Formulations Technician I:
Charles River Laboratories

28544-en_US
Charles River Laboratories
Shrewsbury Massachusetts
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 we perform. In return, we’ll help you build a career that you can feel passionate about.

We are seeking an experienced Formulations Technician I for our Safety Assessment site located in Shrewsbury, MA.   

 

Under supervision, participate in the receipt, handling, use and disposition of test articles, including food additives, drugs and medical devices for use in simple non-clinical test studies.  Responsible for study set-up and assisting other technicians in formulation procedures.  Perform basic formulation procedures consistent with study protocols, SOPs and any applicable regulations.

 

The following are minimum requirements related to the Formulations Technician I position:

  • Education:  Associate's degree (AA/AS) or equivalent in a Life Science, Chemistry or related discipline.  Bachelor's degree (B.A./B.S.) preferred. 
  • Experience:  0 to 1 years related experience in a contract, chemistry or biotechnology laboratory setting, including experience with Pharmacy related research and investigative procedures and techniques or a related discipline.  
  • An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
  • Certification/Licensure:  None.
  • Other: Basic knowledge of GLP preferred.  GLP requires attention to detail, strong organizational skills and accurate record keeping competencies.  A mathematical aptitude is required.

 

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.


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

Basic Qualifications
Requirement