Scientist 1 Methods Development

Req ID #:  45412

Malvern, PA, US

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

Assist in the development of methods for biopharmaceutical services testing. Under minimal supervision, may be responsible for method development, client interaction, interpretation and reporting of data and regulatory compliance of assigned research projects.


We are seeking a Scientist I for our Biologics Testing Solutions site located in Malvern, PA.

Job Responsibilities
  • Plan and execute laboratory research for biopharmaceutical services testing.
  • Participate in activities such as RNA isolation, DNA isolation, DNA cloning, DNA sequencing, PCR and other standard molecular biology techniques.
  • Use sequence analysis tools and DNA sequence databases to generate oligonucleotide primers and probes for PCR assay development.
  • Review, interpret, integrate and present experimental data using assistance of senior technical staff as appropriate.
  • Generate high-quality protocols and reports in conjunction with senior research personnel.


The following are minimum requirements related to the Scientist 1 position:

  • Education: Doctoral degree (Ph.D.) or equivalent in a scientific discipline related to molecular biology.
  • Experience: Minimum of 0-3 years’ experience in a biological research and/or development environment.
  • An equivalent combination of education and experience with contract research or the pharmaceutical industry may be accepted as a satisfactory substitute for the specific education and experience listed above.
  • Other: Ability to work on problems of moderate scope where analysis of situation or data requires a review of identifiable factors. Exercises judgment within defined procedures and practices to determine appropriate action. Demonstrates potential for technical proficiency, scientific creativity, and collaboration with others and independent thought. Effective written and verbal communication skills with the ability to handle multiple projects, prioritize work and meet deadlines within a GMP environment. Capable of data interpretation of basic molecular biology

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 14,000 employees within 80 facilities in 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. And in 2018, revenue increased by 22% to $2.27 billion from $1.86 billion in 2017.


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 ~85% of the drugs approved by the FDA in 2018.


Equal Employment Opportunity 


Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet




Nearest Major Market: Philadelphia

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