Supervisor Manufacturing Training

Req ID #:  200043
Location: 

Memphis, TN, US, 38118 Memphis, TN, US, 38118

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.


IMPORTANT:   In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process.  Please make sure work history and education are added correctly. 

Job Summary

Manage the development, implementation, and sustainability of manufacturing training activities in accordance with cGMPs, internal Quality Management System and process documents. Oversees manufacturing trainers in execution of training. Assures reports understand duties, responsibilities, policies, and procedures. Lead, mentor and develop reports. Monitors the effectiveness of training and continuously improves programs. Develops new training programs to support change management. Committed to expanding personal knowledge and expertise as industry develops. Provides assistance to management in the writing and revision of process documents.

 

  • Execute GxP training strategies through determining priority and achieving learning objectives through high quality, innovative, timely and effective learning solutions
  • Develop training resources within manufacturing dept that can be leveraged across the site and align with internal Learning Management Systems
  • Assess and improve training strategies and tools
  • Maintain and improve onboarding experience for manufacturing hires
  • Provide guidance and information to leadership in regards to recommending training programs, curricula and training material development
  • Support policy and procedural changes to improve the quality of the department. Evaluate and report on effectiveness of changes
  • Collaborate across departments to develop and oversee departmental strategy and goals in alignment with site goals
  • Demonstrate CRL DNA behaviors
  • Lead, mentor and develop direct reports

Job Qualifications

  • 3 to 5 years in a GxP environment is preferred
  • Knowledge of Learning Management Systems
  • Excellent communication and interpersonal skills
  • Strong capability for logical and analytical thinking
  • Must be detail oriented with excellent organizational skills
  • Previous supervisory or management level experience is preferred
  • Demonstrated ability to work with others in a multicultural environment
  • Multi-disciplinary knowledge of biotech or cellular manufacturing industry preferred

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV. 


Vaccine Mandate
Charles River is a U.S. Federal Contractor.  As a result, we must follow the Presidential Executive Order to mandate vaccinations, and ensure our employees are fully vaccinated against COVID-19.  Our main priority is the wellbeing, health, and safety of our people. We require proof of vaccination from all employees. 


Anyone with requests for disability-related and/or religious exemptions should contact Talent Acquisition (crrecruitment_US@crl.com) so that information can be provided about the accommodation process at Charles River.

 

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 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 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.
  


Nearest Major Market: Memphis

Job Segment: Pharmaceutical, Recruiting, Laboratory, Training, Biotech, Science, Human Resources, Operations