Immunopathology Analyst I

About the role

We are seeking an Immunopathology Analyst I for our Safety Assessment site located in Reno, NV.

Responsibilities

• Generate and record data with minimal supervision in the performance of studies.
• Handle and process samples and perform accurate data collection and reporting.
• Perform laboratory tasks by various basic methods.
• Inputs, prints, and edits laboratory data entries.
• Prepares materials and data for shipment and archiving.
• Receives samples and complete tracking documentation.
• Reviews documentation of functions performed as part of quality control requirements.
• Performs study preparation activities including label printing, sample labeling, reagent labeling, bulk reagent preparation, equipment verifications, sample labeling and equipment verifications.
• Maintains clean work areas.
• Performs all other related duties as assigned.

Requirements

• Education: Bachelor’s degree (B.A. / B.S) or equivalent in laboratory science or related discipline required.
• Experience: None.
• Certification/Licensure: None.

Qualifications

• Must be able to perform effectively as a team member.
• Must be able to accurately record data.
• Must be able to follow verbal and written instructions.
• Must be able to communicate effectively.
• Must be able to interact in a professional manner with management, coworkers, and sponsors.
• Must be able to quickly learn and utilize computer programs as needed; previous computer experience preferred.

Skills

• Experience in biology, chemistry/pharmacy, or similar lab environment preferred.
• Previous experience in GLP environment preferred.

Pay

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.

Schedule

N/A

Benefits

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.

About Safety Assessment

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.

About Charles River

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. 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. 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. We’re committed to providing benefits that elevate your quality of life.

Equal Employment Opportunity

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. 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. 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. For more information, please visit www.criver.com.