>Education:</strong></span> Bachelor’s degree (B.A. / B.S) or equivalent in laboratory science or related discipline required.</span><br><span style="font-size:10.0pt">•    <span><strong>Experience:</strong></span> None.</span><br><span style="font-size:10.0pt">•    An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.</span><br><span style="font-size:10.0pt">•   <span><strong> Certification/Licensure:</strong></span> None</span><br><span style="font-size:10.0pt">•    <span><strong>Other: </strong></span>Must be able to perform effectively as a team member, accurately record data, follow verbal and written instructions, communicate effectively, and interact in a professional manner with management, coworkers, and sponsors.</span><br><span style="font-size:10.0pt">•    Must be able to quickly learn and utilize computer programs as needed; previous computer experience preferred.</span></p> <p> </p> <p><span style="font-size:10.0pt"><strong>PREFERRED QUALIFICATIONS:</strong></span><br><span style="font-size:10.0pt">•    Experience in biology, chemistry/pharmacy, or similar lab environment preferred. </span><br><span style="font-size:10.0pt">•    Previous experience in GLP environment preferred. </span></p> <p> </p> <p><span style="font-size:10.0pt"><strong>The pay for this position starts at $24/hr.  Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.</strong></span></p></div></div></div><p><span style="font-size:10.0px"><span style="font-family:Arial, Helvetica, sans-serif"><b>About Safety Assessment</b><br> Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market.  Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.</span></span></p> <p><br> <span style="font-size:10.0px"><span style="font-family:Arial, Helvetica, sans-serif"><b>About Charles River</b><br> Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.</span></span></p> <p><span style="font-size:10.0px"><span style="font-family:Arial, Helvetica, sans-serif">With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.</span></span></p> <p><span style="font-size:10.0px"><span style="font-family:Arial, Helvetica, sans-serif">At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.</span></span></p> <p><span style="font-family:Arial, Helvetica, sans-serif"><span style="font-size:10.0px"><span><span style="color:#333333">We’re committed to providing benefits that elevate your quality of life.  Based on your position these may include:  bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.</span></span></span></span></p> <p> </p> <p><span style="font-size:10.0px"><span style="font-family:Arial, Helvetica, sans-serif"><b>Equal Employment Opportunity</b></span></span></p> <p><span style="font-size:10.0px"><span style="font-family:Arial, Helvetica, sans-serif">Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.</span></span></p> <p><span style="font-size:10.0px"><span style="font-family:Arial, Helvetica, sans-serif">It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.</span></span></p> <p><span style="font-size:10.0px"><span style="font-family:Arial, Helvetica, sans-serif">If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.</span></span></p> <p> </p> <p><span style="font-size:10.0px"><span style="font-family:Arial, Helvetica, sans-serif">For more information, please visit www.criver.com.</span></span></p>