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Technologist - In-Vivo Biologics
Charles River Laboratories International Inc (CRL)
Wilmington, MA, US, 01887
Basic Summary
Below are the responsibilities of the Technologist role for our IVB department in Wilmington, MA
- 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. Assist with 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. Assist in ensuring adequate supply of additional study specified materials such as blood collection tubes.
- Assist 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.
- Assist in interaction with project managers and technical staff in planning and conduct of studies.
- Assist 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.
- Perform all other related duties as assigned.
Minimum Qualifications
- Associate’s degree (A.A. /A.S.) or equivalent in Biological Sciences or related discipline.
- One year 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.
Compensation Data
The pay range for this position is $23 an 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 supported the development of 86% of the drugs approved by the FDA in 2021.
Equal Employment OpportunityCharles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin, veteran or disability status.
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.
Job posted: 2023-05-11
