Technologist IVB

About the role

Perform various laboratory procedures in compliance with CGMP regulations as they apply to the conduct of nonclinical research.

Responsibilities

• Perform daily test article/substance administration, observation and recording of physical signs of species for contracted laboratory studies.
• Prepare cage tags and individual animal number tags; prepare and autoclave cages.
• Prepare data forms for routine study procedures.
• Auxiliary in preparation of data forms for specialized study procedures.
• Record study parameters as required by protocol.
• Ensure adequate supply of dosage equipment during the course of study.
• Auxiliary in ensuring adequate supply of additional study specified materials such as blood collection tubes.
• Auxiliary in preparation of test agents.
• Generate periodic summarization of data.
• Ensure raw data records are accurate, complete, and in appropriate order, and meet protocol specifications and/or GCGMP requirements.
• Auxiliary in interaction with project managers and technical staff in planning and conduct of studies.
• Auxiliary in planning and coordinating the activities of the department through hands-on technical support, communication with animal production / lab personnel and occasional delegation to other animal production / lab personnel.
• Share responsibility for maintaining appropriate inventory levels of departmental supplies.
• Responsible for proficiency in all departmental SOPs with general knowledge of the lab/production processes.

Requirements

• Education: Associate's degree (A.A /AS.) or equivalent in Biological Sciences or related discipline.
• Experience: One to two years related technical experience.
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Certification/Licensure: ALAT certification preferred.

Qualifications

• Bachelor's degree preferred.

Benefits

The pay for this position is $24.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

About Biologics Testing Solutions

With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.

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. 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.