Charles River
Associate Director Environmental Health and Safety
Charles River, Nashville, Tennessee, United States
Job Summary
Acts as the Environmental, Health & Safety subject matter expert responsible for the oversight of all EHS&S programs with the goal of ensuring EHS&S compliance of the CRL Memphis facilities. Develop and aid departments in the implementation of policies and procedures targeted toward increasing personnel safety and protection of the environment. Work with Memphis and Corporate employees to continue to create and sustain a proactive safety culture where EHS&S is built into operations. Develop and implement Memphis EHS&S inspection program using Enablon, the CRL EHS&S management system. Support the corporate EHS&S assessment team in their assessment of the Memphis site. Manage the closure of all findings discovered. Report and work directly with the Site Director with a dotted line to the EHS&S Business Partner of Manufacturing. Participate as a member of the Site Leadership Team(s) and conduct reviews at appropriate intervals with facility senior management Ensure proper training programs are available and assigned to the appropriate employees with regards to environmental, health, and safety compliance. Job Qualifications
Education: Bachelor’s degree (B.A./B.S.) or equivalent in a life science (biology, chemistry), environmental engineering, or related discipline. Experience: Ten to 15 years related experience in a regulated environment. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above. Certification/Licensure: Preferred but not required: CSP, CIH, and/or other EHS credential. The pay range for this position is $145,700 - $161,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. About Charles River’s CDMO Services
With over 20 years of experience and industry-leading expertise, Charles River’s cell and gene therapy Contract Development and Manufacturing Organization (CDMO) group supports biotechnology and pharmaceutical companies in advancing their complex programs from early development through commercialization. Our integrated, phase-appropriate CDMO capabilities—including plasmid DNA, viral vector, and cell therapy manufacturing—enable seamless development and faster timelines. With centers of excellence in the US and UK, we offer GMP-compliant and research-grade solutions, along with comprehensive analytical services and regulatory support. Whether clients need end-to-end development, standalone services, or insourced support, our CDMO team provides custom solutions to meet evolving program needs. From process development in Hanover to viral vector manufacturing in Rockville, large-scale cell therapy production in Memphis, and plasmid DNA services in Keele, we simplify the supply chain and accelerate cell and gene therapy breakthroughs. About Charles River
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.
#J-18808-Ljbffr
Acts as the Environmental, Health & Safety subject matter expert responsible for the oversight of all EHS&S programs with the goal of ensuring EHS&S compliance of the CRL Memphis facilities. Develop and aid departments in the implementation of policies and procedures targeted toward increasing personnel safety and protection of the environment. Work with Memphis and Corporate employees to continue to create and sustain a proactive safety culture where EHS&S is built into operations. Develop and implement Memphis EHS&S inspection program using Enablon, the CRL EHS&S management system. Support the corporate EHS&S assessment team in their assessment of the Memphis site. Manage the closure of all findings discovered. Report and work directly with the Site Director with a dotted line to the EHS&S Business Partner of Manufacturing. Participate as a member of the Site Leadership Team(s) and conduct reviews at appropriate intervals with facility senior management Ensure proper training programs are available and assigned to the appropriate employees with regards to environmental, health, and safety compliance. Job Qualifications
Education: Bachelor’s degree (B.A./B.S.) or equivalent in a life science (biology, chemistry), environmental engineering, or related discipline. Experience: Ten to 15 years related experience in a regulated environment. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above. Certification/Licensure: Preferred but not required: CSP, CIH, and/or other EHS credential. The pay range for this position is $145,700 - $161,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. About Charles River’s CDMO Services
With over 20 years of experience and industry-leading expertise, Charles River’s cell and gene therapy Contract Development and Manufacturing Organization (CDMO) group supports biotechnology and pharmaceutical companies in advancing their complex programs from early development through commercialization. Our integrated, phase-appropriate CDMO capabilities—including plasmid DNA, viral vector, and cell therapy manufacturing—enable seamless development and faster timelines. With centers of excellence in the US and UK, we offer GMP-compliant and research-grade solutions, along with comprehensive analytical services and regulatory support. Whether clients need end-to-end development, standalone services, or insourced support, our CDMO team provides custom solutions to meet evolving program needs. From process development in Hanover to viral vector manufacturing in Rockville, large-scale cell therapy production in Memphis, and plasmid DNA services in Keele, we simplify the supply chain and accelerate cell and gene therapy breakthroughs. About Charles River
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.
#J-18808-Ljbffr