Technician IV
MSCCN - Ashland, OH
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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. Job Summary A Technician IV has substantial knowledge in the basic skills and study designs and can perform the intermediate skills and procedures of the department training plan. The technician is assigned to work on study, performing tasks independently which may include performing intermediate or some advanced dose routes, clinical observations, animal handling and restraint, blood collection, data collection/recording to support each skill, support after-hours activities, and serving as a lead technician for basic and complex studies. The technician will begin to be assigned to more advanced tasks that may include working with additional species, and/or specialized procedures to support the study needs. ESSENTIAL DUTIES AND RESPONSIBILITIES : Ensure good welfare and humane care for all animals worked with through gentle, positive human- animal interactions. Perform intermediate or some advanced dose routes, clinical observations, animal handling and restraint, blood collection, data collection/recording to support each skill, support after-hours activities, and serving as a lead technician for basic and complex studies. Specific tasks will be based on each area's training plan and business needs. Assist with advanced tasks of the department. Collect, document, review, and verify data on forms, or in electronic data capture systems. Ensure high levels of study quality to meet study goals. Maintain appropriate communication with other personnel. Support team-mates, technicians, and members of other departments. Follow direction from team leaders, trainers, research associates and supervisors. Use and maintain instrumentation and equipment according to SOPs. Perform all tasks per SOP, BOP, and protocols. Perform all other related duties as assigned. Job Qualifications Education: High school diploma or General Education Degree (G.E.D.) preferred. Experience: 2-3 years of relevant 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 recommended. Skill plan completed for this role based on department training plan. Demonstrated ability to consistently and effectively produce high quality results, interpret protocol requirements, troubleshoot quality issues, and record accurate study and departmental data. Ability to communicate verbally and in writing at all levels inside and outside the organization. Ability to manage multiple tasks and priorities to achieve goals. Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system. Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of. Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules. Ability to exercise independent decision-making and self-manage under the direction of a supervisor. Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice. Ability to work under specific time constraints. 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 supported the development of 86% of the drugs approved by the FDA in 2021. Equal Employment Opportunity Charles 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, 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 . 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 224522
Created: 2024-09-12