Manager, Technical Operations:
Charles River Laboratories

29042-en_US
Charles River Laboratories
Reno Nevada
Biotech
Description

For nearly 70 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 e perform. In return, we’ll help you build a career that you can feel passionate about.


Responsibilities

We are seeking an experienced Manager, Technical Operations for our Safety Assessment site located in Reno, Nevada

In addition to study-related responsibilities, provides leadership and management to the Technical Operations Department. This position is responsible for oversight of Study Supervisors and/or Lab Assistant Group Leader, for reviewing operational SOP's, and for recruitment of staff within each research team.

The following are minimum requirements related to the Manager, Technical Operations position.

  • Bachelors degree (B.A./B.S.) or equivalent in scientific related discipline.
  • 2 years related technical experience in laboratory and/or animal research.
  • 2 years management experience in a nonclinical GLP laboratory.
  • An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
  • LAT required, LATg preferred.
  • Must be computer literate in standard office software and must be able to perform all functions requried of the Senior Study Supervisor.

 

About Safety Assessment Business

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 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

Salary Grade: 86


Who May Apply

The policy of Charles River Laboratories is to provide advancement opportunities to all qualified employees within the company through transfers or promotions.
Regular Full and Part Time employees may apply for a Job Posting if they meet the eligibility requirements set forth in the Internal Job Posting policy.
Regular Full and Part Time Employees must complete at least one year of continuous active service in their position prior to applying.
Regular Full and Part Time Employees are eligible to participate in the Job Posting Process if their current overall performance appraisal rating is equivalent to "satisfactory" or better.
Regular Full and Part Time Employees cannot be in any stage of a disciplinary action.
Regular Full and Part Time Employees on leave of absence are not eligible to apply.

 

 

 

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 120 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 11,000 employees within 70 facilities in 18 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. And in 2016, revenue increased by 23.3% to $1.68 billion from $1.36 billion in 2015. 

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 ~70% of the drugs approved by the FDA in 2016.

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

 

Equal Employment Opportunity

 

Charles River Laboratories, Inc. is an Equal Opportunity Employer M/F/Disabled/Vet

Basic Qualifications
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