Technician I Methods Development

For 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.

Job Summary

SUMMARY

Under direct supervision, performs technical laboratory activities in support of client studies or procedures. Performs analysis of data for quality and completeness and determines if results are as expected. Records data in compliance with company and regulatory policies and standards to meet quality and accuracy requirements.

 

ESSENTIAL DUTIES AND RESPONSIBILITIES:

  • Prepare reagents including buffers, chemical solutions,protein soultions, complex reaction mixtures and media preparation according to standard test methods and standard operating procedures.
  • Perform tasks using aseptic techniques including working within a biological safety cabinet.
  • Participate in the general maintenance of all equipment related to the preparation of assay materials and the analysis of samples, and schedule repairs as required.  Perform any laboratory maintenance and/or monitoring as necessary.
  • Perform a variety of molecular and cell biology laboratory experiments, tests and procedures following well-defined techniques and guidelines, including isolation and analysis of DNA, RNA, and proteins, PCR, RT-PCR, ELISA, cell growth..
  • Conduct aseptic growth and manipulation of bacteria, virus and mammalian cells.
  • Make detailed observations and accurately and precisely record data.  Summarize data for reports; perform simple graphic analysis of data. Document all activities performed in notebooks and test batch records in accordance with the current Good Manufacturing Practices.
  • Report results of experiments, tests and procedures, and analyze data.
  • Efficiently organize and plan daily activities.
  • Maintain a safe working environment by adhering to company policies and procedures.
  • Follow all SOPs, STMs and cGMP and cGLP guidelines as they relate to specific tasks.
  • Perform all other related duties as assigned

 

QUALIFICATIONS:

  • Education:Bachelor’s degree (B.S.) or equivalentinbiology or related discipline.
  • Experience:0 to 1 year of related experience in a biological laboratory.  Knowledge of basic molecular biology techniques or other analytical testing required.
  • 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:Knowledge of cGMPs or regulatory affairs pertaining to the pharmaceutical and biological industries is preferred. Must possess excellent interpersonal skills to maintain communication across biological functional groups.Able to communicate effectively in a group or one on one setting.  Basic Microsoft Office skills are a plus. 

 

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 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

 

Company
CHARLES RIVER LABORATORIES
Posted
06/23/2018
Type
Full time
Location
Malvern, PA 19355, US