Deputy Program Manager

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Deputy Program Manager

Charles River Laboratories, Inc.

icon Bethesda, MD, US, 20892

icon10 July 2024

Job Expired

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

We are looking for a Deputy Program Manager to join our Insourcing Solutions team, located in Bethesda, MD. 

How will you have an impact? 

This is the moment to use your talents and imagine those talents contributing to improving global health and peoples’ lives. In the DPM role, you can do that by supervising personnel and operations to maintain a high standard of performance to a large multi-species and multi-position contract for the National Institute for Allergy and Infectious Disease, which directly contributes to the integrity of the research.  

Why work at Charles River?  

We offer an excellent onboarding program for our new employees, internal career development, and competitive benefits!  

What you will do! 

In the Deputy Program Manager role, you will use existing SOPs and quality assurance standards to oversee the operations and a staff of animal care supervisors, research support staff, veterinary and animal care technicians, and animal facility attendants for a multi facility contract. Conduct training activities, participate in supervisory activities such as recruitment, separation, performance appraisals, disciplinary actions, and employee programs/activities. You will interact with client representatives to resolve various inquiries and participate in the development of projections for equipment, supplies, and personnel needed to effectively operate the research facilities. You will assist facility managers and staff to establish specifications for recommendations for the selection and purchase of animal care related equipment; as well as develop, review, and write site specific standard operating procedures for the care of laboratory animals, and the operation of the facility. You will also assist in the review and analysis of operational needs and make recommendations to enhance the efficiency and effectiveness of animal care services. 

continued

In this role, you will act as corporate liaison to designated contract business clients to assess contract performance; supervise record maintenance, generate external/internal reports, and prepare/submit records, charts, logs, and inventories. You will serve as temporary backfill for Facility Managers during vacancies and assist them with ensuring that animal care staff perform all tasks at or above standards. There will be a need to conduct periodic meetings with subordinate staff to keep them informed of current and future projects, policies, and procedures; as well as assist in assessing training needs, including developing and presenting training for staff and investigators, developing course content and materials for training and continuing education of the animal care staff to achieve AALAS certification. In addition, investigate personnel problems and develop performance improvement plans, provide counseling to employees, and write employee performance evaluations. Periodically, you may be asked to review site quality assurance procedures for various functions within the facility such as animal health surveillance, cagewash/autoclaves, animal shipments, and the HVAC. 

Job Qualifications

A candidate that possesses either a BS degree in Animal Sciences or Biological Sciences is preferred, HSD required. Has at least 8 years’ experience working in a large complex animal program, 4 years of which shall have been in a supervisory capacity. Experience in specialty areas, such as rodent and rabbit facilities management, NHP (Non-Human Primate) facilities management, barrier management, hazard containment, and animal facility date management are needed. Must be LATG (Laboratory Animal Technologist) certified; preference given to CMAR certification. 

About Insourcing Solutions
Charles River Insourcing Solutions℠ can streamline research by delivering operational and cost efficiencies through the strategic insourcing of GMP, GLP and non-GLP research services from discovery through safety assessment. Insourcing Solutions℠ provides you with the ability to maintain control of your facility and expertise while leveraging available space.


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, 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.

For more information, please visit www.criver.com.

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